Lec 33 - Ab distribution and function Flashcards

(20 cards)

1
Q

what type of immunity is achieved via vaccines?

A

induced active immunity

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2
Q

what are the 2 types of vaccines? expand

A

component vaccines (RNA, DNA, virus-like particles, protein subunits, viral vectors)
whole vaccines (killed pathogen, live attenuated)

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3
Q

what are the key functions of Abs? general

A

neutralisation (blocks pathogen-host binding, cant exert their effect)

opsonisation (enhance phagocytosis of macrophages, etc)

complement fixation (C1q binding, classical activation)

Ab-dependent mediated cytotoxicity (NK induced)

trigger degranulation via Fc

transport (for all of the above)

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4
Q

what do Fc recepotrs bind to?

A

Fc portion of Abs
each type of Fc receptor can only bind to one class of Ig (binding is class specific, not one fits all)

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5
Q

where are Fc receptors found?

A

on a lot of innate immune cells

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6
Q

what is the role of Fc receptors?

A

mediate many effector Ab functions only if Fc receptor is crosslinked to Fc and Ab is actually bound to Ag (leads to conformational change in Fc)

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7
Q

what are effector functions that result from Fc-Fcr binding?

A

degranulation and histamine release by Mast cells

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8
Q

how are innate immune cells able to be somewhat specific?

A

via specific Fc receptors

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9
Q

what does opsonisation require?

A

Fc receptors on macrophage binding to Fc of Ab on pathogen

aggregation of binding will lead to cross-linking, triggering intracellular signaling leading to effector functions

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10
Q

what are IgG effector functions?

A

enhance phagocytosis by macrophages (opsonisation)

other functions depends on IgG subclass

some effective at complement fixation, other mediating ADCC by NK cells (function = toxic granule release)

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11
Q

what are effector functions of IgE?

A

degranulation of eosinophils/basophils
histamine release by mast cells

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12
Q

can IgE bind to mast cell before Ag is bound to Ab?

A

yes, wont perform effector function though
requires Fc-Fcr crosslinking to lead to histamine release

is not just specific to IgE, is the case for all Ig classes and effector functions

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13
Q

what pathogens can be neutralised?

A

any intracellular pathogen
toxin, virus, bacteria

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14
Q

what Ig isotypes are good for neutralisation?

A

IgA and IgGw

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15
Q

where is IgA found majority of the time?

A

secretions: gut mucus, mammary gland milk, tears, saliva

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16
Q

how does C1q bind to pathogen?

A

directly or via Abs on surface

17
Q

which Ig isotypes can trigger complement cascade? expand

A

IgM and IgG

especially IgM because of pentavalent, creating nice landing pad for C1q

18
Q

what else is IgM good for?

A

forming dense Ab-pathogen complex (since 10 binding sites), allowing efficient engulfing by macrophage

19
Q

how does transport differ between Ig classes? expand

A

go to different parts of the body
IgA = found in mucosal tissues
IgE = near epithelial surfaces
IgM = blood (but not high quantity)
IgG = widely distributed (inc. fetus)