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逆转录病毒基因转移所证实的T细胞受体α链的免疫调节活性

Immunoregulatory activity of the T-cell receptor alpha chain demonstrated by retroviral gene transfer.

作者信息

Green D R, Bissonnette R, Zheng H G, Onda T, Echeverri F, Mogil R J, Steele J K, Voralia M, Fotedar A

机构信息

Department of Immunology, University of Alberta, Edmonton, Canada.

出版信息

Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8475-9. doi: 10.1073/pnas.88.19.8475.

Abstract

We have previously described an antigen-specific I-Ad-restricted T-cell hybridoma, A1.1, that constitutively releases an antigen-specific immunoregulatory activity into supernatants. Using retrovirally mediated gene transfer, we have found that transfer of the T-cell receptor alpha chain (TCR alpha) gene from A1.1 to a number of other T-cell hybridomas effectively transferred the ability to produce the activity. Gene transfer of the TCR beta chain (TCR beta), however, did not transfer this ability. The regulatory activity from cells expressing the A1.1 TCR alpha bound to and was eluted from an anti-TCR alpha monoclonal antibody and displayed fine antigenic specificity identical to that of supernatants from A1.1. The possibility that this activity represents a secreted form of the TCR alpha (as opposed to shed cell-surface TCR) was examined in BW1100 cells, lacking TCR alpha and TCR beta, which produced the antigen-specific activity after gene transfer of the A1.1 TCR alpha gene. The expression of the immunoregulatory activity in supernatants correlated with a direct antigen-binding activity as detected by ELISA, thus raising the possibility that antigen binding is relevant to the mechanism of action of the soluble TCR alpha. We discuss these observations and our earlier studies suggesting an immunoregulatory role for soluble TCR alpha.

摘要

我们之前描述过一种抗原特异性的、受I - Ad限制的T细胞杂交瘤A1.1,它能持续向培养上清中释放抗原特异性免疫调节活性物质。利用逆转录病毒介导的基因转移技术,我们发现将A1.1的T细胞受体α链(TCRα)基因转移到其他多种T细胞杂交瘤中,能有效地转移产生该活性物质的能力。然而,T细胞受体β链(TCRβ)的基因转移却不能转移这种能力。表达A1.1 TCRα的细胞所产生的调节活性物质能与抗TCRα单克隆抗体结合,并可从该抗体上洗脱下来,且其精细抗原特异性与A1.1培养上清中的活性物质相同。在缺乏TCRα和TCRβ的BW1100细胞中研究了这种活性物质是否代表TCRα的一种分泌形式(与脱落的细胞表面TCR相对),该细胞在转入A1.1 TCRα基因后产生了抗原特异性活性物质。培养上清中免疫调节活性物质的表达与ELISA检测到的直接抗原结合活性相关,因此增加了抗原结合与可溶性TCRα作用机制相关的可能性。我们讨论了这些观察结果以及我们早期的研究,这些研究提示了可溶性TCRα具有免疫调节作用。

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