The Kidney as a Reservoir for HIV-1 after Renal Transplantation

Guillaume Canaud(Brigham and Women's Hospital), Nathalie Dejucq‐Rainsford(Université de Rennes), Véronique Avettand-Fènoël(Sorbonne Paris Cité), Jean‐Paul Viard(Institut des Maladies Génétiques Imagine), Dany Anglicheau(Délégation Paris 5), Frank Bienaimé(Institut des Maladies Génétiques Imagine), Mordi Muorah(Délégation Paris 5), Louise Galmiche, Olivier Gribouval(Sorbonne Paris Cité), Laure‐Hélène Noël, Anne-Pascale Satié(Inserm), Frank Martinez(Inserm), Rébecca Sberro‐Soussan(Sorbonne Paris Cité), Anne Scemla(Institut des Maladies Génétiques Imagine), Marie-Claire Gübler(Sorbonne Paris Cité), Gérard Friedlander(Délégation Paris 5), Corinne Antignac(Institut des Maladies Génétiques Imagine), Marc‐Olivier Timsit(Structure Fédérative de Recherche en Biologie et Santé de Rennes), Andrea Onetti Muda(Università Campus Bio-Medico), Fabiola Terzi(Institut des Maladies Génétiques Imagine), Christine Rouzioux(Institut des Maladies Génétiques Imagine), Christophe Legendre(Sorbonne Paris Cité)
Journal of the American Society of Nephrology
December 5, 2013
Cited by 132

Abstract

Since the recent publication of data showing favorable outcomes for patients with HIV-1 and ESRD, kidney transplantation has become a therapeutic option in this population. However, reports have documented unexplained reduced allograft survival in these patients. We hypothesized that the unrecognized infection of the transplanted kidney by HIV-1 can compromise long-term allograft function. Using electron microscopy and molecular biology, we examined protocol renal transplant biopsies from 19 recipients with HIV-1 who did not have detectable levels of plasma HIV-1 RNA at transplantation. We found that HIV-1 infected the kidney allograft in 68% of these patients. Notably, HIV-1 infection was detected in either podocytes predominately (38% of recipients) or tubular cells only (62% of recipients). Podocyte infection associated with podocyte apoptosis and loss of differentiation markers as well as a faster decline in allograft function compared with tubular cell infection. In allografts with tubular cell infection, epithelial cells of the proximal convoluted tubules frequently contained abnormal mitochondria, and both patients who developed features of subclinical acute cellular rejection had allografts with tubular cell infection. Finally, we provide a novel noninvasive test for determining HIV-1 infection of the kidney allograft by measuring HIV-1 DNA and RNA levels in patients' urine. In conclusion, HIV-1 can infect kidney allografts after transplantation despite undetectable viremia, and this infection might influence graft outcome.


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