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      BK Virus Load Associated with Serum Levels of sCD30 in Renal Transplant Recipients

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          Abstract

          Background. Rejection is the main drawback facing the renal transplant operations. Complicated and overlapping factors, mainly related to the immune system, are responsible for this rejection. Elevated serum levels of sCD30 were frequently recorded as an indicator for renal allograft rejection, while BV virus is considered as one of the most serious consequences for immunosuppressive treatment of renal transplant recipients (RTRs). Aims. This study aimed to determine the association of BK virus load with serum levels of sCD30 in RTRs suffering from nephropathy. Patients and Methods. A total of 50 RTRs with nephropathy and 30 age-matched apparently healthy individuals were recruited for this study. Serum samples were obtained from each participant. Real-time PCR was used to quantify BK virus load in RTRs serum, while ELISA technique was employed to estimate serum levels of sCD30. Results. Twenty-two percent of RTRs had detectable BKV with mean viral load of 1.094 E + 06 ± 2.291 E + 06. RTRs showed higher mean serum level of sCD30 (20.669 ± 18.713 U/mL) than that of controls (5.517 ± 5.304 U/mL) with significant difference. BK virus load had significant positive correlation with the serum levels of sCD30 in RTRs group. Conclusion. These results suggest that serum levels of sCD30 could be used as an indicator of BK viremia, and accordingly the immunosuppressive regime should be adjusted.

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          Most cited references28

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          The TNF receptor superfamily of cellular and viral proteins: activation, costimulation, and death.

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            BK polyomavirus in solid organ transplantation.

            The human BK polyomavirus (BKV) is the major cause of polyomavirus-associated nephropathy (PyVAN) putting 1-15% of kidney transplant patients at risk of premature allograft failure, but is less common in other solid organ transplants. Because effective antiviral therapies are lacking, screening kidney transplant patients for BKV replication in urine and blood has become the key recommendation to guide the reduction of immunosuppression in patients with BKV viremia. This intervention allows for expanding BKV-specific cellular immune responses, curtailing of BKV replication in the graft, and clearance of BKV viremia in 70-90% patients. Postintervention rejection episodes occur in 8-12%, most of which are corticosteroid responsive. Late diagnosis is faced with irreversible functional decline, poor treatment response, and graft loss. Adjunct therapies such as cidofovir, leflunomide and intravenous immunoglobulins have been used, but the benefit is not documented in trials. Retransplantation after PyVAN is largely successful, but requires close monitoring for recurrent BKV viremia. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.
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              CD30 (Ki-1) molecule: a new cytokine receptor of the tumor necrosis factor receptor superfamily as a tool for diagnosis and immunotherapy.

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                Author and article information

                Journal
                Int J Microbiol
                Int J Microbiol
                IJMICRO
                International Journal of Microbiology
                Hindawi Publishing Corporation
                1687-918X
                1687-9198
                2016
                9 March 2016
                : 2016
                : 9752097
                Affiliations
                1Medical research Unit, School of Medicine, University of Al-Nahrain, Baghdad 10066, Iraq
                2Medical Technical Institute, Baghdad 10066, Iraq
                3Biotechnology Department, School of Science, University of Baghdad, Baghdad 10066, Iraq
                4Biology Department, School of Science, University of Al-Mustansiriyah, Baghdad 10066, Iraq
                Author notes

                Academic Editor: Carla R. Arciola

                Author information
                http://orcid.org/0000-0003-2888-4840
                Article
                10.1155/2016/9752097
                4804059
                27051424
                9889efb3-06e6-4be2-9c51-0c330e649419
                Copyright © 2016 Haidar A. Shamran et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 3 December 2015
                : 10 February 2016
                : 15 February 2016
                Categories
                Research Article

                Microbiology & Virology
                Microbiology & Virology

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