American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2025
Donor-specific mesenchymal stem cell infusion in human and nonhuman primate kidney transplantation.
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Anwar Imran J, Li Shu, Mulvihill Michael, Schmitz Robin, Shaw Brian, Gao Qimeng, Swan-Nesbit Sherri, Cheatham Lynn A, How Tam, Miller Allison, Williams Kyha, Yin Fang-Fang, Giles William, Kurtzberg Joanne, Chandran Sindhu, Bridges Nancy, Lyakh Lyudmila, Breeden Cynthia, Gandhi Krupa, Sever Michelle, Song Mingqing, He Xu, Kirk Allan D
Аннотация
We report the results of 2 independent, concurrently performed studies evaluating the safety and efficacy of donor-derived mesenchymal stromal cell (MSC) infusions in inducing immune-tolerance in nonhuman primate (NHP) and human kidney transplant recipients treated with depletional induction and belatacept/sirolimus maintenance. Fifteen NHPs received rhesus ATG induction and were divided into 3 groups: control (n = 6), pretransplant thymic irradiation (n = 4), and thymic irradiation with monthly donor-MSC infusion (n = 5). Sirolimus was discontinued at day-180, and belatacept at day-365 posttransplant. In humans, 6 patients enrolled in ITN062ST underwent transplantation with alemtuzumab induction; 4 received 12 monthly donor-MSC infusions followed by immunosuppression withdrawal (ISW) if eligible. Donor-MSC infusion was acutely well tolerated in humans and NHPs. Chimerism was not established, and tolerance was not induced in either study. Two of the 5 NHPs that received MSCs rejected while on belatacept monotherapy with detectable donor-specific antibodies. Two patients did not initiate ISW due to de novo donor-specific antibodies and borderline rejection, and 2 patients failed ISW due to reversible rejection. In conclusion, donor MSCs can be given to NHPs or humans repeatedly without acute consequences, but they neither lead to detectable chimerism nor induce tolerance. In a subset of recipients, infused MSCs can be sensitizing.