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. 2010 May 12;49(9):1632–1644. doi: 10.1093/rheumatology/keq130

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.