Body protection against infections Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

Bacterial effects on body

A

1. Production of toxins - poisonous substances (metabolic wastes) that alters chemical reactions/affects cell function
2. Injury to cells and tissues - bacteria bore through cell walls/membrane, so there is leakage/fluid loss. Pathogens feed on some types of body cells.
3. Bacterial numbers - put pressure on surrounding organs, causing disruptions

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

Viruses

A

non-living - they have no organelles.
Must infect a living host cell to replicate/survive. They take over host cell’s metabolism.
cant survive long outside of host.
Viruses are specific in the types of cells they infect.

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

viral replication

A

1. Virus attaches to outside of host cell - it’s surface proteins (spikes) must attach to specific receptor sites on host cell surface.
2. Uncoated RNA enters lymphocyte
3. Viral RNA (the template) is made into viral ‘DNA’ using a viral enzyme
4. Host cell DNA in nucleus then integrates the viral DNA into its chromosomes
5. The viral genes are now transcribed into mRNA strand.
6. Viral mRNA is translated at the ribosomes into HIV proteins - generating new virus particles

Budding of new viruses (100’s) from host cell or new viruses are released by lysis/rupturing the host cell.

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

structural characteristics of bacteria

A

Microscopic, unicellular organism
outer cell wall, no membrane bound organelles
Prokaryote - has no nucleus, free floating or rings of DNA - plasmid
presence of flagellum
Classified according to shape

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

bacteriophage

A

Viruses which attack bacterial cells.
they multiply in bacterial cells causing lysis (breaking)/death of the host bacterium.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Structural characteristics of Viruses

A

seen using electron microscope
Classified according to their nucleic acid
Caspid (head) wt DNA or RNA - surrounded by taking over host cell’s DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Protozoa

A

microscopic, single celled organisms
Passed on by drinking infected water

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

fungi

A

Typically affects the skin, and mucous membranes
yeast, moulds, mushrooms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Ways of transmission of vectors

A

1. Transmission by contact - direct contact, actually touching an infects person. Indirect contact - touching an object that has been touched by an infected person.
2. Ingestion of food or drink - contaminated wt pathogens
3. Transfer of body fluids - when infected blood, saliva, semen -body fluids- come in contact with mucous membranes -nose, mouth, throat, genitals or blood stream.
4. Infection by droplets - pathogens in tiny droplets of moisture emitted when infected person breathes, talks, sneezes, coughs, sending infectious drops into air (the breathed in) or may settle on food or ustensils or eaten later. (Short range transmission)
5. Airborne transmission - when moisture in exhaled droplets evaporates - some bacteria and virus remain viable and can cause infection
6. Transmission by vectors - transfer of pathogens by animals: fly, insects, mosquitoes, fleas. Vectors are carriers of a disease (not affected by disease that they carry). An intermediate host of the pathogen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Inflammatory response

A

body’s 2nd line of defence
Protective response of body (non-specific)
inflammation is a response that occurs when tissue is damaged; involves swelling, heat, pain + redness in affected areas.
Damage to the skin by heat/burns, chemicals, mechanical injury: cut, piercing with pin, infection, eg. Skin, scratch, mosquito bite, pimple.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Purpose of inflammatory response

A

1. Reduce spread of infection by destroying pathogen and prevent entry of any more
2. Remove damaged tissue and cell debris
3. Begin repair of the area (promote healing)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

4 signs of inflammation

A

1. Redness (vasodilation)
2. Swelling (A.K.A oedema) (vasodilation)
3. Heat (warmth, hot) (vasodilation)
4. Pain: increased swelling due to increased blood supply; increased pressure on sensory neurone; or toxins/chemicals around sensory neurone, or damage to nerve endings.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Mast cells

