Richman L K, Graeff A S, Yarchoan R, Strober W
J Immunol. 1981 Jun;126(6):2079-83.
The effects of feeding the dietary protein antigen, ovalbumin (OVA), on OVA-specific IgG and IgA immune responses involving Peyer's patches (PP) and mesenteric lymph nodes (MLN) were examined. Mice were administered soluble OVA by gastric intubation. One to 3 days later, PP, MLN, or spleen cells from these donor mice were adoptively transferred into normal syngeneic recipients. After two subsequent immunizations, spleens from the recipient mice were assayed for IgA and IgG anti-OVA plaque-forming cell (PFC) responses. None of the tissues from normal (unfed) mice had the inherent ability to alter recipients' IgG or IgA PFC responses. Within 1 day of OVA feeding, however, cells were generated in the PP that could augment recipients' IgA anti-OVA PFC responses and suppress IgG PFC responses. Three days after OVA feeding, these cells were present in MLN as well, and whereas the IgG suppressor cell also appeared to migrate to spleen, the IgA helper cell did not. The cells mediating antigen-specific IgG suppression and IgA help were both T cells but could be distinguished by surface phenotype. We therefore conclude that protein feeding induces differential, isotype-specific immunoregulation in gut-associated lymphoid tissues, part of which is mediated by an antigen-specific IgA helper T cell.
研究了喂食膳食蛋白抗原卵清蛋白(OVA)对涉及派尔集合淋巴结(PP)和肠系膜淋巴结(MLN)的OVA特异性IgG和IgA免疫反应的影响。通过胃插管给小鼠施用可溶性OVA。1至3天后,将来自这些供体小鼠的PP、MLN或脾细胞过继转移到同基因正常受体中。在随后进行两次免疫后,检测受体小鼠脾脏中IgA和IgG抗OVA空斑形成细胞(PFC)反应。正常(未喂食)小鼠的任何组织都没有改变受体IgG或IgA PFC反应的内在能力。然而,在喂食OVA的1天内,PP中产生了能够增强受体IgA抗OVA PFC反应并抑制IgG PFC反应的细胞。喂食OVA 3天后,这些细胞也出现在MLN中,虽然IgG抑制细胞似乎也迁移到了脾脏,但IgA辅助细胞没有。介导抗原特异性IgG抑制和IgA辅助的细胞均为T细胞,但可通过表面表型加以区分。因此,我们得出结论,喂食蛋白质可在肠道相关淋巴组织中诱导差异性、同种型特异性免疫调节,其中部分调节由抗原特异性IgA辅助性T细胞介导。