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抗抗H-2单克隆抗体的抗独特型抗体。V. 体内抗独特型治疗诱导独特型特异性辅助性T细胞。

Antiidiotypes against anti-H-2 monoclonal antibodies. V. In vivo antiidiotype treatment induces idiotype-specific helper T cells.

作者信息

Auchincloss H, Bluestone J A, Sachs D H

出版信息

J Exp Med. 1983 Apr 1;157(4):1273-86. doi: 10.1084/jem.157.4.1273.

Abstract

Mice have been treated in vivo with xenogeneic antiidiotypes prepared against a murine monoclonal anti-H-2Kk antibody, 11-4.1. B cell immune responses have been found to be altered by such treatment as evidenced by a modification in the idiotypic repertoire of the humoral response to H-2 antigens. Transfer of purified T cells into nude mice before anti-idiotype treatment showed that T cells are involved in the induction of idiotope-bearing antibodies by xenogeneic antiidiotype. Studies using bone marrow chimeras indicate that the environment in which either T or B cells mature does not appear to alter VH region genetic control of induction of antiidiotype-induced molecules. By adoptive transfer studies, T cells from antiidiotype-treated mice were found capable of modifying the idiotypic repertoire of B cells subsequently exposed to antigen even when the T cells were obtained from antiidiotype-primed mice of inappropriate allotype. Although it still must be determined whether idiotypic or antiidiotypic T cells are involved in such B cell idiotype regulation, these results indicate that some T cell functions are altered by xenogeneic antiidiotypes prepared against B cell products and suggest that T cell immunity to major histocompatibility complex antigens may also be affected by such reagents.

摘要

已用针对鼠单克隆抗H-2Kk抗体11-4.1制备的异种抗独特型在体内处理小鼠。如对H-2抗原的体液应答的独特型库的改变所证明,已发现这种处理会改变B细胞免疫应答。在抗独特型处理前将纯化的T细胞转移到裸鼠中表明,T细胞参与异种抗独特型诱导携带独特位的抗体。使用骨髓嵌合体的研究表明,T细胞或B细胞成熟的环境似乎不会改变抗独特型诱导分子诱导的VH区基因控制。通过过继转移研究发现,来自抗独特型处理小鼠的T细胞能够改变随后暴露于抗原的B细胞的独特型库,即使T细胞是从不合适同种异型的抗独特型致敏小鼠中获得的。虽然仍必须确定独特型或抗独特型T细胞是否参与这种B细胞独特型调节,但这些结果表明,针对B细胞产物制备的异种抗独特型会改变一些T细胞功能,并表明针对主要组织相容性复合体抗原的T细胞免疫也可能受此类试剂影响。

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Induction and regulation of silent idiotype clones.沉默独特型克隆的诱导与调控。
Eur J Immunol. 1981 May;11(5):393-8. doi: 10.1002/eji.1830110509.

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