J δ 3基因片段在克罗恩病中的过度利用

S B Landau, C S Probert, C A Stevens, S P Balk, R S Blumberg
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引用次数: 0

摘要

大多数正常人肠道上皮内淋巴细胞(iIEL)是CD8+,表达α - β - t细胞受体(TCR),并且是寡克隆的。其余的正常iels也是寡克隆的,它们表达γ δ - tcr,并优先利用与成人外周血淋巴细胞(V δ 2)不同的可变区(V δ 1和V δ 3)。γ δ - tcr在肠道疾病中的连接区使用情况在很大程度上是未知的。本研究的目的是通过聚合酶链反应扩增、克隆和测序,比较克罗恩病(CD)中γ δ t细胞的克隆性和V δ 1和V δ 3转录本的连接区使用情况,并与其他几种慢性炎症性疾病进行比较。正如之前在正常受试者中观察到的,所有炎症病例,包括CD (n = 3)、溃疡性结肠炎(n = 1)、憩室炎(n = 1)和淋巴细胞性结肠炎(n = 1), V δ 1和V δ 3转录本包含重复序列,与表达这些受体的γ δ t细胞的扩增一致。在2/3的乳糜泻病例中,但在非乳糜泻炎症病例中,在V δ 1和/或V δ 3转录本中观察到含有J δ 3的转录本,这是一种很少使用的J δ。因此,在CD的一个亚群中,表达J δ 3的γ δ -T细胞可能会扩增,这意味着独特的配体可以驱动表达这些受体的T细胞扩增。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Over-utilization of the J delta 3 gene-segment in Crohn's disease.

A majority of normal human intestinal intraepithelial lymphocytes (iIEL) are CD8+, express the alpha beta-T cell receptor (TCR) and are oligoclonal. The remainder of normal iIELs, which are also oligoclonal, express the gamma delta-TCR and preferentially utilize variable regions (V delta 1 and V delta 3) which are different from adult peripheral blood lymphocytes (V delta 2). The junctional region usage of gamma delta-TCRs in intestinal diseases is largely unknown. The aim of this study was to examine gamma delta-T cell clonality and junctional region usage of V delta 1 and V delta 3 transcripts in Crohn's Disease (CD) in comparison to several other chronic inflammatory diseases of the colon by polymerase chain reaction amplification, cloning and sequencing. As previously observed in normal subjects, all inflammatory cases examined, including CD (n = 3), ulcerative colitis (n = 1), diverticulitis (n = 1) and lymphocytic colitis (n = 1), the V delta 1 and V delta 3 transcripts contained reiterated sequences consistent with the expansion of gamma delta-T cells expressing these receptors. In 2/3 CD cases, but none of the non-CD inflammatory cases, transcripts containing J delta 3, a rarely used J delta, was observed among the V delta 1 and/or V delta 3 transcripts. Thus, in a subset of CD, gamma delta-T cells expressing J delta 3 may be expanded implicating a role for unique ligands that drive the expansion of T cells expressing these receptors.

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