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    Renal transplant immunosuppression impairs natural killer cell function in Vitro and in vivo

    Access Status
    Open access via publisher
    Authors
    Morteau, O.
    Blundell, S.
    Chakera, Aron
    Bennett, S.
    Christou, C.
    Mason, P.
    Cornall, R.
    O'Callaghan, C.
    Date
    2010
    Type
    Journal Article
    
    Metadata
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    Citation
    Morteau, O. and Blundell, S. and Chakera, A. and Bennett, S. and Christou, C. and Mason, P. and Cornall, R. et al. 2010. Renal transplant immunosuppression impairs natural killer cell function in Vitro and in vivo. PLoS One. 5 (10).
    Source Title
    PLoS One
    DOI
    10.1371/journal.pone.0013294
    School
    Curtin Medical School
    URI
    http://hdl.handle.net/20.500.11937/24555
    Collection
    • Curtin Research Publications
    Abstract

    Background: Despite an increasing awareness of the importance of innate immunity, the roles of natural killer (NK) cells in transplant rejection and antiviral and cancer immunity during immunosuppression have not been clearly defined. Methods: To address this issue we have developed a quantitative assay of NK cell function that can be used on clinical samples and have studied the influence of immunosuppression on NK cell function. NK cell degranulation and intracellular interferon (IFN)-? production were determined by flow cytometry of peripheral blood samples. Results: Overnight ex vivo treatment of peripheral blood cells from healthy controls with ciclosporin or tacrolimus inhibited NK cell degranulation and IFN-? production in a dose-dependent manner. A similar impairment of function was seen in NK cells from patients treated in vivo with calcineurin inhibitors. In the early post-transplant period, there was a variable reduction of NK cell counts after treatment with alemtuzumab and basiliximab. Conclusions: The functional inhibition of NK cells in early transplant patients coincides with the period of maximum susceptibility to viral infections. The ability to assay NK cell function in clinical samples allows assessment of the impact of immunosuppression on these effector cells. This information may be helpful in guiding the titration of immunosuppression in the clinical setting. © 2010 Morteau et al.

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