Lamm M E
Institute of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106.
Am J Kidney Dis. 1988 Nov;12(5):384-7. doi: 10.1016/s0272-6386(88)80030-1.
This report reviews the immunophysiology of the mucosal immune system, the principal antibody of which is a special form of IgA, termed secretory IgA. This IgA is produced locally by mucosal plasma cells that are descended from precursors initially stimulated in organized, mucosal lymphoid organs designed for antigen sampling. After the initial triggering, the precursor cells pass via regional lymph nodes, lymph, and blood to disseminate widely among mucosal sites. After secretion from a local plasma cell, IgA binds to an epithelial cell surface receptor and the complex passes through the epithelial cell into the secretions where it serves as a nonphlogistic immunologic barrier to inhibit uptake of antigens. The production of IgA is facilitated by particular regulatory T cells. At the same time, the synthesis of other classes of antibody, such as the phlogistic IgG, is dampened. This differential regulation of individual antibody classes after exposure to mucosal antigen plus the interrelatedness of the various mucous membranes of the body have important implications for host defense, pathogenesis of a variety of diseases including IgA nephropathy, and strategies of immunization.
本报告回顾了黏膜免疫系统的免疫生理学,其主要抗体是一种特殊形式的IgA,称为分泌型IgA。这种IgA由黏膜浆细胞在局部产生,这些浆细胞源自最初在专门用于抗原采样的有组织的黏膜淋巴器官中受到刺激的前体细胞。在最初被触发后,前体细胞通过区域淋巴结、淋巴和血液在黏膜部位广泛传播。从局部浆细胞分泌后,IgA与上皮细胞表面受体结合,复合物穿过上皮细胞进入分泌物中,在那里它作为一种非炎性免疫屏障抑制抗原的摄取。特定的调节性T细胞促进IgA的产生。与此同时,其他类别的抗体,如炎性IgG的合成则受到抑制。接触黏膜抗原后对各个抗体类别的这种差异调节以及身体各种黏膜的相互关联性对宿主防御、包括IgA肾病在内的多种疾病的发病机制以及免疫策略都具有重要意义。