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主要组织相容性复合体(MHC)和辅助性T细胞独特型的免疫球蛋白基因控制的基础。

The basis for major histocompatibility complex (MHC) and immunoglobulin gene control of helper T cell idiotopes.

作者信息

Martinez-A C, Pereira P, de la Hera A, Bandeira A, Marquez C, Coutinho A

出版信息

Eur J Immunol. 1986 Apr;16(4):417-22. doi: 10.1002/eji.1830160418.

Abstract

BALB/c helper T cells, prepared against 2,4,6-trinitrophenyl (TNP)-derivatized syngeneic spleen cells, fail to recognize other hapten modifications [(4-hydroxy-3-nitrophenyl)acetyl, fluorescein isothiocyanate] of syngeneic cells, as well as TNP-derivatized cells from major histocompatibility complex-congenic donors. T helper cell interactions with "presenting" cells and "target" B lymphocytes are inhibited by monoclonal antibodies directed either to the hapten or to I-A molecules on target cells. Helper activity is also inhibited by monoclonal anti-idiotypic antibodies directed to an idiotope expressed by the TNP-binding myeloma protein MOPC460, but not by soluble TNP-protein conjugates. The study of congenic mouse strains revealed that while the fine specificity of TNP recognition and the quantitative levels of M 460 idiotope expression are I-A linked, the expression of the M 460 idiotope by helper cells is controlled by IgCh-linked genes. Absence of anti-idiotope inhibition of helper cells prepared in anti-mu-suppressed mice suggests, however, that immunoglobulin idiotype expression by T cells results from network interactions selecting available lymphocyte repertoires which operate before antigenic stimulation.

摘要

针对2,4,6-三硝基苯基(TNP)衍生的同基因脾细胞制备的BALB/c辅助性T细胞,无法识别同基因细胞的其他半抗原修饰([4-羟基-3-硝基苯基]乙酰基、异硫氰酸荧光素),以及来自主要组织相容性复合体同基因供体的TNP衍生细胞。辅助性T细胞与“呈递”细胞和“靶”B淋巴细胞的相互作用受到针对半抗原或靶细胞上I-A分子的单克隆抗体的抑制。辅助活性也受到针对TNP结合骨髓瘤蛋白MOPC460表达的独特型表位的单克隆抗独特型抗体的抑制,但不受可溶性TNP-蛋白质缀合物的抑制。对同基因小鼠品系的研究表明,虽然TNP识别的精细特异性和M 460独特型表位表达的定量水平与I-A相关,但辅助性细胞对M 460独特型表位的表达受IgCh连锁基因控制。然而,在抗μ抑制的小鼠中制备的辅助性细胞缺乏抗独特型抑制,这表明T细胞的免疫球蛋白独特型表达是由在抗原刺激之前选择可用淋巴细胞库的网络相互作用导致的。

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