Table 3.
Immunoactive compounds with Treg-enhancing capacity
| Compound | Effect on Treg | Results in experimental autoimmune disease | Results in human autoimmune disease |
|---|---|---|---|
| Anti-CD3 antibodies | Treg induction | Complete and sustained remission in recent-onset diabetic NOD mice [56] | Long-term improved insulin production in new-onset Type 1 diabetes [52, 53] |
| Short-term improvement in the number of inflamed joints in PsA [54] | |||
| Neuropeptides | Treg induction, expansion and enhanced function | VIP reduces development of CIA and established disease in DBA/1J mice [57, 63] | – |
| Urocortin reduces severity of established CIA in DBA/1J mice [64] | |||
| Retinoic acid | Treg induction | Reduced incidence of diabetes in NOD mice with established insulitis [70] | – |
| Improved bodyweight and reduced colon inflammation in TNBS-induced colitis [71] | |||
| Reduced severity and incidence of CIA in DBA/1J mice [72] | |||
| HDAC inhibitors | Enhancement and stabilization of FOXP3 expression leading to enhanced function | TSA and SAHA prevent bodyweight loss and histological damage in DSS-induced colitis [80, 81] | – |
| TSA reduces development of renal pathology in lupus-prone NZB/W F1 mice [82] | |||
| VPA reduces the incidence and severity of CIA in DBA/1J mice [83] |
NOD: non-obese diabetic; TNBS: trinitrobenzene sulfonic acid; DSS: dextran sodium sulphate.