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针对曼氏血吸虫保护性表位的抗独特型抗体特异性T细胞系的功能分析。I. 在抗曼氏血吸虫抗体应答中的作用。

Functional analysis of a T cell line specific for antiidiotypic antibodies to a Schistosoma mansoni protective epitope. I. Role in the anti-S. mansoni antibody response.

作者信息

Velge-Roussel F, Auriault C, Mazingue C, Capron A

机构信息

Centre d'Immunologie et de Biologie Parasitaire, Unité mixte INSERM U 167-CNRS 624, Institut Pasteur, Lille, France.

出版信息

J Immunol. 1991 Dec 1;147(11):3960-6.

PMID:1719095
Abstract

Previous data have shown that from an antiparasitic IgE mAb (mAb1), antianti-Id IgG and IgE antibodies (Ab3) could be prepared. These Ab3 demonstrated the same functional properties as the Ab1, such as in vitro cytotoxic activity toward schistosomula and in vivo a protective effect against Schistosoma mansoni infection. To study the possible interactions between the idiotypic network and the regulation of isotypic expression, we focused on Id-specific T cells obtained by immunization with Ab2. Both Ab2 idiotopes and native schistosomula Ag were able to stimulate the proliferation of anti-Ab2 T cells in vitro. The activation of anti-Ab2 T cells by Ab2 shared the classic characteristics of Th cells, namely, it was MHC-restricted and required APC. A T cell line could be maintained in long term culture by stimulation with schistosomula Ag. The adoptive transfer of cells from this line to 26-kDa Ag-immunized or S. mansoni-infected rats led to a dramatic increase in the specific humoral response. This effect was restricted to antibodies specific for 26- and 56-kDa Ag (the targets of the mAb1) and was observed for the two isotypes tested, i.e., IgG and IgE. Finally, the helper effect on the antibody response could be further amplified by cooperation of anti-Ab2 T cells with Id-specific cells of the first generation (anti-Ab1 cells). Together with Ag-specific Th cells, the Id-specific T cells may, due to their specificity and their functional properties, play a major role in the induction and more importantly, in the maintenance of the immune response.

摘要

先前的数据表明,从一种抗寄生虫IgE单克隆抗体(mAb1)可以制备抗独特型IgG和IgE抗体(Ab3)。这些Ab3表现出与Ab1相同的功能特性,例如对血吸虫童虫的体外细胞毒性活性以及对曼氏血吸虫感染的体内保护作用。为了研究独特型网络与同种型表达调节之间可能的相互作用,我们聚焦于用Ab2免疫获得的独特型特异性T细胞。Ab2独特型表位和天然血吸虫童虫抗原均能够在体外刺激抗Ab2 T细胞的增殖。Ab2对抗Ab2 T细胞的激活具有Th细胞的经典特征,即具有MHC限制性且需要抗原呈递细胞。通过用血吸虫童虫抗原刺激,可长期维持一个T细胞系。将该细胞系的细胞过继转移至用26-kDa抗原免疫或感染曼氏血吸虫的大鼠体内,导致特异性体液反应显著增强。这种效应仅限于对26-kDa和56-kDa抗原(mAb1的靶标)具有特异性的抗体,并且在所检测的两种同种型即IgG和IgE中均观察到。最后,抗Ab2 T细胞与第一代独特型特异性细胞(抗Ab1细胞)的协同作用可进一步放大对抗体反应的辅助效应。与抗原特异性Th细胞一起,独特型特异性T细胞可能因其特异性和功能特性,在免疫反应的诱导中,更重要的是在免疫反应的维持中发挥主要作用。

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