Schmucker D L, Heyworth M F, Owen R L, Daniels C K
Cell Biology & Aging Section, Department of Veterans Affairs Medical Center, San Francisco, California 94121, USA.
Dig Dis Sci. 1996 Jun;41(6):1183-93. doi: 10.1007/BF02088236.
There is considerable evidence that the mucosal or secretory immune response in the gastrointestinal tract is compromised by aging. The generation of a mucosal immune response is an extremely complex process that involves antigenic stimulation of a specific subpopulation of immunologically competent cells in the Peyer's patches, differentiation and migration of these cells to the small intestinal lamina propria, initiation and regulation of local antibody production in the intestinal wall, and mucosal epithelial cell receptor-mediated transport of antibodies to the intestinal lumen. Available data suggest that gastrointestinal mucosal immunosenescence reflects deficits in: (1) the differentiation and/or migration (homing) of immunoglobulin A immunoblasts to the intestinal lamina propria, and (2) the initiation and/or regulation of local antibody production. The significant age-related increases in the incidence and severity of gastrointestinal infectious diseases, coupled with the potential for immunopharmacologic manipulation of the mucosal immune compartment, substantiate the merit of studies designed to resolve the etiology of mucosal immunodeficiency in the elderly.
有大量证据表明,胃肠道的黏膜或分泌性免疫反应会因衰老而受损。黏膜免疫反应的产生是一个极其复杂的过程,涉及对派尔集合淋巴结中特定免疫活性细胞亚群的抗原刺激、这些细胞向小肠固有层的分化和迁移、肠壁局部抗体产生的启动和调节,以及黏膜上皮细胞受体介导的抗体向肠腔的转运。现有数据表明,胃肠道黏膜免疫衰老反映在以下方面的缺陷:(1)免疫球蛋白A免疫母细胞向小肠固有层的分化和/或迁移(归巢),以及(2)局部抗体产生的启动和/或调节。胃肠道传染病的发病率和严重程度随年龄增长显著增加,再加上对黏膜免疫区室进行免疫药理学操纵的可能性,证实了旨在解决老年人黏膜免疫缺陷病因的研究的价值。