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Infusion of third-party mesenchymal stromal cells after kidney transplantation: a phase I-II, open-label, clinical study.
Erpicum, Pauline; Weekers, Laurent; Detry, Olivier; Bonvoisin, Catherine; Delbouille, Marie-Hélène; Grégoire, Céline; Baudoux, Etienne; Briquet, Alexandra; Lechanteur, Chantal; Maggipinto, Gianni; Somja, Joan; Pottel, Hans; Baron, Frédéric; Jouret, François; Beguin, Yves.
Afiliação
  • Erpicum P; Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; Groupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Cardiovascular Sciences, University of Liège (ULiège), Liège, Belgium.
  • Weekers L; Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Detry O; Groupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Cardiovascular Sciences, University of Liège (ULiège), Liège, Belgium; Division of Abdominal Surgery and Transplantation, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Bonvoisin C; Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Delbouille MH; Division of Abdominal Surgery and Transplantation, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Grégoire C; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; GIGA, I3-Hematology, University of Liège (ULiège), Liège, Belgium; Division of Hematology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Baudoux E; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Briquet A; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Lechanteur C; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Maggipinto G; Division of Immunohematology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Somja J; Division of Pathology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Pottel H; KU Leuven Kulak, Department of Public Health and Primary Care, University of Leuven, Kortrijk, Belgium.
  • Baron F; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; GIGA, I3-Hematology, University of Liège (ULiège), Liège, Belgium; Division of Hematology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
  • Jouret F; Division of Nephrology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; Groupe Interdisciplinaire de Génoprotéomique Appliquée (GIGA), Cardiovascular Sciences, University of Liège (ULiège), Liège, Belgium. Electronic address: francois.jouret@chuliege.be.
  • Beguin Y; Laboratory of Cell and Gene Therapy (LTCG), CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium; GIGA, I3-Hematology, University of Liège (ULiège), Liège, Belgium; Division of Hematology, CHU of Liège, University of Liège (CHU ULiège), Liège, Belgium.
Kidney Int ; 95(3): 693-707, 2019 03.
Article em En | MEDLINE | ID: mdl-30528263
ABSTRACT
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 (∼2 × 106/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/1.73m2, compared to 32.5 ml/min/1.73m2 in controls and 29.3 ml/min/1.73m2 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia de Imunossupressão / Transplante de Rim / Transplante de Células-Tronco Mesenquimais / Rejeição de Enxerto / Falência Renal Crônica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Kidney Int Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terapia de Imunossupressão / Transplante de Rim / Transplante de Células-Tronco Mesenquimais / Rejeição de Enxerto / Falência Renal Crônica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Kidney Int Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bélgica
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