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
what is central tolerance
deletion of self reactive T cells in thymus and B cells in bone marrow
26
what is peripheral tolerance
activation of lymphocytes requires recognition of danger. recognition of antigen in the absence of danger causes lymphocytes to become anergic or die
27
central tolerance in the thymus?
eliminates harmful and rejects the useless T cells positive and negative selection
28
what makes a T cell useless
can't bind MHC
29
what happens when strong signalling occurs between MHC presenting self-peptide and T cell
signal causes cell death - this is negative selection (in the thymus)
30
what happens when strong signalling occurs between MHC presenting self-peptide and T cell
signal causes cell death - this is negative selection (in the thymus)