双特异性抗体
医学
炎症性肠病
肿瘤坏死因子α
免疫学
计算生物学
免疫系统
抗体
临床试验
癌症研究
生物信息学
疾病
免疫疗法
管道(软件)
克罗恩病
叙述性评论
噬菌体展示
小分子
血液学
英夫利昔单抗
细胞因子
败血症
单克隆抗体
炎症性肠病
抗体反应
转化研究
抗原
作者
María Manuela Estevinho,Nurulamin M Noor
标识
DOI:10.1016/j.coph.2025.102596
摘要
There has been significant progress made in inflammatory bowel disease (IBD) over the last couple of decades, with a rapidly increasing number of biologic and small molecules treatments. Coupled with a better understanding of when and how to use treatments appropriately, this has resulted in substantial and meaningful improvement in outcomes for many patients. However, an ongoing issue is that around 30-40% of patients either do not respond or lose response to currently available treatments over time, underscoring the need for further novel therapeutic targets and approaches. Two particularly exciting novel approaches include a novel class of medications targeting tumor necrosis factor-like ligand 1A (TL1A) and the engagement in two pathogenic pathways simultaneously through the use of bispecific antibodies. The development of both of these potential treatment approaches has been built on decades of translational studies, including initial genetic discovery and immune functional validation. The class of molecules targeting TL1A has shown high potency in the pre-clinical setting and emerging data from early-phase interventional clinical trials have been encouraging. Bispecific antibodies have been used so far mostly in the fields of hematology and oncology, but with promising initial findings in IBD that targeting multiple pathways at once, may offer the prospect of greater remission rates or more durable remission than current strategies seeking to target single immunological pathways in isolation. This narrative review presents the latest evidence evaluating TL1A inhibition and bispecific antibodies, including the development pipeline for these molecules as innovative approaches for the next generation of IBD treatments.
科研通智能强力驱动
Strongly Powered by AbleSci AI