造血
生物
基孔肯雅
病毒
免疫系统
病毒学
免疫学
干扰素
细胞生物学
干细胞
作者
Clémentine Schilte,Matthew R. Buckwalter,Melissa E. Laird,Michael Diamond,Olivier Schwartz,Matthew L. Albert
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2012-02-28
卷期号:188 (7): 2967-2971
被引量:88
标识
DOI:10.4049/jimmunol.1103185
摘要
The host response to Chikungunya virus is dependent on the direct action of type I IFN on infected nonhematopoietic cells. Prior studies have demonstrated that multiple host sensors coordinate an antiviral response; however, the tissue source(s) and signaling pathways for IFN production remain unknown. In this study, we demonstrate that IRF-3 and IRF-7 are functionally redundant, but lack of both factors results in lethal infection in adult mice. Reciprocal bone marrow chimeras indicated that IRF-3 or IRF-7 expression in either hematopoietic or nonhemotopoietic cell compartments was capable of inducing an antiviral response. Interestingly, redundancy of IRF-3 and IRF-7 was age dependent, as neonatal animals lacking either factor succumbed to infection. We further demonstrate that IPS-1 is essential in nonhematopoietic cells and preferentially required during early life. These results highlight the interplay between nonimmune and immune cells during Chikungunya virus infection and suggest an important role for nonhematopoietic cells as a critical source of IFN-α/β.
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