4.1.1 Flashcards

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1
Q

What are the four types of pathogen?

A
  • Bacteria
  • viruses
  • protoctista (Protista)
  • Fungi
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2
Q

Which type of bacteria causes communicable diseases?

A

Pathogens

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3
Q

What are the two ways that bacteria can be classified?

A
  • Basic shapes

- cell walls

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4
Q

How can bacteria be classified by their basic shape?

A
  • Rod shaped (bacilli)
  • spherical (cocci)
  • comma shaped (vibrios)
  • spiralled (spirilla)
  • corkscrew (spirochaetes)
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5
Q

How can bacteria be identified by their cell walls?

A

Two types:

  • gram-positive bacteria: blue/purple under light microscope (Staphylococcus aureus MRSA)
  • gram-negative bacteria: red (e.coli)
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6
Q

Why is knowing the type of cell wall of a bacteria useful?

A

Because it affects how bacteria reacts to different antibiotics

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7
Q

What is an antibiotic?

A

Compound that kills or inhibits the growth of bacteria

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8
Q

What is a virus? What is the structure of the virus?

A
  • Nonliving infectious agents

- some genetic material surrounded by protein

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9
Q

How do viruses cause communicable diseases?

A

Invade living cells
Take over biochemistry of the host cell to make more viruses
Reproduce rapidly and evolve by developing adaptations to the host (successful pathogens)

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10
Q

What are the viruses that attack bacteria?

A

Bacteriophages

They take over bacterial cells and use them to replicate whilst destroying the bacteria

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11
Q

What is protoctista?

A

Eukaryotic organisms with a wide variety of feeding methods

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12
Q

What do protoctista cause?

A

Parasitic diseases that use people/animals as a host

May need a vector to transfer them to the host

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13
Q

What is fungi?

A

Eukaryotic organisms that are mostly multicellular

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14
Q

What do fungi do to an organism?

A

-They feed on dead or decaying matter but some are parasitic so can feed on living organisms

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15
Q

How can fungi kill a plant?

A

Often infect plant leaves, stopping them from photosynthesising, quickly killing the plant

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16
Q

How can fungi spread between organisms?

A

They produce millions of tiny spores that can spread Widely through crop plants
Can cause hardship and starvation

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17
Q

How do viruses take over? 6 steps

A
  1. Virus attaches to host cell
  2. It inserts viral nucleic acid (Genetic material)
  3. The viral nucleic acid replicates
  4. The synthesis of the viral protein happens
  5. Then the assembly of the virus particles
  6. Lysis of the host cell, allowing the new viruses to spread to infect other cells
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18
Q

How do protoctista take over a cell?

A

They digest and use the cells contents to reproduce

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19
Q

What can bacteria produce and what does this do?

A
Toxins (poison/damage host cells)
-breakdown cell membranes
-Damage/inactivates enzymes
-interfere with host so genetic material
Toxins or a byproduct of the normal functioning of the bacteria
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20
Q

How do plant diseases threaten people?

A

When crops fail…

  • people can starve
  • economies can struggle
  • ecosystems are threatened as well
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21
Q

What is ring rot?

A

Bacterial disease
(potatoes tomatoes aubergines)
Damages leaves, tubers, fruit and can destroy up to 80% of the crop
No cure

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22
Q

What is tobacco mosaic virus?

A

Infects tobacco plants and around 150 other species
Damages leaves, flowers, fruit (Stunts growth, reducing yield)
No cure
There are resistant crop strains

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23
Q

What is potato blight?

A

Fungus-like protoctista
Penetrates host cells, destroys leaves/tubers/fruits
No cure
There are resistant strains
(Careful management, chemical treatments can reduce infection risk)

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24
Q

What is black Sigatoka?

A

Fungus
Attacks and destroys leaves
Fungicide treatments can control the spread
No Cure

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25
Q

What is tuberculosis?

A

Bacterial disease
Destroys lung tissue and suppresses the immune system (body is less able to fight off other diseases)
Curable with antibiotics
Preventable with a vaccination and improving living standards

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26
Q

What is bacterial meningitis?

