Pascual D W, Kiyono H, McGhee J R
Department of Oral Biology, University of Alabama, Birmingham Medical Center 35294.
Immunomethods. 1994 Aug;5(1):56-72. doi: 10.1006/immu.1994.1038.
A number of anatomical studies have demonstrated the presence of peptidergic nerve fibers infiltrating mucosal lymphoid tissues. The exact mechanisms of how neuropeptides are released to affect these lymphoid sites are unclear, but radiolabeled binding studies have shown that mucosal leukocytes bear a number of neuropeptide receptors on their cell surfaces capable of responding to neural signals. The presence of neuropeptide-containing fibers and the ability to receive neural signals suggest that mucosal lymphocytes can be influenced by neurogenic mediators. The objectives set forth in this review are to provide what is currently known about the ability of substance P and vasoactive intestinal peptide to promote mucosal IgA responses in the gastrointestinal tract via Th2 mechanisms and to discuss how these neuropeptides contribute to the exacerbation of the inflammatory diseases of the gastrointestinal tract. We describe how immune responses develop in the gastrointestinal immune system and emphasize how neuropeptides may influence the differentiation of lymphocytes in mucosal inductive tissues and their subsequent expression in mucosal effector sites. Finally, we discuss new techniques developed by the Mucosal Immunization Research Group that have enabled the study of mucosal immune responses.
多项解剖学研究已证实,肽能神经纤维会浸润黏膜淋巴组织。目前尚不清楚神经肽是如何释放以影响这些淋巴部位的确切机制,但放射性标记结合研究表明,黏膜白细胞在其细胞表面带有多种能够对神经信号作出反应的神经肽受体。含神经肽纤维的存在以及接收神经信号的能力表明,黏膜淋巴细胞可能会受到神经源性介质的影响。本综述提出的目标是提供目前已知的关于P物质和血管活性肠肽通过Th2机制促进胃肠道黏膜IgA反应的能力的信息,并讨论这些神经肽如何导致胃肠道炎症性疾病的加重。我们描述了胃肠道免疫系统中免疫反应是如何发展的,并强调神经肽可能如何影响黏膜诱导组织中淋巴细胞的分化及其在黏膜效应部位的后续表达。最后,我们讨论了黏膜免疫研究小组开发的新技术,这些技术使黏膜免疫反应的研究成为可能。