Human umbilical cord-derived mesenchymal stromal cells for the treatment of steroid refractory grades III-IV acute graft-versus-host disease with long-term follow-up

Front Immunol. 2024 Aug 15:15:1436653. doi: 10.3389/fimmu.2024.1436653. eCollection 2024.

Abstract

Introduction: Mesenchymal stromal cells (MSCs) have been extensively studied as a potential treatment for steroid refractory acute graft-versus-host disease (aGVHD). However, the majority of clinical trials have focused on bone marrow-derived MSCs.

Methods: In this study, we report the outcomes of 86 patients with grade III-IV (82.6% grade IV) steroid refractory aGVHD who were treated with human umbilical cord-derived mesenchymal stromal cells (UC-MSCs). The patient cohort included 17 children and 69 adults. All patients received intravenous infusions of UC-MSCs at a dose of 1 × 106 cells per kg body weight, with a median of 4 infusions (ranging from 1 to 16).

Results: The median time between the onset of aGVHD and the first infusion of UC-MSCs was 7 days (ranging from 3 to 88 days). At day 28, the overall response (OR) rate was 52.3%. Specifically, 24 patients (27.9%) achieved complete remission, while 21 (24.4%) exhibited partial remission. The estimated survival probability at 100 days was 43.7%. Following a median follow-up of 108 months (ranging from 61 to 159 months), the survival rate was approximately 11.6% (10/86). Patients who developed acute lower GI tract and liver GVHD exhibited poorer OR rates at day 28 compared to those with only acute lower GI tract GVHD (22.2% vs. 58.8%; p= 0.049). No patient experienced serious adverse events.

Discussion: These finding suggest that UC-MSCs are safe and effective in both children and adults with steroid refractory aGVHD. UC-MSCs could be considered as a feasible treatment option for this challenging conditon. (NCT01754454).

Keywords: graft-versus-host disease; hematopoietic stem cell transplantation; long-term follow-up; mesenchymal stromal cells; umbilical cord.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II

MeSH terms

  • Acute Disease
  • Adult
  • Child
  • Feasibility Studies
  • Follow-Up Studies
  • Graft vs Host Disease* / mortality
  • Graft vs Host Disease* / therapy
  • Humans
  • Mesenchymal Stem Cell Transplantation* / adverse effects
  • Mesenchymal Stem Cell Transplantation* / methods
  • Mesenchymal Stem Cells*
  • Steroids / pharmacology
  • Steroids / therapeutic use
  • Treatment Outcome
  • Umbilical Cord* / cytology

Substances

  • Steroids

Associated data

  • ClinicalTrials.gov/NCT01754454

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The study was funded by the National High-Tech R&D Program (863 Program) (NO.2013AA020103) and the Science and Technology Plan of Beijing City (NO.Z111107058811107). The funding body covered the spendings on preparation of the MSCs, and collection and interpretation of data.