A

Starts at brain and can spread to the rest of the body causing septicaemia
Antibiotics can cure it if delivered early
Vaccines can protect against some forms of bacterial meningitis

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27
Q

What is HIV/AIDS?

A

AIDS is caused by HIV, targets T-helper cells in the immune system so it’s gradually destroys it
People with HIV are more likely to get other infections (TB) and some types of cancer
It has the enzyme reverse transcriptase that transcribes RNA to single strand of DNA to produce a single strand of DNA in host cell.
Passed by bodily fluids
Anti retroviral drugs slow the progress of the disease

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28
Q

What is influenza?

A

Virus
Kills the ciliated epithelium cells in the gas exchange system (airway open to secondary infection)
Most deaths off from the secondary bacterial infection (pneumonia)
Having flu one year leaves you with some immunity for the next but it mutates regularly

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29
Q

What is malaria?

A
Protoctista 
Has two hosts: Mosquitoes and people
Invades red blood cells, liver, brain making people weak and vulnerable to other infections
No vaccine and limited cures
Control the vector (prevent mosquitoes)
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30
Q

What is Ring worm?

A

Fungus
Causes grey white crusty infectious circular area of skin (itchy)
Antifungal cream can cure it

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31
Q

What is athletes foot?

A

Fungal disease
Grows on and Digests warm moist skin between toes
Crackling and scaling (itchy)
Antifungal cream can cure it

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32
Q

What are five different ways of direct Transmission?

A
  • Kissing or contact with bodily fluids
  • skin to skin contact
  • microorganisms from faeces transmitted on hands
  • Inoculation
  • ingestion
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33
Q

How does transmission through inoculation happen?

A

-Break in the skin
– animal bites
– puncture wound or through sharing needles

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34
Q

How does transmission through ingestion happen?

A
  • Consuming contaminated food or drink

- transferring pathogens from hand to mouth

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35
Q

What are three ways of indirect transmission?

A
  • Formites
  • droplet infection (inhalation)
  • vectors
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36
Q

What are formites and how do they transmit diseases?

A

-Inanimate objects that can transfer pathogens

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37
Q

How does droplet infection transmit diseases?

A

Small droplets of saliva and mucus are expelled they can contain pathogens
Healthy individual may breathe them in and become infected

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38
Q

How do vectors transmit diseases?

A

From one house to another
Are often animals (e.g. mosquitoes)
Water can also act as a vector (e.g. diarrhoeal diseases)
People can be vectors for animal diseases (foot and mouth disease)

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39
Q

What is environmental factors can cause the transmission of communicable disease in animals? Mention 7

A
  • Overcrowded living/working conditions
  • poor nutrition
  • compromised immune system/immunosuppressant drugs after transplant
  • poor disposal of waste
  • climate change (new vectors and new diseases), (high temperatures promote spread of malaria)
  • culture and infrastructure (traditional medical practices)
  • Socio- economic factors (lack of trained health workers, insufficient public warning during outbreak)
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40
Q

How does direct transmission happen between plants?

A

Healthy plant with any part of the disease plant

e.g. ring rot, tobacco mosaic virus, tomato and potato blight, black sigatoka

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41
Q

What are two ways of indirect transmission in plants?

A
  • Soil contamination

- vectors

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42
Q

How does soil contamination cause indirect transmission of communicable diseases?

A

Infected plants leave pathogens or reproductive spores in the soil that can infect the next crop

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43
Q

What are the four types of vectors and how do they cause indirect transmission of communicable diseases in plants?

A
  • wind: spores may be carried
  • Water: spores swim in surface film of water on leaves
  • animals: carry Pathogens and spores from one plant to another as they feed
  • humans: pathogens and spores transmitted by hand, clothing,formites
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44
Q

What environmental factors affect the transmission of communicable diseases in plants? Name 5

A
  • Planting variety of crops susceptible to disease
  • overcrowding increases spread
  • poor mineral nutrition reduce resistance
  • damp and warm conditions increase survival
  • climate change (allow animal vectors to spread) (increased rainfall and went to promote spread)
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45
Q

How do plants respond to an attack (vaguely)?

