4.7 Article

Infusion of third-party mesenchymal stromal cells after kidney transplantation: a phase I-II, open-label, clinical study

期刊

KIDNEY INTERNATIONAL
卷 95, 期 3, 页码 693-707

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2018.08.046

关键词

cell therapy; kidney transplantation; mesenchymal stromal cells

资金

  1. FNRS
  2. University of Liege (Fonds Speciaux a la Recherche - Fonds Leon Fredericq [ACiiRT])
  3. Fonds d'investissement de recherche scientifique (FIRS) of CHU of Liege
  4. Foundation against Cancer
  5. Federal Cancer Plan - Belgium

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Mesenchymal stromal cells (MSCs) exhibit anti-inflammatory and immune-regulatory properties, and preclinical studies suggest a potential benefit in solid organ transplantation. We report on the 1-year follow-up of an open-label phase I-II trial of a single infusion of third-party MSC post-kidney transplantation, in addition to standard immunosuppression. Ten kidney transplant recipients from deceased donors received third-party bone marrow MSCs (similar to 2 x 10(6)/kg) on day 3 +/- 2 post-transplant and were compared to 10 concurrent controls. No adverse effects were noted at MSC injection. One participant with a history of cardiac disease had a non-ST-elevation myocardial infarction approximately 3 hours after MSC infusion. Incidences of opportunistic infections and acute rejection were similar. At day 7 post-transplant, estimated glomerular filtration rate (eGFR) in MSC-treated recipients reached 48.6 ml/min/1.73m(2), compared to 32.5 ml/min/1.73m(2) in controls and 29.3 ml/min/1.73m(2) in our overall cohort of kidney transplant recipients. No difference in eGFR was found at 1 year. MSC-treated recipients showed increased frequencies of regulatory T cells at day 30, with no significant change in B cell frequencies compared to concurrent controls. Four MSC-treated participants developed antibodies against MSC or shared kidney-MSC HLA, with only 1 with MFI > 1500. A single infusion of third-party MSC following kidney transplantation appears to be safe, with one cardiac event of unclear relationship to the intervention. MSC therapy is associated with increased regulatory T cell proportion and with improved early allograft function. Long-term effects, including potential immunization against MSC, remain to be studied.

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