Effector Responses: Humoral and Cell-mediated Immunity Flashcards

1
Q

Neutralization

A

protects against viral or bacteria infection or the damaging effects of toxins

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2
Q

Agglutination

A

enhances neutralization and more efficient clearance of pathogens from the body

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3
Q

Opsonization

A

promotes and or enhances the engulfment of antigens by phagocytosis

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4
Q

Complement Activation

A

result in the generation of the membrane attack complex (MAC), creating pores in pathogen membranes and killing the microbe

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5
Q

Antibody-Dependent Cell-mediated Cytotoxicity (ADCC)

A

activates the killing activity of several types of cytotoxic cells, e.g. NK cells

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6
Q

Antibody-Dependent Degranulation and Mediator Release

A

triggers mediator release from granulocytes

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7
Q

What determines an antibody class

A

constant region determines class, class determines function

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8
Q

How an antibody contributes to clearing infection depends on

A

its class (heavy-chain isotope)

  • controls some of its effector function
  • determines which receptor can bind
  • determines which cells an antibody can activate
  • determines which locations in the body it can gain access
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9
Q

IgM

A
  • First Ab produced in a primary immune response
  • Tends to have lower affinity, high avidity
  • Pentavalent (10 Ag binding sites)
  • Efficient at complement fixation - MAC formation and target lysis
  • Efficient at forming defense Ab-pathogen complexes that are engulfed by macrophages
  • Secreted and membrane
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10
Q

IgG

A
  • effective at complement fixation
  • Mediate ADCC by NK cells
  • Enhancing phagocytosis by macrophages
  • secreted
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11
Q

IgA

A
  • Found in secretion (mucus, milk, tears, saliva)
  • effective at neutralizing toxins and pathogens
  • Does not fix complement so does not drive inflammation
  • protease-resistant, generally has long half-life in secretions
  • secreted
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12
Q

IgE

A
  • Best known for role in allergy and asthma
  • may also play a role in protection against parasitic helminths and protozoa
  • Made in very small quantities but induce potent effects
  • degranulation of eosinophils/basophils
  • release of molecules such as histamine to damage large pathogens
  • secreted
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13
Q

IgD

A
  • minor immunoglobulin
  • present in upper respiratory secretion (respiratory bacterial and viral pathogens)
  • binds basophils and mast cells and stimulates release of antimicrobial peptides
  • secreted and membrane
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14
Q

Fc receptors

A

mediate many effector functions of Ab

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15
Q

FCR signaling

A
  • multiple FcRs need to be cross-linked in order to initiate a signal
  • signal may be positive (enhancing) or negative (inhibiting)
  • Outcome depends on whether receptor is associated with ITAM or ITIM
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16
Q

FC(lambda)R

A
  • most diverse group of FcRs; four families in total
  • Main mediator of Ab functions in the body
  • Expressed by a wide range of cells
  • Most are activating receptors (will induce phagocytosis if expressed by macrophages, will induce degranulation If expressed by cytotoxic cells)
17
Q

Fc(epsilon)R

A
  • Expressed by granulocytes (mast cells/basophils, eosinophils)
  • Triggers a signaling cascade that releases histamines, proteases, and other inflammatory mediators
  • Most often associated with allergy symptoms
18
Q

PolyIgR

A
  • Polymeric immunoglobulin receptor
  • Expressed by epithelial cells
  • initiates transport of IgA and IgM from blood to the lumen of multiple tissues (Gastrointestinal tract, respiratory tract, reproductive tract)
  • Responsible for carrying Ab into tears and milk and populating gut music with IgA Ab to protect against ingested microbes and toxins
19
Q

Plasma cell-secreted Ab is carried to various body sites for isotope-specific effector function

A
  • opsonizing pathogens for phagocytosis
  • Activating complement cascades for pathogen lysis
  • Enhancing inflammatory activity of neutrophils
  • recruiting cytotoxic cells
  • recruiting and activating NK cells or ADCC killing
20
Q

Humoral immunity

A
  • combats pathogens via antibodies
  • antibodies produced by B cells
  • Antibodies can be transferred between individuals to provide passive immunity
21
Q

Cell-mediated

A
  • involves primarily T lymphocytes
22
Q

CTLs

A

recognize and kill infected/tumor cells via TCR activation

23
Q

Effector CTL generation from CTL precursors

A
1- TCR binds peptide presented by APC on MHC class 1
2- Co-stimulatory signal transmitted by CD28-B7 interactions between T cell and APC
3- IL-2, inducing proliferation and differentiation into CTL form
24
Q

CTLs recognize and kill infected or tumor cells by inducing apoptosis in target cells by

A
  1. intrinsic pathway-directional release of cytotoxic granules (perforin/granzyme B)
  2. Extrinsic pathway- ligand engagement (Fas-FasL)
25
Perfornin
pore-forming protein
26
Granzyme
serine protease
27
Intrinsic pathway
- When stimulated, CTLs release cytotoxic granule contents - both proteins are taken up by endocytic processes then punch holes in target cell membranes and induce apoptosis from the inside
28
Extrinsic Pathway
is mediated by the activation of death receptors by extracellular ligands. Engagement of ligand stimulated apoptosis in receptor-bearing cells - Fas-FasL pathway
29
Missing self model
NK cells recognize and kill infected cells and tumor cells by their absence of MHC class 1
30
How do NK cells recognize target (normal cells)?
- Normal cells present a ligand for the activating (killing) receptor on NK cells and an MHC class 1 ligand for the inhibitory receptors
31
How do NK cells recognize target (viruses)?
When viruses infect cells, some may inhibit MHC class 1 expression to evade detection and elimination by CTLs
32
How do NK cells recognize target (balance)?
the balance of inhibitory vs activating signals determines whether NK is activated or not