Disease and immunity Flashcards

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1
Q

What are the four main types of pathogen?

A

Bacteria
Viruses
Fungi
Protoctista

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2
Q

What is active immunity?

A

Something that stimulates the production of antibodies and memory cells. Long-lasting.

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3
Q

What is passive immunity?

A

Something that introduces antibodies from a outside source, but does not stimulate memory cell production. Short lived.

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4
Q

What do natural and artificial mean in terms of active immunity?

A
Natural = From a body's own response
Artificial = Stimulating a response by introducing a dead or altered pathogen
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5
Q

What do vaccines involve?

A

Introducing a modified antigen, killed pathogen or non-virulent pathogen to a person’s immune system

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6
Q

What must good vaccines be?

A

Good vaccines must be:
· thoroughly tested to ensure few, if any, side effects
· economical to vaccinate a whole population or age group (routine)
· easy to produce, store, transport and administer

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7
Q

What are some direct forms of transmission?

A

Physical contact
Droplet spread
Spores

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8
Q

What are some indirect forms of transmission?

A

Airborne particles
Contaminated objects
Vectors
Contaminated food and water

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9
Q

What factors can contribute to the spread of disease?

A

· hot, humid climate
· overcrowding and homelessness
· poor ventilation
· malnourishment and polluted water and food
· poor health and access to health care
· lack of hygiene and poor hygienic services

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10
Q

Where can we get medicines from?

A

Medicines are from many microorganisms and plants; These can be antigens they produce, or even toxins.

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11
Q

What key features do antibodies have?

A

· two binding sites
· variable regions that are complementary to different antigens
· constant region
· four polypeptide chains called immunoglobins

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12
Q

What defences do plants have against invading pathogens?

A

Structural Chemical

Permanent Bark, waxy cuticle Not applicable
tough cell walls

Synthesised Callose deposition Cell suicide, toxic
substances,
pathogen-degrading
enzymes

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13
Q

Why must you be careful with antibiotics, and how can you minimise this risk?

A

There may be some resistant bacteria which will then reproduce, forming an antibiotic resistant population. You can minimise this by rotating antibiotics often and only using them if completely necessary.

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14
Q

What makes up the first line of defence against pathogens in animals?

A
· keratinised dead skin cells 
· blood clotting and wound repair 
· mucous membranes and cilia 
· inflammation 
· expulsive reflexes (diarrhoea and vomit)
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15
Q

What do T helper cells do?

A

Recognise antigens displayed on phagocytes and stimulate specific T killer cells and B cells (clonal selection) to divide by mitosis (clonal expansion)

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16
Q

What do T killer cells do?

A

These are cytotoxic – they kill infected cells by creating a hole in their cell membrane

17
Q

What do T memory cells do?

A

Remain in the blood to provide a rapid response to reinfection

18
Q

What do T regulator cells do?

A

Suppresses self-recognising immune cells

19
Q

What do B plasma cells do?

A

Release monoclonal antibodies which form an antigen–antibody complex, causing agglutination and attracting phagocytes to destroy the immobilised pathogens

20
Q

What do B memory cells do?

A

Remain in the blood to provide a rapid response to reinfection

21
Q

What do phagocytes produce and what do each of them do?

A

cytokines (regulate the immune response)
interleukines (trigger replication of other white blood cells)
opsonins (bind to a pathogen and signal for phagocytosis)
anti-toxins (bind and disable toxins)

22
Q

What are the stages of phagocytosis?

A
  1. Pathogens produce chemicals that attract phagocytes
    1. Phagocytes recognise non-human proteins on the pathogen. This is general, non-self-reaction
    2. The phagocyte engulfs the pathogen and encloses it in a vacuole called a phagosome
    3. The phagosome combines with a lysosome to form a phagolysosome
    4. Enzymes from the lysosome digest and destroy the pathogen.
23
Q

What are the three modes of action of antibodies?

A
  1. Opsonins - Coat pathogen binding sites so unable to infect cells. Phagocytes recognise the antibodies and
    engulf the pathogen.
  2. Agglutination - Large antibodies bind many pathogens so clump is too large to enter cells and is more likely to be phagocytosed.
  3. Anti-toxin precipitation - Soluble toxins released by bacteria are precipitated out of solution so can be phagocytosed more easily.
24
Q

Where does the cell-mediated response occur?

A

In the tissues

25
Q

Where does the humoral response occur?

A

In the bodily fluids / surfaces

26
Q

What are the stages of cell mediated response?

A
  1. Phagocytes present antigens they have found
  2. T helper cells fit the specific antigen. This causes them to produce interleukins which stimulate more T cells to divide by mitosis.
  3. These cells can do any of the T cell functions.
27
Q

What are the stages of humoral response?

A
  1. Activated T helper cells bind to the B cell APCs (antigen presenting cells). This cell then repeatedly divides.
  2. Interleukins produced by activated T cells cause the B cells to activate.
  3. These B cells divide by mitosis to form Plasma cells and B memory cells
  4. These B cells produce antigens that combat the pathogen
  5. The B memory cells stay in case of re-invasion