An animal model of autoimmune emphysema

被引:129
作者
Taraseviciene-Stewart, L
Scerbavicius, R
Chloe, KH
Moore, M
Sullivan, A
Nicolls, MR
Fontenot, AP
Tuder, RM
Voelkel, NF
机构
[1] Univ Colorado, Hlth Sci Ctr, Dept Med, Div Pulm Sci, Denver, CO 80262 USA
[2] Univ Colorado, Hlth Sci Ctr, Dept Immunol, Div Pulm Sci, Denver, CO 80262 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Div Cardiopulm Pathol, Baltimore, MD 21205 USA
关键词
apoptosis; autoimmunity; CD4+T cells; emphysema; endothelial cells;
D O I
10.1164/rccm.200409-1275OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Although cigarette smoking is implicated in the pathogenesis of emphysema, the precise mechanisms of chronic progressive alveolar septal destruction are not well understood. We show, in a novel animal model, that immunocompetent, but not athymic, nude rats injected intraperitoneally with xenogeneic endothelial cells (ECs) produce antibodies against ECs and develop emphysema. Immunization with ECs also leads to alveolar septal cell apoptosis and activation of matrix metalloproteases MMP-9 and MMP-2. Anti-EC antibodies cause EC apoptosis in vitro and emphysema in passively immunized mice. Moreover, immunization also causes accumulation of CD4+ T cells in the lung. Adoptive transfer of pathogenic, spleen-derived CD4+ cells into naive immunocompetent animal also results in emphysema. This study shows for the first time that humoral- and CD4+ cell-dependent mechanisms are sufficient to trigger the development of emphysema, suggesting that alveolar septal cell destruction might result from immune mechanisms.
引用
收藏
页码:734 / 742
页数:9
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