| Literature DB >> 26118840 |
K-P Nera1, M K Kyläniemi1, O Lassila1.
Abstract
Persistent humoral immunity depends on the follicular B cell response and on the generation of somatically mutated high-affinity plasma cells and memory B cells. Upon activation by an antigen, cognately activated follicular B cells and follicular T helper (TFH ) cells initiate germinal centre (GC) reaction during which high-affinity effector cells are generated. The differentiation of activated follicular B cells into plasma cells and memory B cells is guided by complex selection events, both at the cellular and molecular level. The transition of B cell into a plasma cell during the GC response involves alterations in the microenvironment and developmental state of the cell, which are guided by cell-extrinsic signals. The developmental cell fate decisions in response to these signals are coordinated by cell-intrinsic gene regulatory network functioning at epigenetic, transcriptional and post-transcriptional levels.Mesh:
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Year: 2015 PMID: 26118840 DOI: 10.1111/sji.12336
Source DB: PubMed Journal: Scand J Immunol ISSN: 0300-9475 Impact factor: 3.487