Briese V
Zentralbl Gynakol. 1986;108(21):1282-8.
Mucosal immunity of the female genital tract is a part of the "Common mucosal immunity". It is possible to induce local antibodies in the female genital tract by means of oral immunization. From these investigations new perspectives in terms of immunoprophylaxis against bacterial, viral an parasitic infections come into consideration for clinical use. In the case of bacterial infections IgA blocks the attachment of pathogens to relevant mucosal tissues and cells. Predominant among the immune mechanisms is the occurrence of secretory antibodies in the fluids that bath mucosal membranes. Secretory IgA (S-IgA) is an 11S molecule (MW 390,000) consisting of two IgA monomers covalently bonded by joining chain (J chain) and complexed to one molecule of SC.S-IgA ist the main immunoglobulin of mucosal surface. A medically important group of bacterial pathogens produce IgA1 protease cleaving only IgA1 proteins. S-IgA is resistant to protease hydrolysis. The secretory component (SC) is an epithelial cell receptor for the transport of IgA dimers, polymers and IgM polymers. Systemic suppression after oral antigen application has been demonstrated with a variety of thymic-dependent antigens, including heterologous erythrocytes, haptens, and various soluble proteins. Tolerance is mediated by antigen specific T suppressor cells (Ts). Suppressor cells first appear in the gut associated lymphoid tissue and subsequently migrate to systemic sites. At present immunoglobulin estimations in secretions are of clinical importance regarding supporting diagnostic tool of mucosal infections.(ABSTRACT TRUNCATED AT 250 WORDS)
女性生殖道的黏膜免疫是“共同黏膜免疫”的一部分。通过口服免疫可在女性生殖道诱导产生局部抗体。基于这些研究,在针对细菌、病毒和寄生虫感染的免疫预防方面出现了新的临床应用视角。在细菌感染的情况下,IgA可阻止病原体附着于相关黏膜组织和细胞。免疫机制中主要的是在覆盖黏膜的体液中出现分泌性抗体。分泌型IgA(S-IgA)是一种11S分子(分子量390,000),由两条通过连接链(J链)共价结合的IgA单体组成,并与一个分泌成分(SC)分子结合。S-IgA是黏膜表面的主要免疫球蛋白。一类具有医学重要性的细菌病原体可产生仅裂解IgA1蛋白的IgA1蛋白酶。S-IgA对蛋白酶水解具有抗性。分泌成分(SC)是IgA二聚体、多聚体及IgM多聚体转运的上皮细胞受体。口服抗原后已证实对多种胸腺依赖性抗原会出现全身抑制,包括异种红细胞、半抗原及各种可溶性蛋白。耐受性由抗原特异性T抑制细胞(Ts)介导。抑制细胞首先出现在肠道相关淋巴组织中,随后迁移至全身部位。目前,分泌物中的免疫球蛋白测定对于支持黏膜感染的诊断工具具有临床重要性。(摘要截选至250词)