Proinflammatory cytokines and chemokines in humans with Japanese encephalitis

Background. Japanese encephalitis virus (JEV), the mosquito-borne flavivirus, annually causes an estimated 35,000-50,000 encephalitis cases and 10,000-15,000 deaths in Asia, and there is no antiviral treatment. The role played by the immune response in determining the outcome of human infection with...

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Main Authors: Peter M. Winter, Minh Dung Nguyen, Thi Loan Ha, Rachel Kneen, Bridget Wills, Thi Thu Le, Deborah House, Nicholas J. White, Jeremy J. Farrar, C. Anthony Hart, Tom Solomon
Other Authors: University of Liverpool
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/21506
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spelling th-mahidol.215062018-07-24T10:47:26Z Proinflammatory cytokines and chemokines in humans with Japanese encephalitis Peter M. Winter Minh Dung Nguyen Thi Loan Ha Rachel Kneen Bridget Wills Thi Thu Le Deborah House Nicholas J. White Jeremy J. Farrar C. Anthony Hart Tom Solomon University of Liverpool Hospital for Tropical Diseases Centre for Tropical Diseases Vietnam Mahidol University Medicine Background. Japanese encephalitis virus (JEV), the mosquito-borne flavivirus, annually causes an estimated 35,000-50,000 encephalitis cases and 10,000-15,000 deaths in Asia, and there is no antiviral treatment. The role played by the immune response in determining the outcome of human infection with JEV is poorly understood, although, in animal models of flavivirus encephalitis, unregulated proinflammatory cytokine responses can be detrimental. Methods. We studied the innate, cellular, and humoral immune responses in 118 patients infected with JEV, of whom 13 (11%) died. Results. Levels of interferon (IFN)-α, the proinflammatory cytokine interleukin (IL)-6, and the chemokine IL-8 were all higher in the cerebrospinal fluid (CSF) of the nonsurvivors than of the survivors (P = .04, P = .006, and P = .04, respectively), as were both the IL-6:IL-4 ratio in CSF (a marker of the balance of pro- and anti-inflammatory cytokines) and the level of the chemokine RANTES (regulated on activation, normally T cell expressed and secreted) in plasma (P = .03). In contrast, levels of immunoglobulin (Ig) M and IgG in CSF and of IgM in plasma were higher in the survivors (P = .035, P = .003, and P = .009, respectively). Levels of IFN-γ and nitric oxide did not vary with outcome. Conclusions. During JEV infection, elevated levels of proinflammatory cytokines and chemokines are associated with a poor outcome, but whether they are simply a correlate of severe disease or contribute to pathogenesis remains to be determined. 2018-07-24T03:47:26Z 2018-07-24T03:47:26Z 2004-11-01 Article Journal of Infectious Diseases. Vol.190, No.9 (2004), 1618-1626 10.1086/423328 00221899 2-s2.0-6944246228 https://repository.li.mahidol.ac.th/handle/123456789/21506 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=6944246228&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
Peter M. Winter
Minh Dung Nguyen
Thi Loan Ha
Rachel Kneen
Bridget Wills
Thi Thu Le
Deborah House
Nicholas J. White
Jeremy J. Farrar
C. Anthony Hart
Tom Solomon
Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
description Background. Japanese encephalitis virus (JEV), the mosquito-borne flavivirus, annually causes an estimated 35,000-50,000 encephalitis cases and 10,000-15,000 deaths in Asia, and there is no antiviral treatment. The role played by the immune response in determining the outcome of human infection with JEV is poorly understood, although, in animal models of flavivirus encephalitis, unregulated proinflammatory cytokine responses can be detrimental. Methods. We studied the innate, cellular, and humoral immune responses in 118 patients infected with JEV, of whom 13 (11%) died. Results. Levels of interferon (IFN)-α, the proinflammatory cytokine interleukin (IL)-6, and the chemokine IL-8 were all higher in the cerebrospinal fluid (CSF) of the nonsurvivors than of the survivors (P = .04, P = .006, and P = .04, respectively), as were both the IL-6:IL-4 ratio in CSF (a marker of the balance of pro- and anti-inflammatory cytokines) and the level of the chemokine RANTES (regulated on activation, normally T cell expressed and secreted) in plasma (P = .03). In contrast, levels of immunoglobulin (Ig) M and IgG in CSF and of IgM in plasma were higher in the survivors (P = .035, P = .003, and P = .009, respectively). Levels of IFN-γ and nitric oxide did not vary with outcome. Conclusions. During JEV infection, elevated levels of proinflammatory cytokines and chemokines are associated with a poor outcome, but whether they are simply a correlate of severe disease or contribute to pathogenesis remains to be determined.
author2 University of Liverpool
author_facet University of Liverpool
Peter M. Winter
Minh Dung Nguyen
Thi Loan Ha
Rachel Kneen
Bridget Wills
Thi Thu Le
Deborah House
Nicholas J. White
Jeremy J. Farrar
C. Anthony Hart
Tom Solomon
format Article
author Peter M. Winter
Minh Dung Nguyen
Thi Loan Ha
Rachel Kneen
Bridget Wills
Thi Thu Le
Deborah House
Nicholas J. White
Jeremy J. Farrar
C. Anthony Hart
Tom Solomon
author_sort Peter M. Winter
title Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
title_short Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
title_full Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
title_fullStr Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
title_full_unstemmed Proinflammatory cytokines and chemokines in humans with Japanese encephalitis
title_sort proinflammatory cytokines and chemokines in humans with japanese encephalitis
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/21506
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