L16: Antibodies - structure, function, classes, Fc receptors Flashcards

1
Q

Subclasses of IgG and IgA in humans and mouse

A

Human: IgG1/G2/G3/G4 and IgA1/A2
Mouse: IgG1, G2a/G2b, G3

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2
Q

IgA

A

Dimer, transport mechanisms, front-line defence mechanism and mucosal secretion, transport across epithelium

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3
Q

IgG

A

Small molecule, can diffuse and cross placenta for newborn protection

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4
Q

IgE

A

High affinity for mast cells and lines blood cells and connective tissues

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5
Q

IgM

A

Restricted to circulatory system, pentamer

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6
Q

General antibody functions (5)

A
  1. Neutralisation
  2. Opsonisation
  3. Complement activation (opsonisation, direct killing, recruitment)
  4. ADCC (antibody-dependent cell-mediated cytotoxicity)
  5. Triggering of mast cells, basophils and activated eosinophils
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7
Q

Neutralisation

A

Doesn’t require Fc region, binds to epitope to prevent pathogen from delivering signal

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8
Q

Opsonisation

A

cluster of Fc regions bind to Fc receptors on macrophages:

  1. Bacterium is coated with complement and IgG antibody
  2. C3b binds to CR1 and antibody binds to Fc receptor, bacteria are phagocytosed
  3. Macrophage membranes fuse, creating a membrane-bounded vesicle, the phagosome
  4. Lysosomes fuse with these vesicles, delivering enzymes that degrade bacterium
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9
Q

ADCC

A

Mediated by NK cells which act through downregulated MHC1 or ADCC pathway. Fab region binds to target cell where NK cells recognise Fc regions of antibodies through Fc receptors.

  1. Antibody binds antigens on surface of target cells
  2. Fc receptors on NK cells recognise bound antibody
  3. Cross-linking of Fc receptors signals NK cell to kill the target cell
  4. Target cell dies by apoptosis
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10
Q

Mast Cell Activation

A

Occurs through Fc epsilon receptors which bind to IgE; potent inflammatory cells and secrete performed inflammatory mediators

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11
Q

Thymus-dependent or independent antigens

A

Thymus dependent (Th cells provide signal)
Signal 1: antigen binding to B cell receptor
Signal 2:
a) TI antigen: intrinsic second signal
b) TD antigen: cytokines and CD40L

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12
Q

BCR Gene Rearrangment (4)

A
  1. Occurs during development of naive B cell
  2. Occurs in bone marrow
  3. Antigen-independent
  4. Similar process occurs for TCR
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13
Q

Class switching (4)

A
  1. Occurs during mature IgM+ B cell activation
  2. Occurs in secondary lymphoid organs
  3. Antigen-dependent
  4. Unique to B cells
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14
Q

Somatic recombination in B cells

A
  1. Early B cells - generation of diversity of BCR occuring in bone marrow
  2. Mature B cells - isotype switching occuring in secondary lymphoid organs
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15
Q

Mechanisms of isotype switching (3)

A
  1. AID: activation-induced cytidine deaminase; conversion of cytosine to uridine
  2. UNG: uracil-DNA glycosylase; locks off the base, leaves single sugar
  3. APE1: apurinic/apyrimidinic endonuclease 1: removes sugar so ribose is open and nicked, enabling splicing out and ligation of DNA
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16
Q

Isotype/class switching signal failing

A

Requires Th cell signals: CD40L and cytokines. If signals don’t work due to genetic defects: Hyper-IgM syndome (high IgM, low levels of Igs) results in infection susceptibility. Syndrome can result in deficiency in Th cell function or B cell machinery

17
Q

Link between IgG sub-classes & Th1/Th2 responses: Intracellular vs Extracellular pathogen control

A

Th1 responses: resistance to intracellular pathogens (macrophage activation)
Th2 responses: susceptibility to intracellular pathogens (macrophage deactivation), resistance to large extracellular pathogens (allergy-type response)

18
Q

Link between IgG sub-classes & Th1/Th2 responses: Macrophage regulation

A

Th1:
1. IgG2a - interacts with FcyR1, activating receptor and macrophage activation
2. IFN-y cytokine, increases FcyR1 expression, more tissue damage, effective intracellular pathogen celarance
Th2:
1. IgG1 - interats with FcyR2B, inhibitory receptor, macrophage deactivation
2. IL-4 cytokine, increases FcyR2B expression, less tissue damage, ineffective intracellular pathogen celarance