Taniguchi M, Hayakawa K, Tada T
J Immunol. 1976 Feb;116(2):542-8.
An antigen-specific suppressive T cell factor, which was extracted from carrier-primed T cells, was further characterized in an in vitro secondary antibody response. The factor was capable of suppressing secondary IgG antibody response of primed spleen cells when it was added to the culture together with relevant antigen. The suppressive T cell factor was not released from primed T cells by a short-term culture with antigen, but was kept bound to the membrane of the residual cultured cells, only the physical disruption of which can release the T cell factor. The target of the suppressive T cell factor was determined as being the helper T cell, since the factor did not exert any effect in the absence of the helper T cell with identical specificity to that of the factor. The suppressive activity was completely absorbed with alloantisera specific for products of the I region of H-2 complex, although various anti-immunoglobulin antisera failed to do so. Close analysis of the specificity of alloantisera capable of absorbing the suppressor molecule indicated that the suppressive T cell factor may, in fact, be an I region gene product probably coded for by genes in I-A and/or I-B (including I-E) subregions.
从载体致敏的T细胞中提取出一种抗原特异性抑制性T细胞因子,并在体外二次抗体应答中对其进行了进一步表征。当该因子与相关抗原一起添加到培养物中时,它能够抑制致敏脾细胞的二次IgG抗体应答。通过与抗原进行短期培养,抑制性T细胞因子不会从致敏T细胞中释放出来,而是与残留培养细胞的膜结合,只有通过物理破坏细胞膜才能释放出T细胞因子。抑制性T细胞因子的作用靶点被确定为辅助性T细胞,因为在没有与该因子具有相同特异性的辅助性T细胞的情况下,该因子不会发挥任何作用。抑制活性完全被针对H-2复合体I区产物的同种抗血清所吸收,尽管各种抗免疫球蛋白抗血清未能做到这一点。对能够吸收抑制分子的同种抗血清的特异性进行仔细分析表明,抑制性T细胞因子实际上可能是一种I区基因产物,可能由I-A和/或I-B(包括I-E)亚区的基因编码。