A

(Specialised Leucocytes)
Are cells present in most tissues of the body (CT’s) filled wt granules. They stimulate/coordinate inflammatory responses.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

complement system

A

A series of 20 or more proteins that aid in non-specific + specific immunity. Made by liver cells and macrophages.
present in blood plasma (normally inactive) and activated by pathogens.
When initiated, 1 protein -> activates the next, + so on- complex cascade of events.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

inflammatory response

A

1. Stimulus = tissue damage or local chemical changes (bacteria present). Mast cells activated by complement proteins then release chemicals: histamines and heparin and other proteins into tissue fluid.
2. Histamine diffuses into capillaries causing them to vasodilate and become ‘leaky’ (more permeable/ gaps appear/ allowing larger cells and fluid to pass through). This increases blood flow to the area -> area swells, red and warm.
3. Heparin prevents immediate blood clotting in area around injury - but a clot of fluid does form (slows down m-o, decreases spread.)
4. Phagocytes (1st cells neutrophil + later monocytes) attracted to area by complimentary proteins + histamine chemicals. Phagocytosis occurs (engulf and digest dead cells & bacteria).
5. Pain receptors stimulated in inflamed area - to warn you damage occurred.
6. Pus (yellow liquid) forms = dead phagocytes (neutrophils) + dead microbes + cell debris + tissue fluid.
7. Mitosis produces new cells to repair damaged tissue. (Platelets form fibrin clot).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Fever

A

fever is where the body’s core temperature is reset at a higher temperature - due to an infection
An elevation of body temp above the normal level of 37.C
Non-specific, internal defence mechanism.
Actual body temperature and thermostatic set points are different during a fever. Must be brought in line (or will disrupt normal biochemical processes in the body)
when body temp lower then set point -> heating mechanisms activated
When body temp higher then set point -> cooling mechanisms activated.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

Main causes of fever

A

1. Entry of pathogen/infections produces chemicals/pyrogens which triggers fever.
2. Body releases its own chemicals - pyrogens - that produce a fever.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

steps of fever

A

1. During an infection (eg.cold, flu) activated macrophages (WBCs) inject pathogens + release chemicals- a pyrogen.
2. These pyrogens move to the hypothalamus (important role in ‘thermoregulation’) which resets the body’s thermostat… from the optimal core body to a higher set point. (No thermoreceptors involved).
3. Fever onset: one has the chills, feeds ‘cold’, clammy to touch, as their body temp is now well below the new set point.
4. Chill phase: shivering (increased metabolic heat) and bv vasoconstriction (reduce heat loss) results in increases metabolic rate - causing body temp to rise. (Increased heart rate also to deliver WBCs to infection sites).
5. Crisis point: when the fever ‘breaks’ - where pathogens now destroyed/ infection subsides, the thermostat reduces down to normal 36.8.C. (heat losing mechanisms activated) so the person now feels hot - sweating and skin vasodilation to increase heat loss. Person’s skin to warm and has hot flushes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

pyrogen

A

A fever producing substance (or pathogen releases toxins)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

benefits of fever

A

1. Inhibit the growth/destroys pathogen
2. Inhibits viral replication - allows chemicals called interferons to operate more quickly.
3. Increased heart rate/blood flow: enables WBCs to reach site of infection faster.
4. Heat speeds the rate of chemical reactions -> promotes healing/ tissue repair.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Interferons

A

are proteins secreted by cells that have been invaded by viruses.
They alert other cells to make antiviral proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Consequences of fever

A

too high fever -> denaturing of proteins.
Convulsions, brain damage, loss of consciousness, coma, death.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

lymphatic system function

A

1. To collect fluid that escapes from the blood capillaries and returns it to circulatory system
2. Important role in body’s internal defence against pathogens - helps immune system
3. Transports dietary fats

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

Lymphatic system components

A

network of bind ended lymph capillaries join to larger lymphatic vessels (have valves).'
Lymph nodes containing lymphoid tissue with macrophages and lymphocytes - filters fluid before returned.
cris-crossed network of fibres in nodes, micro-organisms get trapped, macrophages ingest + destroy by phagocytosis.
Lymph fluid originates from tissue - contains cell debris, foreign particles + pathogenic micro-organisms.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

Lymphatic system organs

A

1. tonsils
2. adenoids
3. spleen
4. thymus
5. Bone marrow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

Infections of the body occur when:

A

1. Lymphocyte number increases
2. Lymph nodes become swollen and painful to touch

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Swollen nodes caused infections such as:

A

cold/flu
Abscessed or impacted tooth
gum disease, mouth sores
Skin infection
STDs

28
Q

Immune response

A

the immune response is the homeostatic mechanism, with the body needing to destroy a pathogenic invasion and return internal environment back to normal.
Immune system is made up of specialised cells and proteins that circulate in the blood, Extracellular fluid, lymphoid tissue and in some body organs.

