错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Mesenchymal stromal cells with chimaeric antigen receptors for enhanced immunosuppression

  • Olivia Sirpilla,
  • R. Leo Sakemura,
  • Mehrdad Hefazi,
  • Truc N. Huynh,
  • Ismail Can,
  • James H. Girsch,
  • Erin E. Tapper,
  • Michelle J. Cox,
  • Kendall J. Schick,
  • Claudia Manriquez-Roman,
  • Kun Yun,
  • Carli M. Stewart,
  • Ekene J. Ogbodo,
  • Brooke L. Kimball,
  • Long K. Mai,
  • Omar L. Gutierrez-Ruiz,
  • Makena L. Rodriguez,
  • Martina Gluscevic,
  • Daniel P. Larson,
  • Alex M. Abel,
  • Wesley A. Wierson,
  • Gloria Olivier,
  • Elizabeth L. Siegler,
  • Saad S. Kenderian

摘要

Allogeneic mesenchymal stromal cells (MSCs) are a safe treatment option for many disorders of the immune system. However, clinical trials using MSCs have shown inconsistent therapeutic efficacy, mostly owing to MSCs providing insufficient immunosuppression in target tissues. Here we show that antigen-specific immunosuppression can be enhanced by genetically modifying MSCs with chimaeric antigen receptors (CARs), as we show for E-cadherin-targeted CAR-MSCs for the treatment of graft-versus-host disease in mice. CAR-MSCs led to superior T-cell suppression and localization to E-cadherin+ colonic cells, ameliorating the animals’ symptoms and survival rates. On antigen-specific stimulation, CAR-MSCs upregulated the expression of immunosuppressive genes and receptors for T-cell inhibition as well as the production of immunosuppressive cytokines while maintaining their stem cell phenotype and safety profile in the animal models. CAR-MSCs may represent a widely applicable therapeutic technology for enhancing immunosuppression.