Feldmann M, Kontiainen S
Mol Cell Biochem. 1980 May 7;30(3):177-93. doi: 10.1007/BF00230172.
Antigen specific helper and suppressor factors have a similar structure, with two major sections, a 'variable region', determining antigen specificity which is likely to be controlled by Immunoglobulin VH genes, with which it shares idiotype and framework determinants. Specific factors also have a 'constant region' which does not vary between strains and minimally between species or with the antigenic specificity of the factors, which are defined by rabbit anti-helper or anti-suppressor antisera. This region determines the biological function of the molecule. Anti-Ia antisera react with factors, but the nature and function of Ia molecules on T cell factors is still unclear. The model of specific factor structure, with C and V regions resembles that of immunoglobulin, and it is thus possible that the C region of factors, like the V region is Ig linked. Because there are multiple T cells, helping and suppressing antibody responses specifically, it seems improbable that all of these cells could interact directly with rare antigen-specific B cells. Thus we propose that macrophage presenting cells are the key to the integration of signals for immune induction and regulation for T and B cells. Since Ir genes have been identified in the macrophage presenting cells interacting with both T and B cells, this suggests that macrophage Ia antigens are of importance in the integration of triggering signals for the lymphoid pool.
抗原特异性辅助因子和抑制因子具有相似的结构,有两个主要部分,一个“可变区”,决定抗原特异性,这可能由免疫球蛋白VH基因控制,它与免疫球蛋白共享独特型和框架决定簇。特异性因子还有一个“恒定区”,在不同品系间无变化,在不同物种间或因子的抗原特异性间变化最小,这些由兔抗辅助或抗抑制抗血清定义。该区域决定分子的生物学功能。抗Ia抗血清与因子发生反应,但T细胞因子上Ia分子的性质和功能仍不清楚。具有C区和V区的特异性因子结构模型类似于免疫球蛋白,因此因子的C区可能像V区一样与Ig相关。因为有多种T细胞特异性地辅助和抑制抗体反应,所有这些细胞似乎不太可能直接与罕见的抗原特异性B细胞相互作用。因此我们提出,巨噬细胞呈递细胞是T细胞和B细胞免疫诱导和调节信号整合的关键。由于在与T细胞和B细胞相互作用的巨噬细胞呈递细胞中已鉴定出Ir基因,这表明巨噬细胞Ia抗原在淋巴池触发信号的整合中很重要。