Regulation of germinal center B-cell differentiation
Summary Germinal centers (GC) are the main sites where antigen‐activated B‐cell clones expand and undergo immunoglobulin gene hypermutation and selection. Iterations of this process will lead to affinity maturation, replicating Darwinian evolution on the cellular level. GC B‐cell selection can lead...
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Published in | Immunological reviews Vol. 270; no. 1; pp. 8 - 19 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
England
Blackwell Publishing Ltd
01.03.2016
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Summary
Germinal centers (GC) are the main sites where antigen‐activated B‐cell clones expand and undergo immunoglobulin gene hypermutation and selection. Iterations of this process will lead to affinity maturation, replicating Darwinian evolution on the cellular level. GC B‐cell selection can lead to four different outcomes: further expansion and evolution, apoptosis (non‐selection), or output from the GC with differentiation into memory B cells or plasma cells. T‐helper cells in GC have been shown to have a central role in regulating B‐cell selection by sensing the density of major histocompatibility complex (MHC):peptide antigen complexes. Antigen is provided on follicular dendritic cells in the form of immune complex. Antibody on these immune complexes regulates antigen accessibility by shielding antigen from B‐cell receptor access. Replacement of antibody on immune complexes by antibody generated from GC‐derived plasma cell output will gradually reduce the availability of antigen. This antibody feedback can lead to a situation where a slow rise in selection stringency caused by a changing environment leads to directional evolution toward higher affinity antibody. |
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Bibliography: | ark:/67375/WNG-DH371BHD-1 ArticleID:IMR12396 istex:0D0528F011996C3EA90C8F11101D948AE6D00CB6 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 0105-2896 1600-065X 1600-065X |
DOI: | 10.1111/imr.12396 |