Lymphocytes that develop in bone marrow.
Express unique antigen receptors (BCR or secreted antibody).
Plasma cells are activated B cells which secrete antibodies.
Memory B cells provide immunological memory.
Each B cell surface has ~100,000 BCRs (mainly IgM / IgD antibodies).
BCR binds antigen, activating the B cell.
BCR is membrane-anchored via a transmembrane domain (TM); secreted antibodies lack a TM.
Neutralization
Opsonization (enhances phagocytosis)
Complement activation
Antibodies bind native antigens without needing MHC processing.
Epitope: Antibody binding site on an antigen.
IgG (monomer):
Most abundant in blood.
Opsonizes/neutralizes and targets viruses/bacteria.
Only Ig class to cross the placenta, providing 'passive immunity'.
IgA (dimer):
Present in secretions (tears, saliva, mucus, breast milk).
Defends mucous membranes, especially the gut.
Provides 'passive immunity' to nursing infants via breast milk.
Targets viruses/bacteria.
IgM (pentamer):
First Ig class produced after initial antigen exposure.
Expressed on naive B cells.
Effective in activating complement.
Targets extracellular bacteria.
Acts as antigen receptor (BCR).
IgE (monomer):
Low concentrations in blood.
Immunity to multicellular parasites.
Involved in allergic reactions, activating mast cells.
IgD (monomer):
Expressed on naive B cells.
Acts as antigen receptor (BCR) together with IgM; specific function largely unknown.
Antigen + T cell stimulation of B cells leads to plasma cell formation.
Some stimulated B cells form memory cells.
Persist for years in blood and lymphatic tissue.
Express antibody as BCR, but do not secrete it.
Respond rapidly to antigen encounter and become plasma cells.
Takes 7-14 days to produce sufficient antibody to eliminate the pathogen.
Relatively low antibody amount produced, mainly IgM.
Basis of vaccination success, relies on memory B cells.
Fast: 2-3 days to produce sufficient antibody to eliminate pathogen.
Mainly IgG, with class switching to IgA and IgE (low levels).