A

Chemical is produced when the cell wall is attacked
Release of signalling molecules
Triggers cellular responses (defensive chemicals)
These chemicals send alarm signals to unaffected cells to trigger the defences and physically strengthens the cell wall

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46
Q

What polysaccharide is produced when a plant recognises an attack?

A

Callose

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47
Q

What is the role of callose in plant defence?

A
  • It is deposited between cell walls and cell membrane next to infected cells, they act as barriers preventing the pathogens from entering
  • large amounts continue to be deposited after initial infection, lignin is added making the mechanical barrier thicker and stronger
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48
Q

Where is callose deposited and what does this do?

A
  • Blocks sieve plates in flooring: sealing infected part, preventing spread
  • Deposited in plasma does matter between infected cells and neighbours sealing them off from healthy cells to prevent spread
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49
Q

What is chemical defences can be used to prevent the spread of communicable diseases in plant?

A
  • Insect repellent
  • insecticides
  • anti bacterial compounds (antibiotics) phenols
  • Antifungal compounds (interfere with fungal cell membranes (chitinases -breaks down chitin in fungal wall)
  • Anti-oomycetes (glucanases-Breakdown glucans (polymers found in cell walls of oomycetes)
  • General toxins (made by plants)
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50
Q

How does skin keep pathogens out?

A
  • Covers body preventing entry
  • skin flora of healthy microorganisms: outcompete pathogens for space on surface
  • sebum oily substance that inhibits the growth of pathogen
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51
Q

What adaptation in the airways keeps pathogens out?

A

Mucous membranes that secrete mucus (traps microorganisms, contains lysozymes)
Mucus has phagocytes that remove remaining pathogens

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52
Q

What do lysozymes do and where else can they be found?

A

Destroy bacterial and fungal cell walls

Tears and urine

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53
Q

What are expulsive reflexes and how do they keep pathogens out?

A

Coughs/sneezes eject pathogen leading mucus

Vomiting/diarrhoea expel contents of gut along with infective pathogens

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54
Q

How does blood clot?

A

Platelets come into contact with collagen and skin/wall of the damaged blood vessel and they secrete several substances

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55
Q

What substances do platelets secrete to help with blood clot?

A

Thromboplastin: enzyme that triggers a cascade of reactions resulting in the formation of blood clot
Serotonin: make smooth-muscle in the walls of blood vessels contract (reducing supply of blood to the area)

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56
Q

What happens after the clutch dries out and formed a tough scab?

A

Epidermal cells start to grow under the scab sealing the wound permanently,
Damaged blood vessels regrow
Collagen fibres are deposited to give new tissue strength
Once the new epidermis reaches normal thickness, scab falls off and the wound is healed

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57
Q

How is inflammation characterised?

A

Pain
Heat
Redness
Swelling

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58
Q

Describe the inflammatory response?

A

Mast cells are activated in damaged tissue, they release chemicals: histamines, cytokines
Histamines: make blood vessels dilate (localised heat and redness) raised temperature prevents pathogens reproducing
They also make blood vessels more leaky so blood plasma is forced out this tissue fluid causes swelling (oedema) and pain
Cytokines: attracts white blood cells that carry out phagocytosis

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59
Q

What are non-specific defences give two examples (animals)?

A

Fever

Phagocytosis

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60
Q

How does fever get rid of pathogens?

A

Cytokine stimulates hypothalamus to reset thermostat (temperature increases)

  • Pathogens reproduce best at or below 37°C, high temps inhibit reproduction
  • specific immune system works faster at higher temperatures
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61
Q

What are Phagocytes? and what are the two main types?

