Kang Hyung-Sik, Chin Robert K, Wang Yang, Yu Ping, Wang Jun, Newell Kenneth A, Fu Yang-Xin
Department of Pathology and Committee on Immunology, The University of Chicago, 5841 S. Maryland, Chicago, IL 60637, USA.
Nat Immunol. 2002 Jun;3(6):576-82. doi: 10.1038/ni795. Epub 2002 May 13.
Peyer's patches (PPs) and/or mesenteric lymph nodes (MLNs) are thought to be essential for immunoglobulin A (IgA) production. We found that the severe IgA deficiency in lymphotoxin-deficient (LT(-/-)) mice could be fully reversed by reconstitution with LT-expressing bone marrow, despite the absence of both LNs and PPs. The number of IgA precursors from LT(-/-) mice was not reduced, and they were able to migrate into the lamina propria (LP) of wild-type mice but not of LTbetaR(-/-) mice. Consistently, lymphoid tissue chemokines and adhesion molecules were reduced within the LP of LTalpha(-/-) and LTbetaR(-/-) mice. IgA deficiency in LTalpha(-/-) mice was reversed by the transplantation of a segment of RAG-1 (recombination-activating gene 1) deficient intestine, which confirmed the dispensability of the MLNs and PPs and the sufficiency of the LT-mediated gut microenvironment for IgA production.
派尔集合淋巴结(PPs)和/或肠系膜淋巴结(MLNs)被认为是产生免疫球蛋白A(IgA)所必需的。我们发现,尽管缺乏淋巴结和派尔集合淋巴结,但用表达淋巴毒素的骨髓进行重建可完全逆转淋巴毒素缺陷(LT(-/-))小鼠的严重IgA缺乏。LT(-/-)小鼠的IgA前体细胞数量并未减少,它们能够迁移到野生型小鼠的固有层(LP),但不能迁移到LTβR(-/-)小鼠的固有层。一致地,LTα(-/-)和LTβR(-/-)小鼠固有层内的淋巴组织趋化因子和黏附分子减少。通过移植一段RAG-1(重组激活基因1)缺陷的肠道,逆转了LTα(-/-)小鼠的IgA缺乏,这证实了肠系膜淋巴结和派尔集合淋巴结并非必需,以及LT介导的肠道微环境对于IgA产生是足够的。