Monash Lupus Clinic, Department of Rheumatology, 46 Clayton Road, Clayton, Clayton 3168, Australia.
Expert Opin Biol Ther. 2012 Oct;12(10):1399-406. doi: 10.1517/14712598.2012.713934. Epub 2012 Aug 7.
In contrast to other areas in rheumatology, the therapeutic armamentarium in systemic lupus erythematosus (SLE) has lagged behind due to a number of reasons. While SLE is the prototypical multi-system autoimmune disease, its low incidence and the heterogeneity in its clinical manifestations have made it difficult to study. Despite advances in the understanding and application of immunology, the emergence of new targets has not been successfully validated largely due to the difficult-to-use outcome measures. Among the many targets studied, co-stimulation blockade that prevents activation of T cells by antigen-presenting cells, poses an interesting concept that is plausible based on basic science, animal and early human studies.
The authors hereby review the development of abatacept in the treatment of SLE and possible future directions.
Despite failure to achieve primary efficacy end points, the studies of abatacept in lupus provided tantalising evidence that co-stimulatory blockade is a feasible option worthy of further exploration.
与风湿病学的其他领域相比,由于多种原因,系统性红斑狼疮 (SLE) 的治疗手段一直滞后。虽然 SLE 是典型的多系统自身免疫性疾病,但由于其发病率低且临床表现存在异质性,因此难以进行研究。尽管在免疫学的理解和应用方面取得了进展,但由于难以使用的结果测量,新靶点的出现并没有得到成功验证。在研究的众多靶点中,共刺激阻断通过抗原呈递细胞阻止 T 细胞的激活,提出了一个有趣的概念,该概念基于基础科学、动物和早期人类研究具有合理性。
作者在此回顾了阿巴西普在治疗 SLE 中的发展以及可能的未来方向。
尽管未能达到主要疗效终点,但阿巴西普在狼疮中的研究提供了诱人的证据,表明共刺激阻断是一种可行的选择,值得进一步探索。