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使用生物制剂靶向γc家族细胞因子:现状与未来前景

Targeting γc family cytokines with biologics: current status and future prospects.

作者信息

Bick Fabian, Blanchetot Christophe, Lambrecht Bart N, Schuijs Martijn J

机构信息

Argenx BV, Zwijnaarde, Belgium.

Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.

出版信息

MAbs. 2025 Dec;17(1):2468312. doi: 10.1080/19420862.2025.2468312. Epub 2025 Feb 18.

Abstract

Over the recent decades the market potential of biologics has substantially expanded, and many of the top-selling drugs worldwide are now monoclonal antibodies or antibody-like molecules. The common gamma chain (γc) cytokines, Interleukin (IL-)2, IL-4, IL-7, IL-9, IL-15, and IL-21, play pivotal roles in regulating immune responses, from innate to adaptive immunity. Dysregulation of cell signaling by these cytokines is strongly associated with a range of immunological disorders, which includes cancer as well as autoimmune and inflammatory diseases. Given the essential role of γc cytokines in maintaining immune homeostasis, the development of therapeutic interventions targeting these molecules poses unique challenges. Here, we provide an overview of current biologics targeting either single or multiple γc cytokines or their respective receptor subunits across a spectrum of diseases, primarily focusing on antibodies, antibody-like constructs, and antibody-cytokine fusions. We summarize therapeutic biologics currently in clinical trials, highlighting how they may offer advantages over existing therapies and standard of care, and discuss recent advances in this field. Finally, we explore future directions and the potential of novel therapeutic intervention strategies targeting this cytokine family.

摘要

在最近几十年里,生物制品的市场潜力大幅扩大,目前全球许多畅销药物都是单克隆抗体或抗体样分子。共同γ链(γc)细胞因子,即白细胞介素(IL-)2、IL-4、IL-7、IL-9、IL-15和IL-21,在调节从先天免疫到适应性免疫的免疫反应中发挥着关键作用。这些细胞因子的细胞信号失调与一系列免疫紊乱密切相关,其中包括癌症以及自身免疫性和炎症性疾病。鉴于γc细胞因子在维持免疫稳态中的重要作用,开发针对这些分子的治疗干预措施面临着独特的挑战。在这里,我们概述了目前针对单一或多种γc细胞因子或其各自受体亚基的生物制品在一系列疾病中的应用,主要关注抗体、抗体样构建体和抗体-细胞因子融合物。我们总结了目前正在进行临床试验的治疗性生物制品,强调它们相对于现有疗法和护理标准可能具有的优势,并讨论了该领域的最新进展。最后,我们探索针对该细胞因子家族的新型治疗干预策略的未来方向和潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7310/11845063/412036bfcb18/KMAB_A_2468312_F0001_OC.jpg

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