8.1 Adaptive immunity Flashcards

1
Q

Describe adaptive immunity.

A
  • Specific
  • Slow response
  • Requires exposure to pathogen
  • Memory, response improves upon subsequent exposure
  • Includes lymphocytes, antigen-recognition molecules (B and T cell receptors), antibodies
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2
Q

What are the genetic differences between adaptive and innate immunity?

A
  • Receptors involved in innate immunity are germline encoded
  • Receptors in adaptive immunity are somatically arranged receptors
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3
Q

Give 6 features of adaptive immunity.

A
  • Specificity
  • Diversity
  • Tolerance: chance of autoimmune attack
  • Circulation: lymphocytes specific to a pathogen will travel through the circulation
  • Division of labour: not all lymphocytes work equal amounts, they each have their own role
  • Memory
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4
Q

The immune system protects against 4 classes of pathogens, what are these?

A
  • Extracellular bacteria, parasites, fungi
  • Intracellular bacteria, parasites
  • Viruses (intracellular)
  • Parastitic worms (extracellular)
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5
Q

What does colonal selection refer to?

A

The process by which the body produces B and T cells to respond to infections.
Describes how diversity, specificity and tolerance are generated.

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6
Q

What form is the T-cell receptor found in?

A

Found in membrane bound form.

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7
Q

What form is the B-cell receptor found in?

A

Found in membrane bound form or in a secreted form.

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8
Q

What are the 2 domains of a T- and B-cell receptor?

A

They each have a variable domain and constant domain.

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9
Q

Describe the variable domain of T- and B- cell receptors.

A
  • The variable domain/region is involved in recognising the antigen
  • Within the variable domain there are hypervariable regions involved in recognising pathofens
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10
Q

What are the 3 mechanisms by which antibodies counter extracellular infection?

A
  • Neutralisation of bacterial toxins
  • Opsonisation of bacteria found in the extracellular space
  • Complement activation of bacteria found in plasma
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11
Q

What is an epitope?

A

Epitope = the region of an anitgen recognised by a B/T cell

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12
Q

How do T cell epitopes differ from B cells?

A

T cell epitopes can be internal and external.
B cells only have cell surface epitopes.

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13
Q

What does MHC stand for?

A

Major histocompatibility complex

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14
Q

What are the 2 classes of MHC molecules?

A
  • MHC class I: recognised by CD8 positive cytotoxic T cells
  • MHC class II: recognised by CD4 positive T helper cells
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15
Q

Describe MHC class I receptors in the process of destroying viruses.

A
  • Virus enters cell and expresses antigens in the cytosol of the cell
  • Viral proteins broken down into peptides
  • Peptides pass into the ER, MHC class I receptors bind to peptides
  • Complex of MHC and viral peptide move to cell surface
  • Cytotoxic T cell (CD8 positive) recognises complex and kills infected cell
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16
Q

Describe MHC class II receptors in the process of destroying extracellular bacteria, parasites and fungi in macrophages.

A
  • Macrophage engulfs and degrades bacterium, producing peptides
  • Bacterial peptides bound by MHC class II in vesicles
  • Bound peptides are transported by MHC class II to the cell surface
  • T-helper cell (CD4 positive) recognises complex and activates macrophage
17
Q

Describe MHC class II receptors in the process of destroying extracellular bacteria, parasites and fungi in B cells.

A
  • Cell-surface immunoglobulin of B cell binds bacteria and engulfs into cell
  • Degrades bacteria to produce bacterial peptides
  • Peptides bind to MHC class II proteins in endocytic vesicles and transported to cell surface
  • T-helper cell recognises complex and activates the B cell to produce antibodies
18
Q

How is BCR and TCR diversity generated?

A

B and T cell receptor diversity.
2 mechanisms:

  • Combinatorial diversity: different combinations of varibale gene segments
  • Junctional diversity: loss or gain of nucleotides at junctions
19
Q

What is the risk that comes with the way BCR and TCR diversity is generated?

A

Because different gene segments are brought together in a random fashion, it is possible for us to produce antibodies against our own antigens- risk of autoimmune disease.

20
Q

Where do antigen specific T cells encounter antigen presenting cells?

A

In the lymph nodes and secondary lymphoid tissue (spleen).

21
Q

Describe the dendritic cell.

A
  • Professional antigen presenting cell
  • Many dendrites making them efficient at phagocytosis and pinocytosis
  • Have large numbers of toll like receptors (activation of these enhances processing of pathogen-derived antigens)
22
Q

Describe the action of dendritic cells when they encounter a pathogen.

A
  • Immature dendritic cells encounter pathogens and are activated by PAMPs
  • TLR signaling induces the CCR7 receptor and enhances processing of pathogen-derived antigens
  • CCR7 directs migration into lymphoid tissues and augments expression of co-stimulatory molecules and MHC molecules
23
Q

What are the 3 routes of antigen processing and presentation by dendritic cells?

A
24
Q

What is a key function of mature dendritic cells?

A

Mature dendritic cells are extremely efficient at stimulating naive T cells.
Known as priming.

25
Q

How do lymphocytes and lymph return to blood from the site of infection?

A

Via the thoracic duct

26
Q

Summarise T cells and their functions.

A

5 types:
- CD8+ (cytotoxic) = kill virus infected cells
- CD4TH1 = activate infected macrophages, provide help to B cells for antibody production
- CD4TH2 = provide help to B cells for antibody production, especially switching to IgE
- CD4TH17 = enhance neutrophil response
- CD4 regulatory T cells = suppress T-cell responses

27
Q

Summarise B cells and their functions.

A
  • Produce antibodies
  • IgM, IgD, IgG, IgE, IgA
  • The constant region of the heavy chain is the one that changes between isotypes
  • IgM is the first antibody produces by B cells
  • IgM is good for activating complement but offers poor tissue penetration, isotype will change to a different type of immunoglobulin depending on what traits are desired
28
Q

Which 2 antibodies are most prevalent in the oral cavity?

A
  • IgA present in saliva
  • IgG in gingival crevicular fluid
29
Q

How does antibody quality change during the course of an adaptive immune response?

A
  • IgM is the first antibody produced
  • Somatic hypermutation takes place (point mutations introduced into variable segments to increase affinity of antibody for antigen)
  • Class switching occurs (switching antibody isotype) to IgG which means IgG can act as an opsonin and enhance phagocytosis
30
Q

Each antibody has different specialised functions, what are some of these?

A
31
Q

How does vaccination work?

A
  • Vaccines expose an individual to an attenuated form of a virus, or a safe component of a pathogen
  • Body produces T and B memory cells which survive in lymph nodes or peripheral tissues