» Articles » PMID: 36484064

Autologous Mesenchymal Stem Cells for Treatment of Chronic Active Antibody-Mediated Kidney Graft Rejection: Report of the Phase I/II Clinical Trial Case Series

Abstract

Mesenchymal stem cell (MSCs) therapy has already been studied in kidney transplant recipients (KTRs), and the available data showed that it is safe and well tolerated. The aim of this study was to evaluate the safety and efficacy of autologous MSCs in combination with standard therapy in KTRs with biopsy-proven chronic active antibody-mediated rejection (AMR). Patients with biopsy-proven chronic active AMR received treatment with autologous bone marrow-derived MSCs (3 × 10 cells/kg iv) after completion of standard therapy and were followed for up to 12 months. The primary endpoints were safety by assessment of adverse events. Secondary endpoints included assessment of kidney graft function, immunological and histological changes related to AMR activity and chronicity assessed by conventional microscopy and molecular transcripts. A total of 3 patients were enrolled in the study before it was terminated prematurely because of adverse events. We found that AMR did not improve in any of the patients after treatment with MSCs. In addition, serious adverse events were observed in one case when autologous MSCs therapy was administered in the late phase after kidney transplantation, which requires further elucidation.

Citing Articles

The Promising Effect of Tocilizumab on Chronic Antibody-Mediated Rejection (cAMR) of Kidney Transplant.

Swiatek L, Miedziaszczyk M, Lewandowski D, Robakowski F, Tyburski P, Jakubowska M Pharmaceutics. 2025; 17(1).

PMID: 39861726 PMC: 11768637. DOI: 10.3390/pharmaceutics17010078.


Narrative Review of Mesenchymal Stem Cell Therapy in Renal Diseases: Mechanisms, Clinical Applications, and Future Directions.

Wang Y, Luo P, Wuren T Stem Cells Int. 2024; 2024:8658246.

PMID: 39698513 PMC: 11655143. DOI: 10.1155/sci/8658246.


Regulatory cell therapy for kidney transplantation and autoimmune kidney diseases.

Ho Q, Hester J, Issa F Pediatr Nephrol. 2024; 40(1):39-52.

PMID: 39278988 PMC: 11584488. DOI: 10.1007/s00467-024-06514-2.


The issue of heterogeneity of MSC-based advanced therapy medicinal products-a review.

cesnik A, Svajger U Front Cell Dev Biol. 2024; 12:1400347.

PMID: 39129786 PMC: 11310176. DOI: 10.3389/fcell.2024.1400347.


Comparing the Benefits and Drawbacks of Stem Cell Therapy Based on the Cell Origin or Manipulation Process: Addressing Immunogenicity.

Chang S, Park C Immune Netw. 2024; 23(6):e44.

PMID: 38188600 PMC: 10767552. DOI: 10.4110/in.2023.23.e44.


References
1.
Erpicum P, Weekers L, Detry O, Bonvoisin C, Delbouille M, Gregoire C . Infusion of third-party mesenchymal stromal cells after kidney transplantation: a phase I-II, open-label, clinical study. Kidney Int. 2018; 95(3):693-707. DOI: 10.1016/j.kint.2018.08.046. View

2.
El-Sayed M, El-Feky M, El-Amir M, Hasan A, Tag-Adeen M, Urata Y . Immunomodulatory effect of mesenchymal stem cells: Cell origin and cell quality variations. Mol Biol Rep. 2019; 46(1):1157-1165. DOI: 10.1007/s11033-018-04582-w. View

3.
Shi Y, Wang Y, Li Q, Liu K, Hou J, Shao C . Immunoregulatory mechanisms of mesenchymal stem and stromal cells in inflammatory diseases. Nat Rev Nephrol. 2018; 14(8):493-507. DOI: 10.1038/s41581-018-0023-5. View

4.
Waterman R, Tomchuck S, Henkle S, Betancourt A . A new mesenchymal stem cell (MSC) paradigm: polarization into a pro-inflammatory MSC1 or an Immunosuppressive MSC2 phenotype. PLoS One. 2010; 5(4):e10088. PMC: 2859930. DOI: 10.1371/journal.pone.0010088. View

5.
Wei Y, Chen X, Zhang H, Su Q, Peng Y, Fu Q . Efficacy and Safety of Bone Marrow-Derived Mesenchymal Stem Cells for Chronic Antibody-Mediated Rejection After Kidney Transplantation- A Single-Arm, Two-Dosing-Regimen, Phase I/II Study. Front Immunol. 2021; 12:662441. PMC: 8267917. DOI: 10.3389/fimmu.2021.662441. View