过继性细胞移植
白细胞介素2受体
免疫学
体外
败血症
医学
FOXP3型
肿瘤坏死因子α
生物
T细胞
免疫系统
生物化学
作者
Josef G. Heuer,Tonghai Zhang,Jingyong Zhao,Chunjin Ding,Martin S. Cramer,Kathy L. Justen,Steven Vonderfecht,Songqing Na
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2005-06-01
卷期号:174 (11): 7141-7146
被引量:121
标识
DOI:10.4049/jimmunol.174.11.7141
摘要
Abstract Regulatory CD4+CD25+ T cells (Tregs) suppress autoimmune and inflammatory diseases through mechanisms that are only partly understood. Previous studies suggest that Tregs can suppress bacterially triggered intestinal inflammation and respond to LPS through TLRs with enhanced suppressive activity. In this study, we have used murine cecal ligation and puncture as a model of polymicrobial sepsis to explore the effects of adoptive transfer of Tregs on septic outcome. Adoptive transfer of in vitro-stimulated Tregs in both prevention and therapeutic modes significantly improved survival of cecal ligation and puncture mice. Furthermore, the effect was dependent on both the number of Tregs adoptively transferred and the presence of host T cells. Animals that received stimulated Tregs had significantly increased peritoneal mast cells and peritoneal TNF-α production. More importantly, adoptive transfer of in vitro-stimulated Tregs significantly improved bacterial clearance, which resulted in improved survival. Our results suggest a novel role for Tregs in sepsis.
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