B cells: Development, activation and humoral immunity Flashcards
B-cell development:
B cells develop in the bone marrow, where they undergo selection processes to ensure self-tolerance.
Bone marrow selection:
B cells that bind self-antigens with high affinity are eliminated to prevent autoimmunity.
B-cell receptor (BCR):
A membrane-bound antibody that allows B cells to recognize specific antigens.
Naïve B cells:
Mature B cells that have not yet encountered their specific antigen.
B-cell activation:
Occurs when the BCR binds to its specific antigen, and co-stimulatory signals from helper T cells are provided.
Helper T-cell support for B cells:
Activated CD4+ T cells provide cytokines and co-stimulatory signals that help B cells proliferate and differentiate.
Clonal expansion of B cells:
Activated B cells proliferate, creating a population of identical cells to combat the antigen.
B-cell differentiation:
Activated B cells differentiate into plasma cells (antibody-secreting cells) and memory B cells.
Plasma cells:
Differentiated B cells that secrete large amounts of antibodies specific to the antigen.
Antibody production:
Plasma cells produce antibodies (immunoglobulins) that bind to antigens, neutralize them, or mark them for destruction.
Humoral immunity:
The immune response mediated by antibodies produced by B cells, targeting pathogens and toxins.
Isotype switching:
B cells can change the class of antibody they produce (e.g., from IgM to IgG) in response to cytokine signals.
Memory B cells:
Long-lived B cells that remain after infection resolution, providing rapid antibody production upon re-exposure to the same antigen.
Antigen presentation by B cells:
B cells can act as antigen-presenting cells (APCs), presenting processed antigen to helper T cells to enhance activation.
T-independent activation:
Some antigens, like polysaccharides, can activate B cells without T cell help, though this response is weaker and lacks memory.