Table 2.
Type of therapy | Clinical/preclinical model | Outcomes |
---|---|---|
Corticosteroids | Immunosuppression in transplant patients affects Treg number and function, reviewed in (11) | Effective in preventing rejection, associated with short- and long-term adverse events (81) |
Adoptive transfer(PolyTregs) | Phase I clinical trial demonstrating safety of polyTreg therapy in addition to IL-2 therapy (68) | Operational tolerance achieved in 7/10 patients (71) Risk of infection |
Adoptive transfer (arTregs) | arTregs successfully home to the liver and prevent allograft rejection in preclinical skin graft model (82) | arTregs are significantly more effective than polyTregs (64, 82) |
CAR-Tregs | Tailored Treg specificity using CARs specific for antigens relevant to liver transplantation. (83–86) |
Encouraging results in human and preclinical skin allograft models (87, 88) |
Enclysis Inhibitor | Enclysis inhibitors should be tested alongside current immunosuppression regimens in liver transplantation | Enclysis inhibitors could potentiate immunosuppression |
PolyTreg, Polyclonally-expanded regulatory T cells; arTreg, Alloantigen-reactive regulatory T cells; CAR, Chimeric Antigen Receptor.