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Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin

BACKGROUND: Reactivation of BK polyoma virus causes a destructive virus allograft nephropathy (BKVAN) with graft loss in 46%. Treatment options are limited to reduced immunosuppression and largely ineffective antiviral agents. Some studies suggest benefit from intravenous immunoglobulin (IVIG). METH...

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Autores principales: Kable, Kathy, Davies, Carmen D., O'connell, Philip J., Chapman, Jeremy R., Nankivell, Brian John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381735/
https://www.ncbi.nlm.nih.gov/pubmed/28405598
http://dx.doi.org/10.1097/TXD.0000000000000641
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author Kable, Kathy
Davies, Carmen D.
O'connell, Philip J.
Chapman, Jeremy R.
Nankivell, Brian John
author_facet Kable, Kathy
Davies, Carmen D.
O'connell, Philip J.
Chapman, Jeremy R.
Nankivell, Brian John
author_sort Kable, Kathy
collection PubMed
description BACKGROUND: Reactivation of BK polyoma virus causes a destructive virus allograft nephropathy (BKVAN) with graft loss in 46%. Treatment options are limited to reduced immunosuppression and largely ineffective antiviral agents. Some studies suggest benefit from intravenous immunoglobulin (IVIG). METHODS: We evaluated effectiveness of adjuvant IVIG to eliminate virus from blood and tissue, in a retrospective, single-center cohort study, against standard-of-care controls. Both groups underwent reduced immunosuppression; conversion of tacrolimus to cyclosporine; and mycophenolate to leflunomide, oral ciprofloxacin, and intravenous cidofovir. RESULTS: Biopsy-proven BKVAN occurred in 50 kidneys at 7 (median interquartile range, 3-12) months after transplantation, predominantly as histological stage B (92%), diagnosed following by dysfunction in 46%, screening viremia in 20%, and protocol biopsy in 34%. After treatment, mean viral loads fell from 1581 ± 4220 × 10(3) copies at diagnosis to 1434 ± 70 639 midtreatment, and 0.138 ± 0.331 after 3 months (P < 0.001). IVIG at 1.01 ± 0.18 g/kg was given to 22 (44%) patients. The IVIG group more effectively cleared viremia (hazard ratio, 3.68; 95% confidence interval, 1.56-8.68; P = 0.003) and BK immunohistochemistry from repeated tissue sampling (hazard ratio, 2.24; 95% confidence interval, 1.09-4.58; P = 0.028), and resulted in faster (11.3 ± 10.4 months vs 29.1 ± 31.8 months, P = 0.015) and more complete resolution of viremia (33.3% vs 77.3%, P = 0.044). Numerically, fewer graft losses occurred with IVIG (27.3% vs 53.6% for control, P = 0.06), although graft and patient survivals were not statistically different. Acute renal dysfunction requiring pulse corticosteroid was common (59.1% vs 78.6%, P = 0.09), respectively, after immunosuppression reduction. CONCLUSIONS: Combination treatment incorporating adjuvant IVIG was more effective eliminating virus from BKVAN, compared with conventional therapy. Validation by multicenter randomized trial is needed.
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spelling pubmed-53817352017-04-12 Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin Kable, Kathy Davies, Carmen D. O'connell, Philip J. Chapman, Jeremy R. Nankivell, Brian John Transplant Direct Kidney Transplantation BACKGROUND: Reactivation of BK polyoma virus causes a destructive virus allograft nephropathy (BKVAN) with graft loss in 46%. Treatment options are limited to reduced immunosuppression and largely ineffective antiviral agents. Some studies suggest benefit from intravenous immunoglobulin (IVIG). METHODS: We evaluated effectiveness of adjuvant IVIG to eliminate virus from blood and tissue, in a retrospective, single-center cohort study, against standard-of-care controls. Both groups underwent reduced immunosuppression; conversion of tacrolimus to cyclosporine; and mycophenolate to leflunomide, oral ciprofloxacin, and intravenous cidofovir. RESULTS: Biopsy-proven BKVAN occurred in 50 kidneys at 7 (median interquartile range, 3-12) months after transplantation, predominantly as histological stage B (92%), diagnosed following by dysfunction in 46%, screening viremia in 20%, and protocol biopsy in 34%. After treatment, mean viral loads fell from 1581 ± 4220 × 10(3) copies at diagnosis to 1434 ± 70 639 midtreatment, and 0.138 ± 0.331 after 3 months (P < 0.001). IVIG at 1.01 ± 0.18 g/kg was given to 22 (44%) patients. The IVIG group more effectively cleared viremia (hazard ratio, 3.68; 95% confidence interval, 1.56-8.68; P = 0.003) and BK immunohistochemistry from repeated tissue sampling (hazard ratio, 2.24; 95% confidence interval, 1.09-4.58; P = 0.028), and resulted in faster (11.3 ± 10.4 months vs 29.1 ± 31.8 months, P = 0.015) and more complete resolution of viremia (33.3% vs 77.3%, P = 0.044). Numerically, fewer graft losses occurred with IVIG (27.3% vs 53.6% for control, P = 0.06), although graft and patient survivals were not statistically different. Acute renal dysfunction requiring pulse corticosteroid was common (59.1% vs 78.6%, P = 0.09), respectively, after immunosuppression reduction. CONCLUSIONS: Combination treatment incorporating adjuvant IVIG was more effective eliminating virus from BKVAN, compared with conventional therapy. Validation by multicenter randomized trial is needed. Lippincott Williams & Wilkins 2017-03-10 /pmc/articles/PMC5381735/ /pubmed/28405598 http://dx.doi.org/10.1097/TXD.0000000000000641 Text en Copyright © 2017 The Author(s). Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Kidney Transplantation
Kable, Kathy
Davies, Carmen D.
O'connell, Philip J.
Chapman, Jeremy R.
Nankivell, Brian John
Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title_full Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title_fullStr Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title_full_unstemmed Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title_short Clearance of BK Virus Nephropathy by Combination Antiviral Therapy With Intravenous Immunoglobulin
title_sort clearance of bk virus nephropathy by combination antiviral therapy with intravenous immunoglobulin
topic Kidney Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381735/
https://www.ncbi.nlm.nih.gov/pubmed/28405598
http://dx.doi.org/10.1097/TXD.0000000000000641
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