Module 2 - Cell recognition and the immune system Flashcards

1
Q

5 marks

Describe difference between active and passive immunity

A
  1. Active involves memory cells, passive does not;
  2. Active involves production of antibody by plasma cells / memory cells;
  3. Passive involves antibody introduced into body from outside
  4. Active long term, because antibody produced in response to antigen
  5. Passive short term, because antibody (given) is broken down;
  6. Active (can) take time to develop, passive fast acting.
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2
Q

5 marks

When a vaccine is given to a person, it leads to the production of antibodies against a disease-causing organism. Describe how

A
  1. Vaccine contains antigen from pathogen
  2. Macrophage presents antigen on its surface
  3. T cell with complementary receptor protein binds to antigen;
  4. T cell stimulates B cell
  5. (With) complementary antibody on its surface
  6. B cell secretes large amounts of antibody
  7. B cell divides to form clone all secreting / producing same antibody.
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3
Q

How does passive immunity work

A

Passive involves antibody introduced into body from external source
Adding the antibody would cause agglutination and increase efficiency of phagocytosis

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4
Q

State one role of a helper T cell.

A

Stimulating cytotoxic T cells
Stimulating B cells
Stimulating phagocytes;

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5
Q

The human papilloma virus contains a double-stranded DNA genome.
Which components are found in a human papilloma virus? Choose one
* Capsid and attachment protein
* Capsid, attachment protein and reverse transcriptase
* Capsule and attachment protein
* Cell-surface membrane and attachment protein

A

Capsid and attachment protein

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6
Q

2 marks

Explain why viruses are described as acellular and non-living.

A
  1. Accelular= not made up of cells
  2. Non living= no metabolic reactions/ need a host cell to replicate
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7
Q

Give one reason why antibiotics are not effective against viruses.

A

doesnt have a cell wall

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8
Q

Define pathogen

A

Microorganism that causes disease/ an immune response

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9
Q

3 marks

Describe how phagocytosis of a virus leads to presentation of its antigens

A
  1. Phagosome/ vesicle fuses with lysosome
  2. Virus destroyed by lysozymes/ hydrolytic enzymes
  3. Antigen from virus are displayed on the cell membrane
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10
Q

3 marks

Describe how presentation of a virus antigen leads to the secretion of an antibody against this virus antigen

A
  1. T helper cell receptor binds to antigen on the antigen- presenting cell
  2. T helper cell stimulates a specific B cell
  3. B cell divides by mitosis
  4. Forms plasma cells that release antibodies
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11
Q

3 marks

Describe viral replication

A
  1. Attachment proteins attach to receptors
  2. Viral nucleic acid enters cell
  3. Reverse transcriptase converts RNA to DNA
  4. Cell produces viral proteins
  5. Virus assembled and released from cell
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12
Q

1 mark

There is currently no effective vaccine available for HIV. Suggest one reason why.

A
  1. (High rate of) mutation
  2. (High) genetic diversity
  3. HIV in cells could (still) spread infection
  4. HIV (DNA) embeds/inserts itself in host DNA
  5. Lack of funding/money (for research/development)
  6. HIV causes fewer T cells, so immune response (to the vaccine) does not happen
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13
Q

1 mark

Explain how the stain allowed the doctor to count the white blood cells amongst all the red blood cells.

A

White cells have a nucleus that stains but red cells do not

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14
Q

2 marks

In Europe, viruses have infected a large number of frogs of different species. The viruses are closely related and all belong to the Ranavirus group. Previously, the viruses infected only one species of frog. Suggest and explain how the viruses became able to infect other species of frog.

A
  1. Mutation in the genetic material
  2. Altered tertiary structure of the viral attachment protein
  3. Allows attachment protein to bind to receptors of other species
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15
Q

4 marks

Describe how the human immunodeficiency virus (HIV) is replicated once inside helper T cells (TH cells).

A
  1. RNA converted into DNA using reverse transcriptase
  2. DNA inserted into helper T cell nucleus
  3. DNA transcribed into HIV mRNA
  4. HIV mRNA translated into viral proteins for assembly into viral particles
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16
Q

2 marks

No organelles are visible in the cytoplasm of this red blood cell.
Suggest why

A

Cytoplasm of red blood cell filled with haemoglobin.

