Flood P M, Lowy A, Tominaga A, Chue B, Greene M I, Gershon R K
J Exp Med. 1983 Dec 1;158(6):1938-47. doi: 10.1084/jem.158.6.1938.
Immunized Ly-1 T cells secrete an antigen-specific molecule that will induce Ly-2+ T cells to express suppressive activity. In two separate systems, factors that suppress the primary anti-sheep erythrocyte (SE) plaque-forming cell response of spleen cells in vitro (Ly-1 TsiF) or the contact sensitivity of azobenzenearsonate (ABA)-TsF1 consist of two macromolecules, one which binds antigen and is IJ-, the other which is I-J+ and does not bind antigen. Both of these chains are required for the factor's biological activity. These factors show a genetic restriction in their ability to induce suppression that is linked to the variable region of the Ig heavy chain gene complex (Igh-V). The I-J+ chain from the ABA-specific TsF1 could replace the I-J+ chain needed by the SE-specific Ly-1 TsiF for biological activity. Mixtures of ABA-binding chain with I-J+ material obtained from the SE-specific Ly-1 TsiF had no effect on the primary anti-SE response in vitro. In mixtures of SE antigen-binding chain from Ly-1 TsiF and I-J+ material from the ABA-specific TsF1, it is the I-J+ molecule that determined the factor's Igh-V restriction. Thus, the antigen-combining site of the factor determined the antigen specificity of this factor but is irrelevant to its Igh-V-linked genetic restrictions. The implications of these results for the idiotype network hypothesis are discussed.
免疫的Ly-1 T细胞分泌一种抗原特异性分子,该分子可诱导Ly-2⁺ T细胞表达抑制活性。在两个独立的系统中,体外抑制脾细胞对绵羊红细胞(SE)的原发性噬斑形成细胞反应的因子(Ly-1 TsiF)或偶氮苯胂酸(ABA)-TsF1的接触敏感性由两种大分子组成,一种结合抗原且为I-J⁻,另一种为I-J⁺且不结合抗原。这两条链对于该因子的生物学活性都是必需的。这些因子在诱导抑制的能力上表现出与免疫球蛋白重链基因复合体(Igh-V)可变区相关的遗传限制。来自ABA特异性TsF1的I-J⁺链可以替代SE特异性Ly-1 TsiF生物学活性所需的I-J⁺链。ABA结合链与从SE特异性Ly-1 TsiF获得的I-J⁺物质的混合物对体外原发性抗SE反应没有影响。在来自Ly-1 TsiF的SE抗原结合链与来自ABA特异性TsF1的I-J⁺物质的混合物中,决定因子Igh-V限制的是I-J⁺分子。因此,该因子的抗原结合位点决定了该因子的抗原特异性,但与其Igh-V连锁的遗传限制无关。讨论了这些结果对独特型网络假说的意义。