L41. Adaptive Immunity Flashcards

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1
Q

Name the 2 types of adaptive immune response.

A

Cell-mediated response

antibody (humoral) response

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2
Q

Cell mediated immunity: which cells is it driven by?

A

T cells

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3
Q

Cell mediated immunity : what does it involve the activation of?

A

macrophages
natural killer cells
cytotoxic T-lymphocytes

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4
Q

Humoral immunity : which cells drive it? Why?

A

B-cells produce antibodies

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5
Q

How does immunological memory occur?

A

When a pathogen is remembered by a signature T cell and/or B cell receptor

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6
Q

What is the time frame for adaptive immunity?

A

4-7 days from the start of infection

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7
Q

Describe the 2 stages following “recognition by naïve B and T cells”.

A
  1. Clonal expansion and differentiation

3. Removal of infectious agent

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8
Q

Name 3 adaptive immunity receptors

A
  1. T cell receptors
  2. B cell receptors
  3. MHC proteins
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9
Q

What do T cells do?

A

Give rise to cellular immunity.
Can respond to many antigens, called “T cell repertoire”.
“Thymic education” means they only respond to foreign pathogens

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10
Q

What is the role of CD4+ cells?

A

T helper cells which help support other immune cells to fight threats

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11
Q

What are CD8+ cells?

A

Cytotoxic T cells which destroy infected self cells

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12
Q

What do T-regs do?

A

Regulate or suppress other immune cells

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13
Q

How do all cells start?

A

As naïve cells and have protein specific receptors

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14
Q

Name the co-receptors of the following and what they each bind to.
CD8
CD4

A

CD8 has a co-receptor that binds to MHC1

CD4 has a co-receptor that binds to MHC2

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15
Q

What is CD3?

A

A co-receptor involved in CD4 and CD8 T-cell activation

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16
Q

What are most T cell receptors made of?

A

alpha and beta chains

17
Q

Name the 2 regions which make up the T cell receptor.

A

Constant region

Variable region

18
Q

Which genes make up the variable region, and which chains are they found on?

A

V (variable) (alpha and beta)
J (joining) (alpha and beta)
D (diversity) (beta only) (closes to B in alphabet)

19
Q

How are genes re-arranged, and by which enzymes?

A

Somatic recombination by RAG enzymes

20
Q

Name the 2 types of T cell selection after the thymus interaction.

A

Positive selection

Negative selection

21
Q

What happens to positively and negatively selected CD4/CD8 cells?

A

Leave the thymus and regulate in the blood/lymphatics.

22
Q

*Even although cells which leave the thymus (to regulate in the blood) are educated, what cell type are they still classed as?

A

“Naïve T cells”

23
Q

What do immature dentritic cells do?

A

Take up the antigen to be processed in the epidermis. They migrate to the lymph nodes and mature on the way.

24
Q

What does “priming” refer to?

A

The 3 signals required for activation and fate determination of T cells.

25
Q

Name the middle step.

  1. Activation of T cell by T cell receptor and MHC2. (this is known as anergy if step 2 is absent)
  2. ___________________
  3. differentiation into subsets of effector T cells (using cytokines)
A
  1. Activation of T cell by T cell receptor and MHC2. (this is known as anergy if step 2 is absent)
  2. Survival and clonal expansion of T cells using CD28
  3. differentiation into subsets of effector T cells (using cytokines)
26
Q

Name the 5 CD4 cell subsets.

A
Th1
Th2
Th17
Tfh
Treg
27
Q

Give the role and source of Th1

A

supporting macrophage function

interferon y

28
Q

Give the role and source of Th2

A

supporting humoral responses and allergic reactions

interleukin 4,5 and 6

29
Q

Give the role of Th17

A

Supports innate immune responses

30
Q

Give the role of Tfh

A

T follicular helper cells work with b cells for antibody production

31
Q

Give the role of Tregs

A

Immune suppression, inhibit T cell and dendritic cell activation.

32
Q

What activates CD8 cells?

A

T cell receptor and MHC1 interaction

33
Q

What does CD8 activation result in?

A

Induces host cell apoptosis

produces enzymes

34
Q

What is the activation of T cells called? What does it result in?

A

Activation is called priming.

Results in the generation of memory T cells