Review Article
Biological Therapy in Systemic Lupus Erythematosus
Table 1
Biological therapies proposed for SLE treatment.
| Biologic drug | Main results |
| B-cell targets |
| Anti-CD20 antibody | | Rituximab | Effective in treating refractory SLE [10, 11] Improvements in disease activity [12, 13] No benefit in proliferative lupus nephritis [14, 15] | Ocrelizumab | No benefit in lupus nephritis [16, 17] | Anti-CD22 antibody | | Epratuzumab | Improvement in BILAG scores [18] Reduction in corticosteroid doses with a good safety profile [19, 20] | B-lymphocyte tolerogens | | Abetimus | No long-term benefit in patients with lupus nephritis [21] | Edratide | No results released [22] | BLyS blockers | | Belimumab | Reduction in activity and new flares [23] | Atacicept | Significant decrease in IgM and IgG levels [24] |
| T-cell target and costimulatory blockers |
| Abatacept | Improvements in non-life- threatening SLE manifestations [25, 26] | IDEC-131 | No clinically effective in human SLE [27] | Efalizumab | Reduction in cutaneous SLE manifestations [28] | AMG557 | No results released [29] | Sirolimus | Safe and effective for refractory SLE [30] |
| Cytokine inhibition |
| Anti-TNF-α | | Infliximab | Long-term efficacy for lupus nephritis [31] | Anti-IFN-α/-γ | | Sifalimumab Rontalizumab AMG 811 | No results released [32] No results released [33] No results released [34] | Anti-IL-1 | | Anakinra | Improvements in SLE arthritis [35] | Anti-IL-6 | | Tocilizumab | Improvements in clinical and serologic responses [36] | Anti-IL-10 | | B-N10a | Improvements in disease activity [37] |
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aMurine Lupus; BILAG: The British Isles Lupus Assessment Group; BLyS: B cell survival molecule B lymphocyte stimulator; Ig: immunoglobulin; TNF: tumor necrosis factor; INF: interferon; IL:interleukin.
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