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一种抗原特异性、Ly-1 T抑制诱导因子的分子组成。一个分子结合抗原且为I-J-;另一个为I-J+,不结合抗原,并赋予与免疫球蛋白可变区相关的限制性。

Molecular composition of an antigen-specific, Ly-1 T suppressor inducer factor. One molecule binds antigen and is I-J-; another is I-J+, does not bind antigen, and imparts an Igh-variable region-linked restriction.

作者信息

Yamauchi K, Chao N, Murphy D B, Gershon R K

出版信息

J Exp Med. 1982 Mar 1;155(3):655-65. doi: 10.1084/jem.155.3.655.

Abstract

Immunized Ly-1+2-T cells (Ly-1 cells) make an antigen-specific soluble suppressor product (Lyl-1 TsiF) that will induce Ly-2+ cells to express suppressive activity but only if the Ly-2+ and the Ly-1 producer cell share genetic polymorphisms that are linked to the Igh locus and in particular that part where the Igh-V (or VH) is encoded. Ly-1 TsiF can be separated into entities, one binds antigen and does not express I-J determinants, and the other is I-J+ and does not bind antigen. Neither of these "subfactors" has biological activity, but a 50:50 mixture of them reconstitutes biological activity that expresses the antigen specificity of the antigen-binding molecule. Any of the three heterologous erythrocytes (antigens) studied can be used for immunization to produce the I-J+ nonantigen-binding factor, i.e., the I-J+ moiety makes no contribution to the factor's specificity. It does, however, determine the intact factor's Igh-V linked restriction. Thus, the antigen combining site of the factor is irrelevant to the factor's Igh-V restriction but crucial for its specificity. The I-J+ molecule does not bind antigen nor influence the factor's antigen specificity but expresses the Igh-V polymorphism (or anti-Igh-V polymorphism) that is required for the transmission of an inductive signal to the factor's Ly-2+ acceptor cell.

摘要

免疫的Ly-1⁺2⁻T细胞(Ly-1细胞)产生一种抗原特异性可溶性抑制产物(Lyl-1 TsiF),该产物会诱导Ly-2⁺细胞表达抑制活性,但前提是Ly-2⁺细胞和Ly-1产生细胞共享与Igh基因座相关的遗传多态性,特别是Igh-V(或VH)编码的部分。Ly-1 TsiF可分为两个部分,一个结合抗原且不表达I-J决定簇,另一个是I-J⁺且不结合抗原。这两种“亚因子”都没有生物学活性,但它们以50:50的混合物重构后具有生物学活性,且该活性表达了抗原结合分子的抗原特异性。所研究的三种异源红细胞(抗原)中的任何一种都可用于免疫以产生I-J⁺非抗原结合因子,即I-J⁺部分对因子的特异性没有贡献。然而,它决定了完整因子与Igh-V相关的限制。因此,因子的抗原结合位点与因子的Igh-V限制无关,但对其特异性至关重要。I-J⁺分子不结合抗原,也不影响因子的抗原特异性,但表达了将诱导信号传递给因子的Ly-2⁺受体细胞所需的Igh-V多态性(或抗Igh-V多态性)。

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