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Antigen Receptor Allelic Exclusion: An Update and Reappraisal

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JOURNAL OF IMMUNOLOGY
卷 185, 期 7, 页码 3801-3808

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1001158

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  1. University of Pennsylvania [TG GM-07229]
  2. Department of Pathology and Laboratory Medicine
  3. Center for Childhood Cancer Research of the Children's Hospital of Philadelphia
  4. Abramson Family Cancer Research Institute of the University of Pennsylvania School of Medicine
  5. National Institutes of Health [R01 CA125195]
  6. NATIONAL CANCER INSTITUTE [R01CA125195] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [T32GM007229] Funding Source: NIH RePORTER

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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.

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