Table 3.
Novel therapeutic strategies in RA targeting multiple aspects of Th17 biology.
Drugs | Conceptual Th17 target | Molecular target | Stage of drug development |
---|---|---|---|
Anakinra | Differentiation | IL‐1 receptor | Approved for RA |
Tocilizumab | Differentiation | IL‐6 receptor | Approved for RA |
Ustekinumab | Differentiation and pathogenicity | IL‐23p40 | Approved for severe plaque psoriasis |
Statins | Differentiation and pathogenicity | Multiple | Efficacy proven in a RCT |
Auranofin | Differentiation and pathogenicity | Stat3 | Previously used |
CP‐690,550 (pan‐Jak inhibitor) | Differentiation and pathogenicity | IL‐6, 21, 23 signaling | Phase II trials suggest efficacy |
LY2439821 (Anti‐IL17A monoclonal antibody) | Pathogenicity | IL‐17A | Phase I trial completed |
IL‐21 receptor Fc fision protein | Differentiation | IL‐21 receptor | Animal study |
INCB028050 (Jak1/Jak2 inhibitor) | Differentiation and pathogenicity | IL‐6, 23 signaling | Animal study |
Monoclonal Ab againt IL‐23p19 | Differentiation and pathogenicity | IL‐23p19 | Not studied yet |
ROR‐c inhibitor | Differentiation | ROR‐c | Not studied yet |
Stat3 inhibitor | Differentiation and pathogenicity | Stat3 | Not studied yet |
Stat4 inhibitor | Differentiation and pathogenicity | Stat4 | Not studied yet |
DCs expressing TGF‐β | Differentiation | multiple | Not studied yet |
DCs expressing IFN‐γ/IL‐27/IL‐12/IL‐2/IL‐4 | Plasticity | Stats? | Not studied yet |
IL‐22 blockade | Pathogenicity? | IL‐22 | Awaits further studies |