Table 2.
Recognizes | Mechanism | Name | Type of Biologic | Studies in JIA-U |
---|---|---|---|---|
Tumor Necrosis Factor-α (TNF α) | Blocks inflammation mediated by TNF α | Etanercept | Soluble receptor | Y* |
Infliximab | Chimeric mAb* | Y | ||
Adalimumab | Humanized mAb | Y | ||
IL-17α | Interferes with TH17 function | Secukinumab | Humanized mAb | N* |
IL-6-receptor | Interferes with TH17 function and promote Treg function | tocilizumab | Humanized mAb | Y |
IL-12/IL-23 | Interfere with TH1 differentiation NK, CD8+ T cell function | Ustekinumab | Humanized mAb | N |
IL-1 receptor | Blocks IL-1 function | Anakinra, | IL-1 R antagonist | N |
IL-1beta | Canakinumab | mAb | N | |
IL-2R-alpha (CD25) | Blocks IL-2 signaling | Daclizumab§ | Humanized mAb | C* |
B7 | T cell/APC co-stimulation | Abatacept | CTLA4Ig fusion protein | C |
CD20 | Depletes B cells (save pro-B and plasma cells) | Rituximab | Chimeric mAb | C |
mAb, monoclonal antibody; Y, yes; N, no, C, case reports.
Not yet on the market.
Withdrawn from US market.