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源自T细胞杂交瘤的单克隆抗原特异性增强因子不同链上IgT-C和I-A亚区域编码决定簇的存在。

Presence of IgT-C and I-A subregion-encoded determinants on distinct chains of monoclonal antigen-specific augmenting factor derived from a T cell hybridoma.

作者信息

Nakajima P B, Ochi A, Owen F L, Tada T

出版信息

J Exp Med. 1983 Jun 1;157(6):2110-20. doi: 10.1084/jem.157.6.2110.

Abstract

Monoclonal antibodies specific for mouse T cell alloantigens, Tindd and Tsud, linked to the Igh-1 locus on chromosome 12, were used to directly define the antigen-binding molecule produced by a cloned hybridoma. The T cell hybridoma, FL10, was established from antigen-binding T cells of A/J mice. FL10 produces an antigen-specific augmenting T cell factor (TaF) that bears a unique I region-controlled determinant (I-A) and has antigen-binding capacity. The Tindd, but not the Tsud, determinant was detected on the surface of FL10. The presence of both Tindd and I-A subregion-controlled determinants on FL10-derived TaF was directly demonstrated by the adsorption of TaF with immunoadsorbents prepared with monoclonal antibodies. The Igh-1-linked T cell alloantigen, Tsud, was not found on TaF. Further experiments indicated that Tindd is present on the antigen-binding polypeptide chain and not on the second chain bearing the I-A determinant. Despite the presence of the Tindd determinant on hybridoma-derived TaF, augmentation induced by TaF was restricted by the H-2 type of the responding mice and not by the Igh-1 allotype.

摘要

针对与12号染色体上Igh-1基因座相连的小鼠T细胞同种异体抗原Tindd和Tsud的单克隆抗体,被用于直接鉴定由克隆杂交瘤产生的抗原结合分子。T细胞杂交瘤FL10是从A/J小鼠的抗原结合T细胞中建立的。FL10产生一种抗原特异性增强T细胞因子(TaF),它带有一个独特的I区控制决定簇(I-A)并且具有抗原结合能力。在FL10的表面检测到了Tindd决定簇,但未检测到Tsud决定簇。通过用单克隆抗体制备的免疫吸附剂吸附TaF,直接证明了FL10衍生的TaF上同时存在Tindd和I-A亚区控制的决定簇。在TaF上未发现与Igh-1相连的T细胞同种异体抗原Tsud。进一步的实验表明,Tindd存在于抗原结合多肽链上,而不存在于带有I-A决定簇的第二条链上。尽管杂交瘤衍生的TaF上存在Tindd决定簇,但TaF诱导的增强作用受应答小鼠的H-2类型限制,而不受Igh-1同种异型的限制。

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