A

Specialised white cells that engulf and destroy pathogens

Neutrophils, macrophages

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62
Q

Describe the five stages of phagocytosis

A
  1. Pathogen is produce chemicals that attracts phagocytes
  2. Phagocytes recognises nonhuman proteins on pathogen (antigen) the response is not specific it’s simply to a cell or an organism that is non-self
  3. Phagocyte engulfs the pathogen and encloses it in a vacuole: phagosome
  4. phagosome combines with lysosome: phagolysosome
  5. Enzymes from the lysosome digest and destroy the pathogen
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63
Q

Why do macrophages take longer to destroy bacteria?

A

It’s combines antigens from the pathogen surface membrane with special glycoproteins in the cytoplasm called major histocompatibility complex (MHC)
MHC complex moves pathogen antigens to macrophages surface membrane: antigen-presenting cell

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64
Q

What can the antigen-presenting cell do?

A

Stimulate other cells involved in the specific immune system response

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65
Q

What are the three functions of cytokines?

A

Act as cell signalling molecules
Increased body temperature
Stimulate the specific immune system

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66
Q

What are opsonins?

A

Chemicals that bind to pathogens and “Tag “them so they can be more easily recognised by phagocytes

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67
Q

What happens during inflammation?

A

Mast cells are activated

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68
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

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69
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

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70
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

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71
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
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72
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

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73
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

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74
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
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75
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
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76
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

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77
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

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78
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
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79
Q

What do you B plasma cells do?

A

They produce many antibodies

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80
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
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81
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

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82
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

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83
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

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84
Q

What happens during inflammation?

A

Mast cells are activated

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85
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

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86
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

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87
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

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88
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
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89
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

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90
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

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91
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
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92
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
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93
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

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94
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

How well did you know this?
1
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95
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
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96
Q

What do you B plasma cells do?

A

They produce many antibodies

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97
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
How well did you know this?
1
Not at all
2
3
4
5
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98
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

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99
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

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100
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

How well did you know this?
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101
Q

What happens during inflammation?

A

Mast cells are activated

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102
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
103
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

How well did you know this?
1
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104
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

How well did you know this?
1
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105
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
How well did you know this?
1
Not at all
2
3
4
5
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106
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

How well did you know this?
1
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107
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

How well did you know this?
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108
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
How well did you know this?
1
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2
3
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109
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
How well did you know this?
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110
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

How well did you know this?
1
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2
3
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5
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111
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
112
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
How well did you know this?
1
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113
Q

What do you B plasma cells do?

A

They produce many antibodies

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114
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
115
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

How well did you know this?
1
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2
3
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5
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116
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

How well did you know this?
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2
3
4
5
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117
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

How well did you know this?
1
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2
3
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5
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118
Q

What happens during inflammation?

A

Mast cells are activated

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3
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119
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
120
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
121
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

How well did you know this?
1
Not at all
2
3
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5
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122
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
123
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

How well did you know this?
1
Not at all
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124
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

How well did you know this?
1
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2
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125
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
126
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
How well did you know this?
1
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127
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
128
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
129
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
How well did you know this?
1
Not at all
2
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5
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130
Q

What do you B plasma cells do?

A

They produce many antibodies

How well did you know this?
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2
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131
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
132
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
133
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
134
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
135
Q

What happens during inflammation?

A

Mast cells are activated

How well did you know this?
1
Not at all
2
3
4
5
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136
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
137
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
138
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
139
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
140
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
141
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
142
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
143
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
144
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
145
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
146
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
147
Q

What do you B plasma cells do?

A

They produce many antibodies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
148
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
149
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
150
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
151
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
152
Q

What happens during inflammation?

A

Mast cells are activated

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
153
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
154
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
155
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
156
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
157
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
158
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
159
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
160
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
161
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
162
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
163
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
164
Q

What do you B plasma cells do?

A

They produce many antibodies

165
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
166
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

167
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

168
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

169
Q

What happens during inflammation?

A

Mast cells are activated

170
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

171
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

172
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

173
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
174
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

175
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

176
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
177
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
178
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

179
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

180
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
181
Q

What do you B plasma cells do?

A

They produce many antibodies

182
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
183
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

184
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

185
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

186
Q

What happens during inflammation?

