Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences
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Memory in the B–cell compartment: antibody affinity maturation

Michael S. Neuberger

Michael S. Neuberger

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

[email protected]

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Michael R. Ehrenstein

Michael R. Ehrenstein

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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Cristina Rada

Cristina Rada

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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Julian Sale

Julian Sale

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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Facundo D. Batista

Facundo D. Batista

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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Gareth Williams

Gareth Williams

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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and
Cesar Milstein

Cesar Milstein

Medical Resarch Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, UK

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    In the humoral arm of the immune system, the memory response is not only more quickly elicited and of greater magnitude than the primary response, but it is also different in quality. In the recall response to antigen, the antibodies produced are of higher affinity and of different isotype (typically immunoglobulin G rather than immunoglobulin M). This maturation rests on the antigen dependence of B–cell maturation and is effected by programmed genetic modifications of the immunoglobulin gene loci. Here we consider how the B–cell response to antigen depends on the affinity of the antigen–receptor interaction. We also compare and draw parallels between the two processes, which underpin the generation of secondaryresponse antibodies: V gene somatic hypermutation and immunoglobulin heavy–chain class switching.