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  • The immune checkpoint CD96 defines a distinct lymphocyte phenotype and is highly expressed on tumor-infiltrating T cells

    Author(s)
    Lepletier, Ailin
    Lutzky, Viviana P
    Mittal, Deepak
    Stannard, Kimberley
    Watkins, Thomas S
    Ratnatunga, Champa N
    Smith, Corey
    McGuire, Helen M
    Kemp, Roslyn A
    Mukhopadhyay, Pamela
    Waddell, Nicola
    Smyth, Mark J
    Dougall, William C
    Miles, John J
    Griffith University Author(s)
    Lepletier de Oliveira, Ailin
    Year published
    2019
    Metadata
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    Abstract
    CD96 has recently been shown to be a potent immune checkpoint molecule in mice, but a similar role in humans is not known. In this study, we provide a detailed map of CD96 expression across human lymphocyte lineages, the kinetics of CD96 regulation on T‐cell activation and co‐expression with other conventional and emerging immune checkpoint molecules. We show that CD96 is predominantly expressed by T cells and has a unique lymphocyte expression profile. CD96high T cells exhibited distinct effector functions on activation. Of note, CD96 expression was highly correlated with T‐cell markers in primary and metastatic human tumors ...
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    CD96 has recently been shown to be a potent immune checkpoint molecule in mice, but a similar role in humans is not known. In this study, we provide a detailed map of CD96 expression across human lymphocyte lineages, the kinetics of CD96 regulation on T‐cell activation and co‐expression with other conventional and emerging immune checkpoint molecules. We show that CD96 is predominantly expressed by T cells and has a unique lymphocyte expression profile. CD96high T cells exhibited distinct effector functions on activation. Of note, CD96 expression was highly correlated with T‐cell markers in primary and metastatic human tumors and was elevated on antigen‐experienced T cells and tumor‐infiltrating lymphocytes. Collectively, these data demonstrate that CD96 may be a promising immune checkpoint to enhance T‐cell function against human cancer and infectious disease.
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    Journal Title
    Immunology and Cell Biology
    DOI
    https://doi.org/10.1111/imcb.12205
    Note
    This publication has been entered into Griffith Research Online as an Advanced Online Version.
    Subject
    Biochemistry and cell biology
    Biochemistry and cell biology not elsewhere classified
    Immunology
    Publication URI
    http://hdl.handle.net/10072/382282
    Collection
    • Journal articles

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