Isolated lymphoid follicle formation is inducible and dependent upon lymphotoxin-sufficient B lymphocytes, lymphotoxin β receptor, and TNF receptor I function
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作者:
Lorenz, RG
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机构:Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
Lorenz, RG
Chaplin, DD
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机构:Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
Chaplin, DD
McDonald, KG
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机构:Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
McDonald, KG
McDonough, JS
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机构:Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
McDonough, JS
Newderry, RD
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机构:Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
Newderry, RD
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[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[3] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
gastrointestinal mucosa contains a complex network of lymphoid compartments that have evolved to efficiently protect the host from invading pathogens.. Recently, an additional lymphoid structure resembling Peyer's patches (PP) in composition and architecture has been identified in the murine small intestine, the isolated lymphoid follicle (ILF). In this study we examine the nature and factors required for ILF formation. We observed a spectrum of structures fitting the previous descriptions of ILFs, ranging from clusters of B220(+) cells (which we have termed immature ILFs) to well-organized lymphoid nodules (which we have termed mature ILFs). Here we demonstrate that that similar to PP formation, ILF formation requires lymphotoxin (LT)- and LTbeta receptor-dependent events. However unlike PP formation, the LT- and LTbeta receptor-dependent events required for ILF formation can occur in adulthood and require LT-sufficient B lymphocytes. We demonstrate that mature ILF formation occurs in response to lumenal stimuli, including normal bacterial flora, and requires TNF receptor I function. These findings suggest that ILFs are organized intestinal lymphoid structures whose formation can be induced and whose mass can be expanded in response to mucosal challenges.