Division of Immunology, Children's Hospital Boston, Boston, Massachusetts, USA.
Ann N Y Acad Sci. 2012 Jan;1247:138-52. doi: 10.1111/j.1749-6632.2011.06263.x. Epub 2012 Jan 11.
Treatment for systemic lupus erythematosus (SLE) has traditionally been restricted to broad-based immunosuppression, with glucocorticoids being central to care. Recent insights into lupus pathogenesis promise new, selective therapies with more favorable side effect profiles. The best example of this is belimumab, which targets the B cell cytokine BLyS and has now received Food and Drug Administration (FDA) approval for its use in SLE. Strategies targeting other cytokines, such as interleukin 6 (IL-6) and interferon (IFN)-α, are also on the horizon. Blockade of costimulatory interactions between immune cells offers another opportunity for therapeutic intervention, as do small molecule inhibitors that interfere with cell signaling pathways. We review here the current strategies for SLE treatment, with particular focus on therapies now in active pharmaceutical development. We will also discuss new understandings in lupus pathogenesis that may lead to future advances in therapy.
治疗系统性红斑狼疮(SLE)传统上一直局限于广泛的免疫抑制治疗,糖皮质激素是治疗的核心。最近对狼疮发病机制的深入了解有望带来新的、选择性的治疗方法,具有更有利的副作用谱。这方面的最佳例子是贝利尤单抗,它针对 B 细胞细胞因子 BLyS,现已获得美国食品和药物管理局(FDA)批准用于治疗 SLE。针对其他细胞因子(如白细胞介素 6(IL-6)和干扰素(IFN)-α)的策略也即将出现。阻断免疫细胞之间的共刺激相互作用为治疗干预提供了另一个机会,小分子抑制剂干扰细胞信号通路也是如此。我们在这里回顾了 SLE 的治疗策略,特别关注目前处于药物研发阶段的疗法。我们还将讨论狼疮发病机制的新认识,这可能为未来的治疗进展提供依据。