adaptive immunity (basics) (W11) Flashcards

1
Q

name for lymphocyte is its never been activated

A

naïve lymphocyte

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2
Q

what occurs to a lymphocyte after it binds to their specific antigen

A

activated and differentiate into effector cells - either T cells or effector B cells

also differentiate into memory T/B cells

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3
Q

B cells function?

A

produce antibodies

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4
Q

what occurs to B cells once activated

A

become plasma cells (aka effector B cells)

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5
Q

variable region on antibody?

A

antigen binding site, varies between antibodies

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6
Q

T cells that kill virally infected cells?

A

CD8+ Cytotoxic T lymphocyte (CTL)

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7
Q

T cells which organise immune responses by producing different cytokines

A

CD4+ T helper cell (Th cell)

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8
Q

first thing that occurs after a T/B cell binds to its specific antigen

A

proliferates
some daughter cells go on to become memory cells

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9
Q

generation of BcR/TcR diversity - random

A

variable regions encoded by variable, diversity and joining gene segments (V,D,J).
gene must be rearranged (somatic recombination, DNA chopped out).
many different variable regions on one B cell receptor.
random mix of V D and J.

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10
Q

name for specific binding site of an antigen

A

epitope

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11
Q

2 classes of MHC and what they bind to

A

CD8+ CTLs bind antigen on class 1 MHC
CD4+ T helper cells bind antigen on class 2 MHC

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12
Q

where is class 1 MHC present? why?

A

on the surface of all nucleated cells
presents endogenous proteins of that cell on the cell surface

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13
Q

where is class 2 MHC present? which of these are the most important?

A

specialised antigen presenting cells (APC)
most important of which are dendritic cells

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14
Q

function of class 2 MHC?

A

present exogenous antigens

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15
Q

structure of class 1 MHC?

A

alpha chain (made of 3 domains) bound to beta-2 macroglobulin
alpha 1 and 2 domains make up peptide-binding cleft

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16
Q

structure of class 2 MHC?

A

alpha and beta chain
(2 alpha domains, 2 beta domains)
alpha 1 and beta 1 domain make up peptide-binding cleft

17
Q

why is diversity in MHC required

A

increases the diversity of antigens presented to T cells

18
Q

what part of MHC do peptides bind to?

A

anchor pockets (vis anchor amino acids)

19
Q

what do anchor pockets react with?

A

only a limited range of biochemically similar ‘anchor’ amino acids on peptides

20
Q

strategies to overcome the limited range of anchor pocket reactions

A

polygeny - multiple independent genes for each MHC type
co-expression - alleles inherited from mother and father
polymorphisms - multiple variants of each gene within the human population

21
Q

why is polymorphism important in regards to viruses

A

viruses evolve to edit out certain amino acid sequences from there viral genome, polymorphism stops this by presenting as many different peptides as possible

22
Q

MHC in transplant rejection?

A

very rare for 2 unrelated individuals to express the same combination of MHC variants - transplant seen as non self

23
Q

prevention of unnecessary and harmful responses to self and environmental antigents?

A

immunological tolerance

24
Q

2 types of immunological tolerance

A

central and peripheral tolerance

25
Q

what is central tolerance

A

deletion of self reactive T cells in thymus and B cells in bone marrow

26
Q

what is peripheral tolerance

A

activation of lymphocytes requires recognition of danger. recognition of antigen in the absence of danger causes lymphocytes to become anergic or die

27
Q

central tolerance in the thymus?

A

eliminates harmful and rejects the useless T cells
positive and negative selection

28
Q

what makes a T cell useless

A

can’t bind MHC

29
Q

what happens when strong signalling occurs between MHC presenting self-peptide and T cell

A

signal causes cell death - this is negative selection (in the thymus)

30
Q

what happens when strong signalling occurs between MHC presenting self-peptide and T cell

A

signal causes cell death - this is negative selection (in the thymus)