A

Mast cells are activated

187
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

188
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

189
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

190
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
191
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

192
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

193
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
194
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
195
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

196
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

197
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
198
Q

What do you B plasma cells do?

A

They produce many antibodies

199
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
200
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

201
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

202
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

203
Q

What happens during inflammation?

A

Mast cells are activated

204
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

205
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

206
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

207
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
208
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

209
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

210
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
211
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
212
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

213
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

214
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
215
Q

What do you B plasma cells do?

A

They produce many antibodies

216
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
217
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

218
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

219
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

220
Q

What happens during inflammation?

A

Mast cells are activated

221
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

222
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

223
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

224
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
225
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

226
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

227
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
228
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
229
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

230
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

231
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
232
Q

What do you B plasma cells do?

A

They produce many antibodies

233
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
234
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

235
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

236
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

237
Q

What happens during inflammation?

A

Mast cells are activated

238
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

239
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

240
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

241
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
242
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

243
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

244
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
245
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
246
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

247
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

248
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
249
Q

What do you B plasma cells do?

A

They produce many antibodies

250
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
251
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

252
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

253
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

254
Q

What happens during inflammation?

A

Mast cells are activated

255
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

256
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

257
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

258
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
259
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

260
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

261
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
262
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
263
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

264
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

265
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
266
Q

What do you B plasma cells do?

A

They produce many antibodies

267
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
268
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

269
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

270
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

271
Q

What happens during inflammation?

A

Mast cells are activated

272
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

273
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

274
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

275
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
276
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

277
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

278
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
279
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
280
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

281
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

282
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
283
Q

What do you B plasma cells do?

A

They produce many antibodies

284
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
285
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

286
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

287
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

288
Q

What happens during inflammation?

A

Mast cells are activated

289
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

290
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

291
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

292
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
293
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

294
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

295
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
296
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
297
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

298
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

299
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
300
Q

What do you B plasma cells do?

A

They produce many antibodies

301
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
302
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

303
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

304
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

305
Q

What happens during inflammation?

A

Mast cells are activated

306
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

307
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

308
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

309
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
310
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

311
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

312
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
313
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
314
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

315
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

316
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
317
Q

What do you B plasma cells do?

A

They produce many antibodies

318
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
319
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

320
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

321
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

322
Q

What happens during inflammation?

A

Mast cells are activated

323
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

324
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

325
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

326
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
327
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

328
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

329
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
330
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
331
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

332
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

333
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
334
Q

What do you B plasma cells do?

A

They produce many antibodies

335
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
336
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

337
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

338
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

339
Q

What happens during inflammation?

A

Mast cells are activated

340
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

341
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

342
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

343
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
344
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

345
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

346
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
347
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
348
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

349
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

350
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
351
Q

What do you B plasma cells do?

A

They produce many antibodies

352
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
353
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

354
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

355
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

356
Q

What happens during inflammation?

A

Mast cells are activated

357
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

358
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

359
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

360
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
361
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

362
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

363
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
364
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
365
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

366
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

367
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
368
Q

What do you B plasma cells do?

A

They produce many antibodies

369
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
370
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

371
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

372
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

373
Q

What happens during inflammation?

A

Mast cells are activated

374
Q

What two chemicals do mast cells release? What do each of these chemicals do?

A

Histamines:
-dilates blood vessels (local heat and redness: slows pathogen reproduction)
-more leaky blood vessels (Swelling and pain:more tissue fluid so more neutrophils leave due to lobed nucleus)
Cytokines: cell signalling, attract phagocytes leading to phagocytosis

375
Q

What is the difference between a neutrophil and a macrophage?

A

N: lobed nucleus, can leave the blood stream
M: round nucleus, can’t leave blood stream, has major histocompatibility complex

376
Q

What is MHC responsible for?

A

It is the protein that turns the macrophage into an antigen presenting cell

377
Q

What are the steps of a macrophage becoming an antigen presenting cell?

