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    T cell receptor Vbeta gene usage in Thai children with dengue virus infection

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    Authors
    Gagnon, Susan J.
    Leporati, Anita M.
    Green, Sharone
    Kalayanarooj, Siripen
    Vaughn, David W.
    Stephens, Henry A. F.
    Suntayakorn, Saroj
    Kurane, Ichiro
    Ennis, Francis A.
    Rothman, Alan L.
    UMass Chan Affiliations
    Department of Medicine, Division of Infectious Diseases and Immunology
    Center for Infectious Disease and Vaccine Research
    Document Type
    Journal Article
    Publication Date
    2001-06-27
    Keywords
    Adolescent
    Child
    Child, Preschool
    Dengue
    Dengue Hemorrhagic Fever
    Female
    Genes, T-Cell Receptor beta
    Humans
    Infant
    Male
    Reverse Transcriptase Polymerase Chain Reaction
    Severity of Illness Index
    Thailand
    Immunology and Infectious Disease
    Pediatrics
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    Abstract
    T lymphocyte activation during dengue is thought to contribute to the pathogenesis of dengue hemorrhagic fever (DHF). We examined the T cell receptor Vbeta gene usage by a reverse transcriptase-polymerase chain reaction assay during infection and after recovery in 13 children with DHF and 13 children with dengue fever (DF). There was no deletion of specific Vbeta gene families. We detected significant expansions in usage of single Vbeta families in six subjects with DHF and three subjects with DF over the course of infection, but these did not show an association with clinical diagnosis, viral serotype, or HLA alleles. Differences in Vbeta gene usage between subjects with DHF and subjects with DF were of borderline significance. These data suggest that the differences in T cell activation in DHF and DF are quantitative rather than qualitative and that T cells are activated by conventional antigen(s) and not a viral superantigen.
    Source
    Am J Trop Med Hyg. 2001 Jan-Feb;64(1-2):41-8.
    DOI
    10.1164/rccm.2110097
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/38784
    PubMed ID
    11425161
    Related Resources
    Link to article in PubMed
    ae974a485f413a2113503eed53cd6c53
    10.1164/rccm.2110097
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