共 200 条
B cell receptor editing in tolerance and autoimmunity
被引:58
作者:
Prak, Eline T. Luning
[1
]
Monestier, Marc
[2
]
Eisenberg, Robert A.
[3
]
机构:
[1] Univ Penn, Dept Pathol & Lab Med, Stellar Chance Labs 405B, Sch Med, Philadelphia, PA 19104 USA
[2] Temple Univ, Sch Med, Dept Microbiol & Immunol, Temple Autoimmun Ctr, Philadelphia, PA 19122 USA
[3] Univ Penn, Sch Med, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA
来源:
YEAR IN IMMUNOLOGY
|
2011年
/
1217卷
关键词:
receptor editing;
antibody;
autoimmunity;
B cell;
V(D)J recombination;
LIGHT-CHAIN GENES;
SYSTEMIC-LUPUS-ERYTHEMATOSUS;
GRAFT-VERSUS-HOST;
IMMUNOGLOBULIN-KAPPA-CHAIN;
ANTI-DNA ANTIBODIES;
RECOMBINATION-ACTIVATING GENES;
HIGH-AFFINITY AUTOANTIBODIES;
MURINE LEUKEMIA-VIRUS;
V-H REPLACEMENT;
HEAVY-CHAIN;
D O I:
10.1111/j.1749-6632.2010.05877.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Receptor editing is the process of ongoing antibody gene rearrangement in a lymphocyte that already has a functional antigen receptor. The expression of a functional antigen receptor will normally terminate further rearrangement (allelic exclusion). However, lymphocytes with autoreactive receptors have a chance at escaping negative regulation by "editing" the specificities of their receptors with additional antibody gene rearrangements. As such, editing complicates the Clonal Selection Hypothesis because edited cells are not simply endowed for life with a single, invariant antigen receptor. Furthermore, if the initial immunoglobulin gene is not inactivated during the editing process, allelic exclusion is violated and the B cell can exhibit two specificities. Here, we describe the discovery of editing, the pathways of receptor editing at the heavy (H) and light (L) chain loci, and current evidence regarding how and where editing happens and what effects it has on the antibody repertoire.
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页码:96 / 121
页数:26
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