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独特型诱导的T细胞刺激需要与HLA - DR分子相关联的抗原呈递。

Idiotype-induced T cell stimulation requires antigen presentation in association with HLA-DR molecules.

作者信息

Yi Q, Holm G, Lefvert A K

机构信息

Immunological Research Laboratory, Karolinska Hospital, Stockholm, Sweden.

出版信息

Clin Exp Immunol. 1996 May;104(2):359-65. doi: 10.1046/j.1365-2249.1996.27735.x.

Abstract

An important and yet unresolved question concerns the mode of T cell recognition of idiotypic epitopes on immunoglobulin molecules in humans. Results from murine and human studies show that some idiotype-specific T cells recognize conformational epitopes on immunoglobulin, and such T cells are not MHC-restricted. In the present study T cell stimulation induced by idiotypic determinants on the autologous monoclonal IgG (M-components) from patients with monoclonal gammopathies was studied. In parallel, T cell stimulation in response to a conventional antigen, purified protein derivative, was also examined. It is shown that, as with conventional antigen, idiotype-induced T cell stimulation requires the presence of antigen-presenting cells (APC; monocytes and/or B cells), and is MHC class II (DR)-restricted. B cells, but not monocytes, can present idiotypic determinants to T cells at very low antigen concentrations, while monocytes do so only when antigen is present at high concentrations. Antigen processing and presentation is abrogated by treatment of APC with chloroquine. In conclusion, our study demonstrates that human idiotype-specific T cells recognize processed idiotypic determinants presented by MHC class II (HLA-DR) molecules on APC, and that B cells require about 1000-fold less antigen that monocytes.

摘要

一个重要但尚未解决的问题涉及人类T细胞对免疫球蛋白分子独特型表位的识别模式。小鼠和人类研究的结果表明,一些独特型特异性T细胞识别免疫球蛋白上的构象表位,并且此类T细胞不受MHC限制。在本研究中,对来自单克隆丙种球蛋白病患者的自体单克隆IgG(M成分)上独特型决定簇诱导的T细胞刺激进行了研究。同时,也检测了对传统抗原纯化蛋白衍生物的T细胞刺激反应。结果表明,与传统抗原一样,独特型诱导的T细胞刺激需要抗原呈递细胞(APC;单核细胞和/或B细胞)的存在,并且受MHC II类(DR)限制。B细胞而非单核细胞能够在极低抗原浓度下将独特型决定簇呈递给T细胞,而单核细胞只有在抗原浓度较高时才会这样做。用氯喹处理APC会消除抗原加工和呈递。总之,我们的研究表明,人类独特型特异性T细胞识别由APC上的MHC II类(HLA-DR)分子呈递的加工后的独特型决定簇,并且B细胞所需的抗原量比单核细胞少约1000倍。

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