Antigen Receptor Allelic Exclusion: An Update and Reappraisal

被引:101
作者
Brady, Brenna L. [1 ]
Steinel, Natalie C. [1 ]
Bassing, Craig H. [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia,Ctr Childhood Canc Re, Div Canc Pathobiol,Abramson Family Canc Res Inst, Immunol Grad Grp,Dept Pathol & Lab Med,Sch Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
T-CELL-RECEPTOR; CHROMOSOMAL V(D)J RECOMBINATION; IMMUNOGLOBULIN-KAPPA LOCUS; DOUBLE-STRAND BREAKS; TCR-BETA LOCUS; B-CELLS; LYMPHOCYTE DEVELOPMENT; GENE-EXPRESSION; LIGHT-CHAIN; V-H;
D O I
10.4049/jimmunol.1001158
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Most lymphocytes express cell surface Ag receptor chains from single alleles of distinct Ig or TCR loci. Since the identification of Ag receptor allelic exclusion, the importance of this process and the precise molecular mechanisms by which it is achieved have remained enigmatic. This brief review summarizes current knowledge of the extent to which Ig and TCR loci are subject to allelic exclusion. Recent progress in studying and defining mechanistic steps and molecules that may control the monoallelic initiation and subsequent inhibition of V-to-(D)-J recombination is outlined using the mouse TCR beta locus as a model with frequent comparisons to the mouse IgH and Ig kappa loci. Potential consequences of defects in mechanisms that control Ag receptor allelic exclusion and a reappraisal of the physiologic relevance of this immunologic process also are discussed. The Journal of Immunology, 2010, 185: 3801-3808.
引用
收藏
页码:3801 / 3808
页数:8
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