Active Infection of Human Blood Monocytes by Chikungunya Virus Triggers an Innate Immune Response

被引:220
作者
Her, Zhisheng [1 ,2 ]
Malleret, Benoit [1 ]
Chan, Monica [3 ]
Ong, Edward K. S. [1 ]
Wong, Siew-Cheng [1 ]
Kwek, Dyan J. C. [1 ]
Tolou, Hugues [5 ]
Lin, Raymond T. P. [3 ,4 ]
Tambyah, Paul Anantharajah [3 ]
Renia, Laurent [1 ]
Ng, Lisa F. P. [1 ,2 ]
机构
[1] Agcy Sci Technol & Res, Singapore Immunol Network, Singapore 138648, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117595, Singapore
[3] Natl Univ Hlth Syst, Dept Lab Med, Natl Univ Hosp, Singapore, Singapore
[4] Minist Hlth, Natl Publ Hlth Lab, Div Communicable Dis, Singapore, Singapore
[5] Inst Rech Biomed Armees, Inst Trop Med, Lab Trop Virol, Serv Sante Armees, Marseille, France
关键词
REUNION ISLAND; CELL-DEATH; T-CELLS; CD14; DIFFERENTIATION; RECEPTOR; EPIDEMIC; LIPOPOLYSACCHARIDE; REPLICATION; EXPRESSION;
D O I
10.4049/jimmunol.0904181
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Chikungunya virus (CHIKV) is an alphavirus that causes chronic and incapacitating arthralgia in humans. To date, interactions between the immune system and the different stages of the virus life cycle remain poorly defined. We demonstrated for the first time that CHIKV Ags could be detected in vivo in the monocytes of acutely infected patients. Using in vitro experimental systems, whole blood and purified monocytes, we confirmed that monocytes could be infected and virus growth could be sustained. CHIKV interactions with monocytes, and with other blood leukocytes, induced a robust and rapid innate immune response with the production of specific chemokines and cytokines. In particular, high levels of IFN-alpha were produced rapidly after CHIKV incubation with monocytes. The identification of monocytes during the early phase of CHIKV infection in vivo is significant as infected monocyte/macrophage cells have been detected in the synovial tissues of chronically CHIKV-infected patients, and these cells may behave as the vehicles for virus dissemination. This may explain the persistence of joint symptoms despite the short duration of viremia. Our results provide a better understanding on the basic mechanisms of infection and early antiviral immune responses and will help in the development of future effective control strategies. The Journal of Immunology, 2010, 184: 5903-5913.
引用
收藏
页码:5903 / 5913
页数:11
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