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Author(s): McHeyzer-Williams LJ; McHeyzer-Williams MG
Title: Antigen-specific memory B cell development
Source: ANNUAL REVIEW OF IMMUNOLOGY 23: 487-513
Date: 2005
Document Type: Journal : Review
DOI:
Language: English
Comment:
Address: Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA.
Reprint: McHeyzer-Williams, LJ, Scripps Res Inst, Dept Immunol, 10666 N Torrey
Pines Rd, La Jolla, CA 92037 USA. E-mail: louisemw@scripps.edu
mcheyzer@scripps.edu Author Keywords: adaptive immunity; germinal centers; plasma cells; memory B cells;
multiple myeloma
KeyWords Plus: PRIMARY IMMUNE-RESPONSE; FOLLICULAR DENDRITIC CELLS; MARROW PLASMA-
CELLS; CD4 T-CELLS; TRANSCRIPTION FACTOR XBP-1; CLASS SWITCH
RECOMBINATION; LYMPHOTOXIN BETA-RECEPTOR; CYTIDINE DEAMINASE AID; TOLL-
LIKE RECEPTORS; CLASS-II COMPLEXES
Abstract: Helper T (Th) cell-regulated B cell immunity progresses in an ordered cascade of cellular development that culminates in the production of antigen-specific memory B cells. The recognition of peptide MHC class II complexes on activated antigen-presenting cells is critical for effective Th cell selection, clonal expansion, and effector Th cell function development (Phase I). Cognate effector Th cell-B cell interactions then promote the development of either short-lived plasma cells (PCs) or germinal centers (GCs) (Phase II). These GCs expand, diversify, and select high-affinity variants of antigen-specific B cells for entry into the long-lived memory B cell compartment (Phase III). Upon antigen rechallenge, memory B cells rapidly expand and differentiate into PCs under the cognate control of memory Th cells (Phase IV). We review the cellular and molecular regulators of this dynamic process with emphasis on the multiple memory B cell fates that develop in vivo.
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