17
Q

2 marks

What is a monoclonal antibody

A
  1. Antibody with the same tertiary structure
  2. B plasma and memory cells produce antibodies
18
Q

2 marks

Explain why a test line in elisa test is important

A
  1. Prevents false negative results
  2. Shows antibody has moved up strip and hasnt bound to antigen
19
Q

6 marks

Explain the process of the ELISA test

A
  1. Antibodies complementary to antigen and are bound to bottom of the beaker
  2. When patient sample is added, target antigens bind to antibody
  3. Sample is washed to remove unbound antibodies
  4. Secondary antibodies added with enzyme bound
  5. Wash sample to remove unbound antibodies
  6. Substrate is added (colourless) which reacts with enzyme
  7. If target antigen is present, a colour change takes place
20
Q

1 mark

Define antigenic variability

A

Mutations in DNA cause a changes to tertiary structure of antigens. E.g. different Covid variants

21
Q

Explain primary and secondary immune responses

A

Primary response – memory cells made. Secondary response – Memory cells convert to Plasma [increase in Golgi, RER, mitochondria]. Many Antibodies produced. Rapidly.

22
Q

Give examples of active and passive immunity

A

Active – immune response to pathogen or vaccine
Passive – breast milk or injecting antibodies

23
Q

Outline how the ELISA test works in for the ‘test’ line in a Lateral Flow Test

A

‘Capture’, stationary monoclonal antibody binds to antigen. Monoclonal antibody with label [enzyme] binds to antigen. Substrate changes to coloured product in the presence of enzyme.

24
Q

How could you use the immune response of different animals to analysis evolutionary relationships? [The precipitate method]

A

Give Protein antigens from Species A to Host animal – antibodies made.
Test those antibodies with Species B, C, D. The greater amount of precipitate [Antigen/Antibody complexes] – the more similar the Species B,C or D proteins are to Species A – so closer evolutionary relationship.

25
# 4 marks Describe the structure of the human immunodeficiency virus (HIV)
1. Attachment protein 2. RNA 3. Reverse transcritase 4. Protein capsid 5. Lipid envelope
26
# 2 marks What is an antibody
1. A protein specific to antigen 2. Produced by B plasma cells
27
# 2 marks What is an antigen
1. A foreign protein 2. That stimulates an immune response
28
# 4 marks NMO is a disease that leads to damage to nerve cells in the spinal cord. A person with NMO produces anti-AQP4 antibody that attacks only these nerve cells. Explain why the anti-AQP4 antibody only damages these cells.
1. Antibody has a specific tertiary structure 2. Has variable region that only binds to / complementary to one antigen 3. Antigen to this antibody only found on these nerve cells; 4. So, antibody binds to antigen, forming antigen-antibody complex with these nerve cells, causing damage
29
# 8 marks Describe cellular response | BHA version
1. APC- phagocyte, cancer cell, invaded host cell 2. T helper cell receptors bind to specific and complementary APC presented antigens 3. Cytokines released and stimulates T cells 4. Triggers mitosis and differentiation of T cells (clonal selection) 5. T cells differentiate to cytotoxic T cells and T helper cells 6. Cytotoxic cells release perforin 7. Perforin destroys infected cells 8. Only suitable when pathogens are inside host cells
30
# 10 marks Describe humarol response | BHA version
1. APC- phagocyte, cancer cell, invaded host cell 2. T helper cell receptors bind to specific and complementary APC presented antigens 3. Cytokines released and stimulates B cells 4. Triggers mitosis and differentiation of B cells (clonal selection) 5. B cells differentiate to B plasma cells and B memory cells 6. B plasma cells produce and secrete monoclonal antibodies 7. Antibodies bind to pathogen antigens- form antigen- antibody complex 8. Agglutination 9. Increased efficiency of phagocytosis 10. This is primary response. Memory cells produce secondary response (higher conc of antibodies produced and produced more rapidly- quicker response)
31
# 5 marks Vaccines protect people against disease. Explain how
1. Vaccines contain weakened or inactive forms pathogens/ antigens 2. Memory cells made 3. On second exposure memory cells produce antibodies & recognise pathogens 3. Idea of memory cells responding 4. Rapidly produce antibodies / produces more antibodies 5. Antibodies destroy pathogens