29
Q

2 types of immune response

A

1. Antibody mediated (humoral) response
2. Cell-mediated response
These are immune responses that combat one specific type of pathogen/antigen
specific immunity is acquired through natural infection or immunisation.

30
Q

2 types of Lymphocytes

A

B-lymphocytes (B-cell)
T-lymphocytes (T-cell)

31
Q

Lymphocytes

A

all lymphocytes arrive in red bone marrow - 1/2 migrate to the thymus and mature there (now called T-cell) other 1/2 remain in the red bone marrow and mature there (now called B-cells).
Both end up in lymphoid tissue: lymph nodes, spleen, thymus gland, tonsils
B-cells ‘educated’ or mature in bone marrow
T-cells are ‘educated’ or mature in the thymus

32
Q

Thymus

A

a gland located in the upper chest just above heart, behind sternum.
Largest, active infants and children, around puberty it atrophies (gets smaller) yet maintains its function.
Secretes hormones called thymosines - which promotes the maturation of T-cells
they are educated regarding the body’s own individual self or non-foreign antigens versus non-self or foreign antigens.

33
Q

Antigen

A

Any substance capable of causing a specific immune response
eg. Bacteria, blood transfusion, cancer cells, translated organ.
A non-self antigen (foreign) and is attacked. Self-antigens present on all cells (especially RBC)

34
Q

Antibody

A

A Y-shaped or immunoglobulin (Ig) protein made by plasma cells
5 classes: IgA, IgD, IgE, IgG, IgM
Specific active sites on antibody + active site of antigen - antigen - antibody complex lock and key principle
each antibody can bind 2-6 antigen molecules = Y shaped.

35
Q

Antigen-presenting cells (APC)

A

are phagocytotic cells that digest pathogens and present the antigen to lymphocytes eg. Macrophages and dendritic cells (branch-like extensions) + undifferentiated B-cells.

36
Q

APC role

A

1. Detect presence of a non-self antigen
2. Engulf the pathogen
3. Digest the pathogen (lysosomes) + produces small fragments that move to the surface of the cell
4. present the antigen to lymphocytes

37
Q

B-cells

A

Humoral immunity (body fluid)
antibody mediated immunity
Chemical-based system
Produce antibody (Ig) (attack is indirect on pathogen)
Lymphocytes educated in bone marrow
effective against extracellular bacteria, toxins, some viruses - before they enter the body cells. Also RBCs of diff. Blood group.

38
Q

T-cells

A

Cellular immunity
Cell-mediated immunity
cell-based system
Produce killer T-cells (attack is direct)
Lymphocytes educated in thymus
Effective against intracellular viruses, cancer cells (some bacteria) transplanted foreign tissue/organs, AIDS, fungi and parasites

39
Q

Antibody mediated immunity and cell-mediated immunity

A

These 2 pathways work separately and together to protect us from disease.
however, the events that immediately follow the antigen/pathogen entering the body are common both ‘parts’ of the immune response.

40
Q

How antibodies work (6 ways)

A

1. Inactivate foreign enzymes or toxins by combining with them or inhibiting their reaction wt other cells or compounds
2. Binding to surface or virus and preventing them from entering body cell.
3. Coat bacteria so more easily consumed by phagocytes
4. Agglutination (clumping together) of antigens (or foreign cells)
5. Dissolve organisms
6. Reacting with soluble antigens to make them insoluble enhances phagocytosis.

