Evidence for an interferon-inducible gene, Ifi202, in the susceptibility to systemic lupus

被引:289
作者
Rozzo, SJ
Allard, JD
Choubey, D
Vyse, TJ
Izui, S
Peltz, G
Kotzin, BL [1 ]
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Med, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Denver, CO 80262 USA
[3] Roche Biosci, Palo Alto, CA 94304 USA
[4] Loyola Univ, Stritch Sch Med, Dept Radiat Oncol, Maywood, IL 60153 USA
[5] Ctr Med Univ Geneva, Dept Pathol, CH-1211 Geneva 4, Switzerland
[6] Natl Jewish Med & Res Ctr, Dept Med, Denver, CO 80206 USA
关键词
D O I
10.1016/S1074-7613(01)00196-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Nba2 locus is a major genetic contribution to disease susceptibility in the (NZB X NZW)F-1 mouse model of systemic lupus. We generated C57BL/6 mice congenic for this NZB locus, and these mice produced antinuclear autoantibodies characteristic of lupus. F-1 offspring of congenic and NZW mice developed high autoantibody levels and severe lupus nephritis similar to (NZB X NZW)F1 mice. Expression profiling with oligonucleotide microarrays revealed only two differentially expressed genes, interferon-inducible genes Ifi202 and Ifi203, in congenic versus control mice, and both were within the Nba2 interval. Quantitative PCR localized increased Ifi202 expression to splenic B cells and non-T/non-B cells. These results, together with analyses of promoter region polymorphisms, strain distribution of expression, and effects on cell proliferation and apoptosis, implicate Ifi202 as a candidate gene for lupus.
引用
收藏
页码:435 / 443
页数:9
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