Germ-free mice do not develop ankylosing enthesopathy, a spontaneous joint disease

被引:55
作者
Reháková, Z [1 ]
Capková, J
Stepánková, R
Sinkora, J
Louzecká, A
Ivanyi, P
Weinreich, S
机构
[1] Acad Sci Czech Republ, Dept Immunol & Gnotobiol, Inst Microbiol, Novy Hradek 54922, Czech Republic
[2] Acad Sci Czech Republ, Inst Mol Genet, Prague, Czech Republic
[3] Inst Clin & Expt Med, Dept Immunogenet, Prague, Czech Republic
[4] Cent Lab Blood Transfus Serv, Dept Immunobiol, Amsterdam, Netherlands
关键词
spondyloarthropathies; animal model; germ-free; gut microflora; autoimmunity;
D O I
10.1016/S0198-8859(00)00122-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ankylosing enthesopathy (ANKENT) is a naturally occurring joint disease in mice with numerous parallels to human ankylosing spondylitis (AS). Similarities be tween AS and ANKENT include not only affected tissue (joint entheses) but also association of the disease with genetic background, including MHC genes, gender, and age. Young males with the C57B1/10 background have been described to suffer from ANKENT and, among H-2 congenic strains, high frequency of afflicted joints has been recorded in B10.BR (H-2(k)) males. Interestingly, the incidence of ANKENT is higher in conventional (CV) males that in their specific-pathogen-free (SPF) counterparts. The latter finding suggests that microbes could play a rule as an ANKENT-triggering agent. To further examine this hypothesis we have established a germ-free (GF) colony of B10.BR mice and observed ANKENT incidence in both GF males and their conventionalized (ex-GF) male littermates; 20% of ex-GF males developed ANKENT before 1 year of age. In contrast, no joint disease was observed under GF conditions (p < 0.0001). Our results show that live microflora is required in ANKENT pathogenesis. (C) American Society for Histocompatibility and Immunogenetics, 2000. Published by Elsevier Science Inc.
引用
收藏
页码:555 / 558
页数:4
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