Differing Influences of Virus Burden and Immune Activation on Disease Severity in Secondary Dengue‐3 Virus Infections

Daniel H. Libraty(University of Massachusetts Chan Medical School), Timothy P. Endy(Armed Forces Research Institute of Medical Science), Huo‐Shu H. Houng(Walter Reed Army Institute of Research), Sharone Green(University of Massachusetts Chan Medical School), Siripen Kalayanarooj(Queen Sirikit National Institute of Child Health), Saroj Suntayakorn(Kamphaeng Phet Rajabhat University), Wanya Chansiriwongs(Queen Sirikit National Institute of Child Health), David W. Vaughn(Walter Reed Army Institute of Research), Ananda Nisalak(Armed Forces Research Institute of Medical Science), Francis A. Ennis(University of Massachusetts Chan Medical School), Alan L. Rothman(University of Massachusetts Chan Medical School)
The Journal of Infectious Diseases
May 1, 2002
Cited by 488Open Access
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Abstract

Dengue hemorrhagic fever (DHF), the most severe form of illness following infection with a dengue virus, is characterized by plasma leakage, thrombocytopenia, and hepatic inflammation. The interrelationships among virus burden, immune activation, and development of DHF were examined in 54 children with secondary dengue-3 virus infections participating in a prospective, hospital-based study. DHF was associated with higher mean plasma viremia early in illness and earlier peak plasma interferon-gamma levels. Maximum plasma viremia levels correlated with the degree of plasma leakage and thrombocytopenia. Maximum plasma levels of interleukin (IL)-10 and soluble tumor necrosis factor receptor-II correlated with the degree of thrombocytopenia, independently of viremia levels. Hepatic transaminase elevation correlated with plasma soluble IL-2 receptor levels and not with viremia levels. Quantitative differences in virus burden and host immune responses, and the timing of type 1 cytokine responses, have differing influences on the severity of disease manifestations during secondary dengue-3 virus infections.


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