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    Toll-like receptor (TLR) expression on CD4+ and CD8+ T-cells in patients chronically infected with hepatitis C virus

    Access Status
    Fulltext not available
    Authors
    Hammond, T.
    Lee, S.
    Watson, M.
    Flexman, J.
    Cheng, W.
    Fernandez, S.
    Price, Patricia
    Date
    2010
    Type
    Journal Article
    
    Metadata
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    Citation
    Hammond, T. and Lee, S. and Watson, M. and Flexman, J. and Cheng, W. and Fernandez, S. and Price, P. 2010. Toll-like receptor (TLR) expression on CD4+ and CD8+ T-cells in patients chronically infected with hepatitis C virus. Cellular Immunology. 264 (2): pp. 150-155.
    Source Title
    Cellular Immunology
    DOI
    10.1016/j.cellimm.2010.06.001
    ISSN
    0008-8749
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/47028
    Collection
    • Curtin Research Publications
    Abstract

    Toll-like receptor (TLR) expression on T-cells and the signalling pathways that lead to the production of cytokines may limit antigen-specific T-cell responses. Here, expression of TLR and retinoic acid inducible gene I (RIG-I) on T-cells were evaluated in patients chronically infected with hepatitis C virus (HCV), before and during pegylated interferon-a and ribavirin therapy. Expression of TLR2,3,4,7,9 and retinoic acid inducible gene (RIG)-I on different CD4+ and CD8+ T-cell sub-populations (naïve: CD45RA+CD57-; central memory: TCM CD45RA-CD57-; effector memory: TEM CD45RA-CD57+ and terminally differentiated effector memory: TEMRA CD45RA+CD57+) were measured by flow cytometry. TLR7, TLR9 and RIG-I expression on CD4+ T-cells and RIG-I expression on CD8+ T-cells was higher in patients than healthy controls. Therapy increased expression of TLR2, TLR4 and TLR9 and this was observed for all T-cell sub-populations. Evaluation of TLR expression at baseline did not identify patients able to achieve sustained virological response following therapy. © 2010.

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