Evaluate the clonal selection hypothesis in terms of autoimmunity and
immunological memory.
Clonal selection is the theory that lymphocytes have antigen receptors before they are activated, and that spontaneous mutations during clonal expansion lead to lymphocytes with high antigen-binding affinities. It is a theory that a single lymphocyte (specifically, a B cell) expresses antigen-specific receptors that are determined before the antibody ever meets the antigen. As Ag binds to a chromosome, it stimulates it, allowing clone daughter cells to proliferate.
Negative selection in the bone marrow produces central tolerance in B cells. Before leaving the bone marrow, immature B cells are screened for auto-reactivity. Immature B cells with BCRs that bind to self-antigens too strongly will not be destroyed. Random mutations during clonal expansion induce the development of B cells with an improved antibody-binding affinity for their antigens during clonal selection. The clonal selection hypothesis could understand why secondary immune responses are so effective in avoiding reinfection by the same pathogen.
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