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Anti-TNFα therapy for chronic inflammatory disease in kidney transplant recipients: Clinical outcomes. | LitMetric

Anti-TNFα therapy for chronic inflammatory disease in kidney transplant recipients: Clinical outcomes.

Medicine (Baltimore)

CHU Clermont-Ferrand, Department of Nephrology, Clermont-Ferrand Necker Hospital, Assistance Publique-Hôpitaux de Paris, Department of Nephrology and Kidney Transplantation, Paris CHU Rangueil, Nephrology, Dialysis, Transplantation, Toulouse CHU Pontchaillou, Department of Nephrology, Rennes CHU Clermont-Ferrand, Biostatistics Unit (DRCI), Clermont-Ferrand University Hospital, Nephrology-Transplantation Department, Strasbourg CHRU and FHU Transplantation, Department of Nephrology and Clinical Immunology, Tours CHU Clermont-Ferrand, Department of Rheutamology, Clermont-Ferrand Service de Néphrologie-Dialyse-Transplantation, CHU Angers, Angers Hôpital Maison Blanche-CHU Reims, Department of Nephrology, Reims Gastroenterology Department, University Hospital Estaing, Clermont-Ferrand Nephrology Department, Hôpital Européen Georges Pompidou, Assistance Publique Hôpitaux de Paris, Paris Department of Nephrology, CHU de Caen, Caen, France.

Published: October 2016

Anti-tumor necrosis factor-α (TNFα) therapy has improved the prognosis of many chronic inflammatory diseases. It appears to be well-tolerated by liver-transplant patients. However, their use and their safety in kidney-transplant patients have yet to be determined.In this retrospective study, we identified 16 adult kidney-transplant patients aged 46.5 years (34-51.8) who received anti-TNFα therapy from 7 kidney transplantation centers. The indications for this treatment included: chronic inflammatory bowel disease (n = 8), inflammatory arthritis (n = 5), AA amyloidosis (n = 1), psoriasis (n = 1), and microscopic polyangiitis (n = 1).Anti-TNFα therapies resulted in a clinical response in 13/16 patients (81%). Estimated glomerular filtration rates (MDRD-4) were similar on day 0 and at 24 months (M24) after anti-TNFα treatment had been initiated (41 [12-55] and 40 [21-53] mL/min/1.73 m, respectively). Two allograft losses were observed. The 1st case was due to antibody-mediated rejection (M18), while the 2nd was the result of AA amyloidosis recurrence (M20). There were several complications: 8 patients (50%) developed 23 serious infections (18 bacterial, 4 viral, and 1 fungal) and 4 developed cancer. Five patients died (infection n = 2, cardiac AA amyloidosis n = 1, intraalveolar hemorrhage following microscopic polyangiitis n = 1, and acute respiratory distress syndrome n = 1). On univariate analysis, recipient age associated with death (P = 0.009) and infection development (P = 0.06).Using anti-TNFα therapies, remission can be achieved in chronic inflammatory diseases in kidney-transplant patients. However, concommitant anti-TNFα and immunosuppresive therapies must be used with caution due to the high risk of infection, particularly after the age of 50.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072954PMC
http://dx.doi.org/10.1097/MD.0000000000005108DOI Listing

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