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使用破伤风毒素特异性T细胞克隆对血清学DR LYGUE和基因型DRB1*1303特异性进行功能剖析。

Functional dissection of the serological DR LYGUE and genotypic DRB1*1303 specificities using a tetanus toxin-specific T-cell clone.

作者信息

Martínez-Soria E, Tiercy J M, Beffy P, Taban-Marín P, Jaques D, Bétuel H, Jeannet M, Mach B, Irlé C

机构信息

Department of Genetics and Microbiology, University of Geneva Medicine School, Switzerland.

出版信息

Tissue Antigens. 1993 Sep;42(3):118-24. doi: 10.1111/j.1399-0039.1993.tb02177.x.

Abstract

The DRB1 sequence of the homozygous cell line HAG (DR13-DwHAG-DQ7) represents a new DRB allele assigned DRB11103, whereas its DRB3 sequence corresponds to the previously described DRB30101 (DR52a) allele. The DRB11303 gene product is undetectable by current sera used in routine serology typing. We report here direct evidence that the MHC molecule encoded by the DRB11303 gene is functional in antigen presentation and in T-cell restriction. We describe a T-cell clone specific for tetanus toxin whose restriction pattern strictly follows the DRB11303 allele, as defined by oligonucleotide typing. It also follows the serologic reactivity with the serum LYGUE and also the DwHAG MLC-defined specificity pattern, with one exception. The potential functional sites for the DRB11303 gene product involved in T-cell restriction were deduced from sequence comparisons between DRB11303 and closely related DRB1 alleles. The relevant as substitutions were located within close proximity to each other on the HLA class II structural model. Our results demonstrate that 1) DRB11303 is functional in antigen presentation and T-cell restriction 2) the functional region involved in antigen presentation and T-cell restriction by DRB1*1303 can be defined structurally.

摘要

纯合细胞系HAG(DR13-DwHAG-DQ7)的DRB1序列代表一个新的DRB等位基因,被指定为DRB11103,而其DRB3序列对应于先前描述的DRB30101(DR52a)等位基因。目前常规血清学分型所用的血清无法检测到DRB11303基因产物。我们在此报告直接证据,表明由DRB11303基因编码的MHC分子在抗原呈递和T细胞限制性方面具有功能。我们描述了一个针对破伤风毒素的T细胞克隆,其限制性模式严格遵循由寡核苷酸分型定义的DRB11303等位基因。它也遵循与血清LYGUE的血清学反应性以及DwHAG MLC定义的特异性模式,但有一个例外。通过DRB11303与密切相关的DRB1等位基因之间的序列比较,推断出DRB11303基因产物中参与T细胞限制性的潜在功能位点。相关替代位于HLA II类结构模型上彼此紧邻的位置。我们的结果表明:1)DRB11303在抗原呈递和T细胞限制性方面具有功能;2)DRB1*1303参与抗原呈递和T细胞限制性的功能区域可以在结构上进行定义。

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