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T细胞受体基因及其与人类疾病的关联。

The T cell receptor gene and its association with human diseases.

作者信息

Klig S, Chiaramonte L, Verma R S

机构信息

Division of Genetics, Long Island College Hospital-SUNY Health Science Center, Brooklyn 11201.

出版信息

Exp Clin Immunogenet. 1992;9(3):117-24.

PMID:1303091
Abstract

The genetic organization and protein structure of the T cell receptor (TCR)/CD3 complex are currently under investigation, and recent work has provided information about its assembly, expression and function. This article reviews what is currently known about the structure and assembly of the TCR/CD3 complex. The TCR chains are members of the immunoglobulin gene superfamily and are generated by combinatorial associations of V, J, D, and C genes. The presence of certain gene rearrangements within these chains has been associated with lymphoproliferative disorders, autoimmune disease and immunodeficiencies. TCR rearrangements can be useful in the diagnosis of lymphoproliferative disorders and in the identification of patients who will subsequently relapse, once in remission. With respect to autoimmune disease, the possibility now exists of immunotherapy with TCR designer polypeptides to prevent disease. In patients with primary immunodeficiencies secondary to defects in expression of the TCR, the possibility of somatic gene therapy now exists. As more information unfolds about the role that TCR gene rearrangements have in various diseases, new insights are gained into better diagnosis and treatment.

摘要

T细胞受体(TCR)/CD3复合物的基因组织和蛋白质结构目前正在研究中,近期的研究工作已提供了有关其组装、表达和功能的信息。本文综述了目前已知的TCR/CD3复合物的结构和组装情况。TCR链是免疫球蛋白基因超家族的成员,由V、J、D和C基因的组合关联产生。这些链内某些基因重排的存在与淋巴增殖性疾病、自身免疫性疾病和免疫缺陷有关。TCR重排在淋巴增殖性疾病的诊断以及缓解后可能复发的患者的识别中可能有用。关于自身免疫性疾病,现在存在用TCR设计多肽进行免疫治疗以预防疾病的可能性。在因TCR表达缺陷继发原发性免疫缺陷的患者中,现在存在进行体细胞基因治疗的可能性。随着越来越多关于TCR基因重排在各种疾病中作用的信息被揭示,人们对更好的诊断和治疗有了新的认识。

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