| Literature DB >> 25690781 |
Jose F Camargo1,2, Mariangela R Resende1,2,3, Ricardo Zamel1,4, William Klement5, Alyajahan Bhimji1,6, Sanja Huibner7, Deepali Kumar1,2, Atul Humar1,2, Igor Jurisica5, Shaf Keshavjee4, Rupert Kaul2,7, Shahid Husain1,2.
Abstract
CCR6 is a chemokine receptor involved in homing memory T cells, particularly Th17 cells, to sites of mucosal inflammation. Despite the critical role of memory T cells in long-term protective immunity against cytomegalovirus (CMV), a virus that reactivates at multiple mucosal sites, the ability of CCR6 or other Th17 marker expression to predict CMV reactivation following transplantation is not clear. Using 11-color flow cytometry, in this prospective single-center pilot study, we measured the expression of CCR6 and other markers of T-cell function in peripheral blood samples obtained from 21 SOT recipients at the time of discontinuation of anti-CMV prophylaxis. CMV viremia was monitored on a monthly basis after discontinuation of prophylaxis. Eleven patients (52%) developed CMV viremia during the six-month follow-up period. Late-onset CMV infection was preceded by an immune phenotype characterized by increased CCR6 expression on bulk CD4(+) T cells and a reduced number of circulating CMV IE-1-specific Th1 (CD4(+) IFN-γ(+)) cells. Among the markers evaluated, CCR6 was the best single predictor of late-onset CMV infection. Our results suggest that CCR6 expression at the time of discontinuation of antiviral prophylaxis might be a useful predictor of late-onset CMV reactivation and provide the basis for future larger prospective studies.Entities:
Keywords: T cell biology; cytomegalovirus; infection; infectious disease; viral
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Year: 2015 PMID: 25690781 DOI: 10.1111/ctr.12531
Source DB: PubMed Journal: Clin Transplant ISSN: 0902-0063 Impact factor: 2.863