11. Immunity Flashcards

1
Q

Explain how macrophages function to protect the lungs from becoming infected. [4m]

A
  • macrophages recognise non-self antigens on pathogens
  • receptor on macrophage binds to antigen on pathogen
    or pathogen adheres to CSM
  • infolding of macrophage CSM around / engulf pathogen
  • vesicle forms
  • lysosomes that contain hydrolytic enzymes destroy pathogen
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Explain why polysaccharides would not be suitable for making antibody molecules. [2m]

A
  • polysaccharides are made from a small number of different sugars
  • unlike proteins which are made from 20 amino acids
  • polysaccharides would not give the huge no. of different molecular shapes in the variable region of antibodies as is achieved with proteins
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Suggest why the results for a single sample of blood taken from a patient on admission to hospital should be interpreted with care. [3m]

A
  • the patient may never have had such a blood test before
  • there is no way to know if the no. of blood cells have changed as a result of infection
  • wide ranges of results are normal
  • there are a variety of causes for high or low numbers of blood cells
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Explain why myasthenia gravis (MG) is known as an autoimmune disease. [3m]

A
  • failure to distinguish between self and non-self
  • specific B-lymphocytes are not destroyed during development
  • antibodies are produced against ACh receptor on muscle cells
  • antibodies bind to receptor
  • thus acetylcholine cannot bind to receptor
  • nerve impulses are not transmitted across neuromuscular junction
  • causing muscle fatigue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Suggest why MG is a long-term condition. [2m]

A
  • immune response occurs all the time
  • defective B-lymphocytes still being produced
  • plasma cells continue to release antibodies against receptors
  • memory cells present
  • no cure
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

A monoclonal antibody is labelled with the radioactive isotope indium-111, which emits low-energy gamma rays that can pass through soft tissues of the body. The half life of indium-111 is 2.8 days

Suggest why indium-111 is a suitable radioactive label for this diagnostic antibody. [3m]

A
  • emits gamma-rays, which pass though soft tissues and so can be diagnosed from outside the body
  • weak gamma-rays, reducing chance of mutation
  • short half-life, so no continuing source of gamma-rays
  • indium has no biological role
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Monoclonal antibody

A
  • identical antibodies produced by cloning

- variable regions/antigen-binding sites are all identical; antibodies are specific to 1 antigen

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

Explain how vaccination can control infectious diseases. [3m]

A
  • vaccination gives active IMMUNITY
  • clonal selection/expansion of specific B-lymphocytes occurs, involving formation of antibodies and memory cells
  • presence of antigen gives faster, secondary immune response
  • effect of vaccination is long-lived as memory cells remain in circulation for long time
  • herd effect produced when >90% people vaccinated, so non-vaccinated people are protected
  • stop transmission cycle
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Explain why countries that have established vaccination programmes still have cases of measles. [2m]

A
  • measles introduced by people who caught the disease when abroad
  • herd immunity needs to be >90%
  • some people in these countries have not vaccinated
  • some people do not respond to vaccine (weak immune system/malnutrition)
  • some people do not receive boosters
  • vaccine is not thermostable
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Some strains of V. cholerae are antibiotic resistant.

Explain why medical practitioners prefer to treat cholera with a single dose of antibiotic, rather than a multiple dose of the same antibiotic. [2m]

A
  1. single dose is easier to ensure patient has taken complete dose; course may not be completed for multiple dose
  2. if all bac. are susceptible and treatment completed, all bac. killed by single dose; if multiple dose given, treatment may not be completed so some susceptible bac. survive
  3. thus multiple dose increases chance of mutation
  4. if resistance already present, single stronger dose has greater chance of killing resistant bac.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Explain why the concentration of antibody (eventually) falls. [3m]

A
  • no more antigen
  • no more antibodies produced
  • plasma cells are short-lived
  • antibodies eventually broken down in liver
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Outline the use of monoclonal antibodies in the treatment of disease. [2m]

A
  • specific treatment
  • bind to antigens on cell surface of diseased cells
  • kill the cell by stimulating immune system
  • attach radioactive substances/drug to kill diseased cells
  • treat infectious diseases / bind to antigens on pathogens
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

6 advantages of using monoclonal antibodies in diagnosis of disease

A
  1. monoclonal antibodies used all have the same specificity
  2. detect only one antigen
  3. can distinguish between different pathogens
  4. can be labelled/tagged, eg. with fluorescent label
  5. can detect location of tissue expressing antigens / cancer cells / blood clots
  6. faster diagnosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Immune response

A

The reaction of the body to the presence of a foreign antigen

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

Describe how mitosis is involved in an immune response. [3m]

A
  • occurs in both primary & secondary immune response
  • SPECIFIC B- and T-cells divide by mitosis
  • clonal expansion producing clones
  • mitosis in memory cells for rapid secondary response
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

4 advantages and 5 disadvantages of artificial passive immunity

A

Advantages

  1. antibodies are provided to people immediately
  2. antibodies immediately neutralise toxins / prevent viruses entering cells
  3. prevents disease in the individual
  4. prevents spread of pathogen through the population

Disadvantages

  1. short-term immunity
  2. no memory cells produced
  3. can have infections of SAME pathogen again
  4. allergic reaction / immune response to the (non-human) antibodies given
  5. high cost of production of antibodies
17
Q

Very few helper T-lymphocytes respond to the presence of APCs by binding.
Suggest why this is so. [2m]

A
  • only a few with correct specificity
  • different T-lymphocytes are specific to different ANTIGENS
  • T cell receptor is complementary in shape to antigen