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由克隆的同种反应性T细胞定义的DQw3变体。

DQw3 variants defined by cloned alloreactive T cells.

作者信息

Mickelson E M, Nepom G T, Nisperos B, Hansen J A

机构信息

Histocompatibility Laboratories, Fred Hutchinson Cancer Research Center, Seattle, WA 98104.

出版信息

Hum Immunol. 1988 Jan;21(1):63-73. doi: 10.1016/0198-8859(88)90081-x.

Abstract

The polymorphism of HLA class II molecules expressing the serologically defined alloantigen DQw3 was studied using cloned proliferative T lymphocytes. Two clones, IG9 and IC3, were selectively primed against DQw3-associated determinants and tested against a panel of 92 HLA-D homozygous cells. Both clones were specific for DQw3, but each showed a distinct response pattern. Clone IG9 recognized a DQw3-associated determinant expressed on a subset of DR4 and DR5 haplotypes and on all DRw6, 7, w8, and w9 haplotypes tested. In contrast, clone IC3 recognized a distinct DQw3-associated determinant expressed only on a subset of DR4 haplotypes. In monoclonal antibody inhibition experiments, anti-DQ, but not anti-DR or anti-DP antibodies, blocked reactivity of both clones IG9 and IC3, further demonstrating that the determinants defined by these clones are associated with DQ molecules. In DNA hybridization studies using a DQ beta probe, a correlation was observed between restriction site polymorphisms in the DQ beta gene, designated DQw"3.1" and "3.2," and the expression of the T-cell-defined IG9 and IC3 determinants. It is, thus, possible to demonstrate by cloned T-cell reactivity functionally relevant recognition sites on DQw3+ molecules that are associated with structural polymorphisms defined by molecular and genomic analysis.

摘要

利用克隆的增殖性T淋巴细胞研究了表达血清学定义的同种异体抗原DQw3的HLA II类分子的多态性。两个克隆,IG9和IC3,被选择性地针对与DQw3相关的决定簇进行致敏,并针对一组92个HLA - D纯合细胞进行检测。两个克隆均对DQw3具有特异性,但每个克隆都表现出独特的反应模式。克隆IG9识别在DR4和DR5单倍型的一个亚群以及所有测试的DRw6、7、w8和w9单倍型上表达的与DQw3相关的决定簇。相比之下,克隆IC3识别仅在DR4单倍型的一个亚群上表达的独特的与DQw3相关的决定簇。在单克隆抗体抑制实验中,抗DQ抗体而非抗DR或抗DP抗体阻断了克隆IG9和IC3的反应性,进一步证明这些克隆所定义的决定簇与DQ分子相关。在使用DQβ探针的DNA杂交研究中,观察到DQβ基因中指定为DQw“3.1”和“3.2”的限制性位点多态性与T细胞定义的IG9和IC3决定簇的表达之间存在相关性。因此,通过克隆的T细胞反应性可以证明DQw3 +分子上与分子和基因组分析所定义的结构多态性相关的功能相关识别位点。

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