A
  • macrophage engulfs pathogen
  • phagosome is formed
  • Phagosome fuses with lysosome making a phagolysosome, Lysosome digests the pathogen except for the antigens
  • antigen and MHC combine, placed on the surface making APC
378
Q

What is the difference between T lymphocytes and B lymphocytes?

A

T: made in bone marrow, mature in thalamus gland
B: made and matured in bone marrow (can become APC)

379
Q

How is the T-helper cell activated?

A

CD4 Receptor recognises the antigen MHC complex

380
Q

What does the T-helper cell do?

A
  • Releases interleukins that trigger mitosis and specialisation of cells
  • signals B cells to work
381
Q

After mitosis of T-helper cells what can be produced?

A
  • T memory cells
  • T killer cells
  • T regulatory cells
382
Q

What do you T killer cells do?

A

Release perforin or H202 (Hydrogen peroxide)

They kill cells

383
Q

What T regulatory cells do?

A

Suppresses immune system by killing all white blood cells except for T memory and B memory.
To prevent autoimmunity

384
Q

Describe the humoural response

A
  1. Clonal selection: choosing the right B-cell (B-effector cells make different antibodies) that is complimentary to the pathogen
  2. Clonal expansion where the B antigen-presenting cells divide by mitosis to make B memory cells or B plasma cells
385
Q

What do you B plasma cells do?

A

They produce many antibodies

386
Q

What are the four things that immunoglobin can become?

A
  • They can directly attack
  • agglutinins
  • opsonins
  • antitoxins
387
Q

What do agglutinins do?

A

They glue in different pathogen is making a big batch

Easier to catch

388
Q

What do antitoxins do?

A

Neutralise toxins released by pathogens

389
Q

What do you T memory and B memory cells do

A

Immunological memory

Used in the secondary response so that if encountering the same pathogen is it can go straight to specific response

390
Q

What happens during inflammation?

A

Mast cells are activated

391
Q

What is an autoimmune disease?

A

Immune system stops recognising self cells and attacks healthy body tissue

392
Q

What is a treatment for autoimmune diseases?

A

Immunosuppressant drugs
-prevent immune system working
But deprive the body of natural defences against communicable diseases

393
Q

Give three examples of autoimmune diseases

A

Type one diabetes
Rheumatoid arthritis
Lupus

394
Q

What is natural active immunity?

A

When the body acts to produce antibodies or memory cells

395
Q

Where does the newborn baby get his antibodies from?

A
  • Some cross the placenta from the mother

- first mammilian milk (colostrum) is high in antibodies

396
Q

What is natural passive immunity?

A

When the body gets his immunity from somewhere else before it starts making his own (in newborn babies)

397
Q

What is artificial passive immunity?

A

Antibodies from one individual extracted and injected into the bloodstream of another (temporary)

398
Q

What is artificial active immunity?

A

Using the safe form of an antigen (a vaccine)

399
Q

How can pathogens be made safe to act as vaccines?

A
  • Bacteria/viruses are killed or inactivated
  • weakened strains of the live bacteria or virus
  • toxin molecules have been altered and detoxified
  • isolated antigen is extracted from pathogen
  • genetically engineered antigens
400
Q

What is an epidemic?

A

Communicable disease spreads rapidly to all people at a local or national level

401
Q

What is a pandemic?

A

Same disease spreads rapidly across a number of countries and continents

402
Q

What is a herd immunity?

A

Enough people in the population have been vaccinated and it protects those who don’t have immunity

403
Q

What is personalised medicine?

A

Combination of drugs that work with individual combination of genetics and disease

404
Q

What is pharmacogenomics?

A

Science of interweaving knowledge of drug actions with personal genetic material

405
Q

What is the MRSA?

A

Methicillin resistant staphylococcus aureus

  • 30% of population have it on skin or nose
  • causes boils abscesses fatal septicaemia
  • was treated with methicillin but mutation causes resistance resistant strains
406
Q

What is C. difficile?

A

Clostridium difficile

  • guts in 5% of population
  • toxins that damage lining of intestines, diarrhoea bleeding and death
  • kills off healthy gut bacteria