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Expression of TIM-3 on Plasmacytoid Dendritic Cells as a Predictive Biomarker of Decline in HIV-1 RNA Level during ART

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    SYSNO ASEP0494673
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleExpression of TIM-3 on Plasmacytoid Dendritic Cells as a Predictive Biomarker of Decline in HIV-1 RNA Level during ART
    Author(s) Font-Haro, Albert (UMG-J)
    Janovec, Vaclav (UMG-J)
    Hofman, T. (CZ)
    Machala, L. (CZ)
    Jilich, D. (CZ)
    Mělková, Z. (CZ)
    Weber, J. (CZ)
    Trejbalová, Kateřina (UMG-J) RID
    Hirsch, Ivan (UMG-J) ORCID, RID
    Number of authors9
    Article number154
    Source TitleViruses. - : MDPI
    Roč. 10, č. 4 (2018)
    Number of pages13 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordshiv-1 ; antiretroviral therapy (ART) ; innate and adaptive immune responses ; plasmacytoid dendritic cells (pDCs) ; pDC dysfunction ; T cell Ig and mucin-domain containing molecule 3 (TIM-3) ; bdca-2 ; Toll-like receptors 7 and 9 (TLR7/9)
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryVirology
    R&D ProjectsGA14-32547S GA ČR - Czech Science Foundation (CSF)
    ED1.1.00/02.0109 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    LQ1604 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportUMG-J - RVO:68378050
    UT WOS000435184400015
    DOI10.3390/v10040154
    AnnotationDepletion and functional impairment of circulating plasmacytoid dendritic cells (pDCs) are characteristic attributes of HIV-1-infection. The mechanism of dysfunction of pDCs is unclear. Here, we studied the development of phenotype of pDCs in a cohort of HIV-1-infected individuals monitored before the initiation and during a 9-month follow up with antiretroviral therapy (ART). Using polychromatic flow cytometry, we detected significantly higher pDC-surface expression of the HIV-1 receptor CD4, regulatory receptor BDCA-2, Fcy receptor CD32, pDC dysfunction marker TIM-3, and the marker of killer pDC, TRAIL, in treatment-naive HIV-1-infected individuals before initiation of ART when compared to healthy donors. After 9 months of ART, all of these markers approached but did not reach the expression levels observed in healthy donors. We found that the rate of decline in HIV-1 RNA level over the first 3 months of ART negatively correlated with the expression of TITM-3 on pDCs. We conclude that immunogenic phenotype of pDCs is not significantly restored after sustained suppression of HIV-1 RNA level in ART-treated patients and that the level of the TIM-3 expressed on pDCs in treatment naive patients could be a predictive marker of the rate of decline in the HIV-1 RNA level during ART.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2019
Number of the records: 1  

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