In order for B cells to respond to most antigens they require T cell help
TRUE OR FALSE
TRUE
B and T cells recognise the same antigen
TRUE OR FALSE
TRUE
T cells provide help to B cells in 2 ways:
Class Switching:
All B cells begin by making IgM.
IgG, IgA, and IgE isotypes are generated by an irreversible change in DNA in a process known as isotype switching/class switching.
Association of VH exon with different CH genes. Occurs through mechanism of nonhomologous DNA recombination guided by stretches of repetitive DNA called switch regions.
Switch regions contain repeats of GAGCT and GGGGGT sequences
Example of Class Switching: Switching from IgM (and IgD) to IgG1 expression
Distribution of antibody classes in the body:
Mothers provide protective antibodies to their young before birth only
TRUE OR FALSE
FALSE
Mothers provide protective antibodies to their young, both before and after birth
During pregnancy, IgG from maternal circulation is transported across the placenta.
After birth, GI tract of baby is protected by dimeric IgA in breast milk.
In first year of life infants have transient decrease in IgG levels as they slowly begin to produce their own IgG.
Neutralising antibodies:
IgG and IgA are examples of neutralising antibodies because they efficient at binding to soluble toxins and preventing them from binding to cell surface receptors (i.e. neutralising their effects).
neutralising antibodies can prevent bacterial infections and also prevent viruses from infecting host cells.
IgG:
IgM
Binding of IgM to antigen on a pathogen’s surface activates complement by the BLANK pathway
Binding of IgM to antigen on a pathogen’s surface activates complement by the classical pathway
Conformational change on binding to antigenic surface prevents inappropriate complement activation by free IgM
Conformational change:
“Planar” -> “Staple” conformation
Activation of classical complement pathway by IgG:
IgG Fab arms bound to antigenic surface
One C1q binds to 2 (or more) IgG molecules.
Requirement for interaction with two or more IgG molecules simultaneously prevents inappropriate complement activation by free IgG.
IgG subclasses ability to activate complement: IgG1: +++ IgG2: +/- IgG3: +++ IgG4: -
FcRn:
A human receptor for IgG Subunits: α1, α2, α3, β2 microglobulin (structurally similar to MHC class 1) Site that binds to IgG Fc region predominantly formed by α1 and α2 domains
Maintains high level of IgG in extracellular fluids
Selectively protects IgG from degradation that turns over other plasma proteins.
As a result, IgG molecules have a longer half-life than most plasma proteins (about 21 days)
FcRn is in part responsible for transport of IgG across placenta
FcRn transports IgG from bloodstream into extracellular spaces
FcRn interacts with the Fc interdomain region of IgG
FcγR:
IgG Receptors: FcγRI, FcγRII, FcγRIII
γ chain possesses signalling motif - ITAM (Immunoreceptor Tyrosine-based Activation Motif)
Human IgG subclasses have differing abilities to bind to and trigger via FcγR
FcγRI is the receptor for IgG1 and IgG3.
FcγRI binds to the lower hinge and CH2 of IgG3.
IgG3 bound to FcγRI binds antigen.
Fc receptor-mediated clearance:
Free Ig does not cross-link Fc receptors = No macrophage activation
Aggregation of Ig on bacterial surface results in cross-linking of Fc receptors = Macrophage activation (and phagocytosis)
Fc receptor ligation enhances the efficiency of phagocytosis
IgD:
Heavily Glycosylated
Found at very low serum concentrations
Found instead on surface of lymphocytes
Function unclear but may be involved in control of Ab response