Kawano Y, Noma T, Kou K, Yoshizawa I, Yata J
Department of Pediatrics, Saitama Medical School, Japan.
Immunology. 1995 Feb;84(2):278-84.
Peripheral blood mononuclear cells (PBMC) stimulated with pokeweed mitogen (PWM) produced increased IgG when cultured with interleukin-6 (IL-6). IgG subclass analysis showed that the presence of IL-6 during the last half of the culture period enhanced IgG1 and IgG4 production. Enhancement of IgG2 synthesis required the presence of IL-6 solely during the last half of the culture period, whereas enhancement paradoxically was blocked by its presence during the first half. The IgG3-enhancing effect of IL-6 was observed only when IL-6 was present throughout the culture period. The critical role of IL-6 was supported by the inhibition of IgG subclass synthesis by anti-IL-6 antibody. PBMC depleted of cells bearing surface IgG of a particular subclass did not synthesize that subclass. This non-responsiveness, which was not reversed even by an addition of IL-6, indicates that the main action of IL-6 is on the differentiation of committed B cells. In addition, IL-6 triggered T cells to produce significant helper activity. These results indicate that IL-6 enhances IgG subclass production differentially and that its critical role in IgG subclass synthesis is in part mediated by T cells, as well as by its direct action on B cells. These findings should be useful for analysing such immune disorders as IgG subclass deficiencies and autoimmune diseases.
用美洲商陆丝裂原(PWM)刺激的外周血单个核细胞(PBMC)与白细胞介素-6(IL-6)一起培养时产生的IgG增加。IgG亚类分析表明,在培养期的后半段存在IL-6可增强IgG1和IgG4的产生。IgG2合成的增强仅在培养期的后半段需要IL-6的存在,而矛盾的是,在前半段存在IL-6时增强作用被阻断。仅当在整个培养期都存在IL-6时,才观察到IL-6对IgG3的增强作用。抗IL-6抗体对IgG亚类合成的抑制支持了IL-6的关键作用。去除带有特定亚类表面IgG的细胞的PBMC不合成该亚类。这种无反应性,即使添加IL-6也不能逆转,表明IL-6的主要作用是对已定向的B细胞的分化。此外,IL-6触发T细胞产生显著的辅助活性。这些结果表明,IL-6以不同方式增强IgG亚类的产生,并且其在IgG亚类合成中的关键作用部分由T细胞介导,以及由其对B细胞的直接作用介导。这些发现对于分析诸如IgG亚类缺陷和自身免疫性疾病等免疫紊乱应该是有用的。