Regeneron Pharmaceuticals, Inc., Tarrytown, New York 10591, USA.
Ann N Y Acad Sci. 2009 Dec;1182:124-34. doi: 10.1111/j.1749-6632.2009.05074.x.
Rilonacept is a dimeric fusion protein consisting of the extracellular domains of interleukin (IL)-1 type 1 receptor and IL-1 receptor accessory protein joined to the constant region (Fc) of human immunoglobulin G1. By incorporating both components of the IL-1 binding complex, rilonacept is able to tightly bind IL-1 with picomolar affinity. Although early clinical results in rheumatoid arthritis (RA) suggested that RA is not primarily an IL-1-driven disease, the discovery that the rare genetic conditions called cryopyrin-associated periodic syndromes (CAPS) were caused by overproduction of IL-1 led to clinical development and approval for these conditions. An assay that detects rilonacept:IL-1 complexes in plasma is helping to identify new indications, such as gout, in which IL-1 overproduction plays a key pathogenic role. The development of rilonacept for CAPS was achieved through collaboration between the pharmaceutical industry, academia, and government agencies, and demonstrates that knowledge gleaned in orphan indications can inform drug development for more common and heterogeneous diseases.
利纳西普是一种二聚体融合蛋白,由白细胞介素 (IL)-1 型 1 受体和 IL-1 受体辅助蛋白的细胞外结构域与人类免疫球蛋白 G1 的恒定区 (Fc) 融合而成。通过结合 IL-1 结合复合物的两个组成部分,利纳西普能够以皮摩尔亲和力紧密结合 IL-1。尽管类风湿关节炎 (RA) 的早期临床结果表明 RA 不是主要由 IL-1 驱动的疾病,但发现称为冷球蛋白血症相关周期性综合征 (CAPS) 的罕见遗传疾病是由 IL-1 过度产生引起的,这导致了这些疾病的临床开发和批准。一种检测血浆中利纳西普:IL-1 复合物的检测方法正在帮助识别新的适应症,如痛风,其中 IL-1 过度产生发挥关键的致病作用。CAPS 利纳西普的开发是通过制药行业、学术界和政府机构的合作实现的,这表明从孤儿适应症中获得的知识可以为更常见和更具异质性的疾病的药物开发提供信息。