| Literature DB >> 20430180 |
C-H Chen1, M-C Wen, M Wang, J-D Lian, C-H Cheng, M-J Wu, T-M Yu, Y-W Chuang, D Chang, K-H Shu.
Abstract
Human polyomaviruses (PV), including JC and BK virus, have been reported to cause polyomavirus-associated nephropathy (PVAN), in renal transplant patients. PV infection has been demonstrated to be associated with malignancies in animals; however, the association between malignancy and viral infections in humans is not clear. We retrospectively reviewed our 864 (M:F=502:362) kidney transplant patients over the past 25 years. We identified PVAN in 6 patients (0.69%), including BK nephropathy (n=5) and JC nephropathy (n=1). Three patients (50%) improved after reducing the immunosuppression, but 3 (50%) progressed to graft loss despite this reduction. Malignancy occurred in 5 out of the 6 patients (83%; P<.0001 compared with patients without PVAN), including transitional cell carcinoma (n=2), renal cell carcinoma (n=1), squamous cell carcinoma of skin (n=1) and Kaposi sarcoma (n=1). We concluded that kidney transplant patients with PVAN are at a significantly greater risk to develop malignancy. Whether this is due to a direct effect of PV infection or the result of overimmunosuppression remains to be determined in a future study. Copyright (c) 2010 Elsevier Inc. All rights reserved.Entities:
Mesh:
Year: 2010 PMID: 20430180 DOI: 10.1016/j.transproceed.2010.02.068
Source DB: PubMed Journal: Transplant Proc ISSN: 0041-1345 Impact factor: 1.066