Mesenchymal stromal cells with chimaeric antigen receptors for enhanced immunosuppression.
Olivia SirpillaR Leo SakemuraMehrdad HefaziTruc N HuynhIsmail CanJames H GirschErin E TapperMichelle J CoxKendall J SchickClaudia Manriquez-RomanKun YunCarli M StewartEkene J OgbodoBrooke L KimballLong K MaiOmar L Gutierrez-RuizMakena L RodriguezMartina GluscevicDaniel P LarsonAlex M AbelWesley A WiersonGloria OlivierElizabeth L SieglerSaad Sirop KenderianPublished in: Nature biomedical engineering (2024)
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.
Keyphrases
- mesenchymal stem cells
- umbilical cord
- bone marrow
- stem cells
- clinical trial
- gene expression
- stem cell transplantation
- poor prognosis
- cell therapy
- randomized controlled trial
- signaling pathway
- type diabetes
- genome wide
- drug delivery
- skeletal muscle
- dna methylation
- physical activity
- transcription factor
- open label
- cell proliferation
- depressive symptoms
- long non coding rna
- metabolic syndrome
- adipose tissue
- study protocol
- binding protein
- cancer therapy
- cell cycle arrest