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dc.contributor.authorHatch, Steven
dc.contributor.authorEndy, Timothy P.
dc.contributor.authorThomas, Stephen J.
dc.contributor.authorMathew, Anuja
dc.contributor.authorPotts, James A.
dc.contributor.authorPazoles, Pamela P.
dc.contributor.authorLibraty, Daniel H.
dc.contributor.authorGibbons, Robert V.
dc.contributor.authorRothman, Alan L.
dc.date2022-08-11T08:11:05.000
dc.date.accessioned2022-08-23T17:32:40Z
dc.date.available2022-08-23T17:32:40Z
dc.date.issued2011-05-01
dc.date.submitted2012-06-22
dc.identifier.citation<p>J Infect Dis. 2011 May 1;203(9):1282-91. Epub 2011 Feb 18. <a href="http://dx.doi.org/10.1093/infdis/jir012">Link to article on publisher's site</a></p>
dc.identifier.issn0022-1899 (Linking)
dc.identifier.doi10.1093/infdis/jir012
dc.identifier.pmid21335561
dc.identifier.urihttp://hdl.handle.net/20.500.14038/50999
dc.description.abstractThe pathophysiology of dengue virus infection remains poorly understood, although secondary infection is strongly associated with more severe disease. In the present study, we performed a nested, case-control study comparing the responses of pre-illness peripheral blood mononuclear cells between children who would subsequently develop either subclinical or symptomatic secondary infection 6-11 months after the baseline blood samples were obtained and frozen. We analyzed intracellular cytokine production by CD4(+) and CD8(+) cells in response to stimulation with dengue antigen. We found higher frequencies of dengue virus-specific TNFalpha, IFNgamma-, and IL-2-producing T cells among schoolchildren who subsequently developed subclinical infection, compared with those who developed symptomatic secondary dengue virus infection. Although other studies have correlated immune responses during secondary infection with severity of disease, to our knowledge this is the first study to demonstrate a pre-infection dengue-specific immune response that correlates specifically with a subclinical secondary infection.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=21335561&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069729/
dc.subjectAdolescent
dc.subjectCase-Control Studies
dc.subjectChild
dc.subjectCytokines
dc.subjectDengue
dc.subjectDengue Virus
dc.subjectHumans
dc.subjectT-Lymphocytes
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectWomen's Studies
dc.titleIntracellular cytokine production by dengue virus-specific T cells correlates with subclinical secondary infection
dc.typeJournal Article
dc.source.journaltitleThe Journal of infectious diseases
dc.source.volume203
dc.source.issue9
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/534
dc.identifier.contextkey3017591
html.description.abstract<p>The pathophysiology of dengue virus infection remains poorly understood, although secondary infection is strongly associated with more severe disease. In the present study, we performed a nested, case-control study comparing the responses of pre-illness peripheral blood mononuclear cells between children who would subsequently develop either subclinical or symptomatic secondary infection 6-11 months after the baseline blood samples were obtained and frozen. We analyzed intracellular cytokine production by CD4(+) and CD8(+) cells in response to stimulation with dengue antigen. We found higher frequencies of dengue virus-specific TNFalpha, IFNgamma-, and IL-2-producing T cells among schoolchildren who subsequently developed subclinical infection, compared with those who developed symptomatic secondary dengue virus infection. Although other studies have correlated immune responses during secondary infection with severity of disease, to our knowledge this is the first study to demonstrate a pre-infection dengue-specific immune response that correlates specifically with a subclinical secondary infection.</p>
dc.identifier.submissionpathwfc_pp/534
dc.contributor.departmentDepartment of Medicine
dc.contributor.departmentGraduate School of Biomedical Sciences, Clinical and Population Health Research Program
dc.contributor.departmentCenter for Infectious Disease and Vaccine Research
dc.source.pages1282-91


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