直接受体:T和B淋巴细胞之间的受体相互作用:克隆辅助T细胞受体的抗体反应的独特型限制。

C A Janeway, B Broughton, L A Smith, T N Marion, K Bottomly
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引用次数: 0

摘要

免疫网络的概念包括T淋巴细胞和B淋巴细胞上受体之间相互作用的可能性,这种相互作用如果发生,可能会影响每组细胞中的受体库。事实上,B细胞独特型特异性辅助性T细胞,无论是mhc限制性的还是mhc非限制性的,已经被报道并被证明会影响B细胞库的表达。同样,有报道称B细胞可能影响调节性和mhc限制性T细胞的特异性。然而,克隆的mhc限制性辅助性T细胞和B细胞上受体之间的相互作用很难被记录下来。最近,我们利用一种不寻常的克隆辅助T细胞系来证明抗T细胞受体抗体是由T淋巴细胞和B淋巴细胞之间的直接受体相互作用产生的,并且这些相互作用不受MHC的限制。然而,这些早期的研究并没有解决这样的问题,即这种相互作用是否会导致表达多种不同抗体的B细胞活化,或者直接的T细胞受体:B细胞受体相互作用是否会导致独特的限制性B细胞反应。为了解决这个问题,我们现在研究了对传统的mhc限制性克隆T细胞系受体的单克隆和多克隆反应,并表明这些反应具有有限的独特型异质性。事实上,针对这一克隆细胞系的受体产生的约60%的抗体共享独特型决定因子,并且似乎识别受体上的单个表位。独特不相关的抗受体抗体,虽然仍然对克隆系具有特异性,但可以识别受体上明显的表位。这些数据提出了几个结论。首先,他们进一步证明了辅助性T细胞和B细胞之间的直接受体相互作用可以发生,并且可以相互刺激两种细胞类型。其次,如前所述,这种相互作用不受MHC的限制。第三,这种相互作用可能导致独特的限制性B细胞反应。最后,将这些结果与其他研究独特型特异性辅助性T细胞的研究人员的结果进行比较是很有趣的。由于本研究中使用的克隆系是一种传统的、MHC受限的、抗原特异性辅助性T细胞,携带α: β异二聚体受体复合物,并且由于其与B细胞的相互作用不受MHC限制,并导致独特型限制性抗体反应,因此可能会提出这些细胞是独特型特异性辅助性克隆的候选细胞。(摘要删节为400字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Direct receptor:receptor interactions between T and B lymphocytes: idiotypic restriction in the antibody response to a cloned helper T cell receptor.

The concept of an immunological network includes the possibility of interactions between receptors on T and B lymphocytes, and such interactions, should they occur, might be expected to influence the repertoire of receptors in each set of cells. Indeed, B cell idiotype specific helper T cells, both MHC-restricted and MHC-unrestricted, have been reported and have been shown to influence the expression of the B cell repertoire. Likewise, it has been reported that B cells may influence the specificity of both regulatory and MHC-restricted T cells. However, interactions between receptors on cloned, MHC-restricted helper T cells and B cells have been difficult to document. Recently, we have taken advantage of an unusual cloned helper T cell line to demonstrate that anti-T cell receptor antibody is produced by direct receptor:receptor interactions between T and B lymphocytes, and that these interactions are not MHC restricted. However, these earlier studies did not address the question of whether such interactions led to activation of B cells expressing multiple distinct antibodies, or whether direct T cell receptor:B cell receptor interactions would lead to an idiotypically restricted B cell response. To address this question, we have now examined both monoclonal and polyclonal responses to the receptor of a conventional, MHC-restricted cloned T cell line, and have shown that these responses are of limited idiotype heterogeneity. Indeed, about 60% of antibodies produced to the receptor of this cloned line share idiotypic determinants, and appear to recognize a single epitope on the receptor. Idiotypically unrelated anti-receptor antibodies, although still specific for the cloned line, recognize what appears to be a distinct epitope on the receptor. These data suggest several conclusions. First, they demonstrate further that direct receptor:receptor interactions between helper T cells and B cells can occur, and can be mutually stimulatory for the two cell types. Second, as shown previously, such interactions are not MHC restricted. Third, such interactions can lead to an idiotypically restricted B cell response. Finally, it is interesting to compared these results with those of other investigators studying idiotype-specific helper T cells. As the cloned line used in this study is a conventional, MHC-restricted, antigen specific helper T cell bearing an alpha:beta heterodimeric receptor complex, and as its interaction with B cells is MHC unrestricted and leads to idiotypically restricted antibody responses, one might propose that such cells are candidates for a clone of an idiotype-specific helper.(ABSTRACT TRUNCATED AT 400 WORDS)

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