41
Q

Antibiotics

A

drugs that are used to fight infections of micro-organisms
Can’t be used to treat viral infections
each antibiotic is effective for only certain types of bacterial infections

42
Q

2 types of antibiotics

A

1. Bactericidal antibiotics
2. Bacteriostatic antibodies

43
Q

Bactericidal antibiotics

A

Kill bacteria by changing the structure of the cell wall or cell membrane, or by disrupting the action of essential enzymes
eg. Cephalosporin

44
Q

bacteriostatic antibodies

A

Stop bacteria from reproducing, usually by disrupting protein synthesis.
Eg. Streptomycin, erythromycin, neomycin, tetracycline, vancomycin

45
Q

types of bacteria affected

A

Broad-spectrum antibiotics
narrow-spectrum antibiotics: are only effective against specific types of bacteria.

46
Q

Multiple drug resistance

A

resistance of some strains of bacteria to most of the available antibiotics

47
Q

Total drug resistance

A

the resistance of some strains of bacteria to all bacterias

48
Q

Antivirals

A

used specifically for treating viral infections
Inhibit the development of the virus

49
Q

body’s defences

A

1. Non-specific - work against all pathogens, body’s first line of defence

50
Q

specific defences

A

Directed at a particular pathogen

51
Q

external defences

A

skin
Sebum
sweat
Mucous
hairs
Cilia
acids
Lysosome
cerum
Movement of fluid

52
Q

protective responses

A

Involuntary, automatic response
protects from: injury and infection

53
Q

Reflexes to protect against infection

A

1. Sneezing - forceful expulsion of air from the lungs carries mucous, foreign particles and irritating gases out through nose and mouth.
2. Coughing - air drives mucous and foreign matter up the trachea towards the throat and mouth
3. Vomiting - contraction of abdomen and intercostal muscles, not the stomach, expels the stomach contents
4. Diarrhoea - irritation causes increased contractions of the muscles of the wall of the intestines so that the irritant is removed as quickly as possible. Material doesn’t stay in large intestine long enough for water to be reabsorbed, so fences are very watery.

54
Q

Internal non-specific defences

A

if pathogens get past our external defences, there are internal non-specific defences that work to eliminate them

55
Q

Types of phagocytic cells

A

1. Monocytes and macrophages
2. Neutrophils
3. Dendritic cells

56
Q

Monocytes and macrophages

A

when a tissue becomes infected or inflamed
Monocytes leave bloodstream and enter the tissue
monocytes differentiate into macrophages: large phagocytic cells
Some macrophages go around the tissue looking for and destroying pathogens, others are fixed in one place and only deal with pathogens that come to them.
macrophages important in removing microbes and dying cells through phagocytosis

57
Q

Neutrophils

A

During infection, neutrophils are first cells to move into the tissue to destroy the pathogen by phagocytosis.
Die a few days after, dead cells make up most of pus that forms from infection.

58
Q

dendritic cells

A

Characterised by projections from the cytoplasm.
different to macrophages and neutrophils as their function goes beyond just phagocytosis
Ability to detect, engulf and process foreign particles
use information about ingested particles to assist with specific immunity.

59
Q

3 types of t-cells

A

1. Killer T-cells
2. Helper T-cells
3. Suppressor T-cells

60
Q

Passive immunity

A

when someone receives antibodies produced by someone else, meaning that individual’s body plays no part in the production of antibodies

61
Q

Active immunity

A

results when body is exposed to a foreign antigen and manufactures antibodies in response to that antigen
Lasts long due to presence of memory cells.

62
Q

vaccines

A

1. Live attenuated vaccine
2. Inactivated vaccine
3. Toxoid vaccine
4. Sub-unit vaccine

63
Q

Live-attenuated vaccine

A

living attenuated micro-organisms, micro-organisms of decreased virulence, micro-organism wt reduced ability to produce disease symptoms.
Person manufactures antibodies without contracting the disease

64
Q

inactivated vaccine

A

Contain dead micro-organisms
immunity shorter lasting than live attenuated micro-organisms

65
Q

Toxoid vaccines

A

cases where bacteria produce their effects in humans by liberating toxins
Toxins produced by bacteria can be inactivated so doesn’t make person sick
toxoid - toxin from pathogenic organism that is altered so that it is no longer toxic

66
Q

Sub-unit vaccines

A

fragment of the organism is used to provoke immune response
Used for human papilloma virus and hepatitis B

67
Q

vaccine delivery

A

injection
Oral - in lumps of sugar or syrup