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      Increased Frequency of BK Virus-Specific Polyfunctional CD8+ T Cells Predict Successful Control of BK Viremia after Kidney Transplantation

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          Abstract

          Background

          BK virus infection remains an important cause of loss of allograft function after kidney transplantation. We sought to determine whether polyfunctional T cells secreting multiple cytokines simultaneously, which have been shown to be associated with viral control, could be detected early after start of BK viremia, which would provide insight into the mechanism of successful antiviral control.

          Methods

          Peripheral blood mononuclear cells collected during episodes of BK viral replication were evaluated by multiparameter flow cytometry after stimulation by overlapping peptide pools of BK virus antigen to determine frequency of CD8+ and CD4+ T cells expressing 1 or more cytokines simultaneously, as well as markers of T cell activation, exhaustion, and maturation.

          Results

          BK virus controllers, defined as those with episodes of BK viremia of 3 months or less, had an 11-fold increase in frequency of CD8+ polyfunctional T cells expressing multiple cytokines, as compared with patients with prolonged episodes of BK viremia. Patients with only low level BK viremia expressed low frequencies of polyfunctional T cells. Polyfunctional T cells were predominantly of the effector memory maturation subtype and expressed the cytotoxicity marker CD107a.

          Conclusions

          Noninvasive techniques for immune assessment of peripheral blood can provide insight into the mechanism of control of BK virus replication and may allow for future patient risk stratification and customization of immune suppression at the onset of BK viremia. 5

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          Author and article information

          Journal
          0132144
          7838
          Transplantation
          Transplantation
          Transplantation
          0041-1337
          1534-6080
          2 June 2016
          June 2017
          01 June 2018
          : 101
          : 6
          : 1479-1487
          Affiliations
          [1 ]Division of Infectious Diseases, David Geffen School of Medicine at UCLA, Los Angeles, CA
          [2 ]Department of Pathology and Laboratory Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA
          [3 ]Department of Biostatistics, UCLA School of Public Health, Los Angeles, CA
          [4 ]Division of Nephrology, David Geffen School of Medicine at UCLA, Los Angeles, CA
          [5 ]Department of Urology, David Geffen School of Medicine at UCLA, Los Angeles, CA
          Author notes
          [* ]Corresponding author: Joanna Schaenman, jschaenman@ 123456mednet.ucla.edu , David Geffen School of Medicine, Division of Infectious Diseases, 108333 LeConte Ave., CHS 37-121, Los Angeles, CA 90095
          Article
          PMC5219876 PMC5219876 5219876 nihpa784711
          10.1097/TP.0000000000001314
          5219876
          27391197
          373731d5-8d1c-4445-84c8-832040594bc1
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