Department of Molecular Science and Technology, Ajou University, Suwon, Korea.
J2H Biotech, Suwon, Korea.
Med Res Rev. 2019 May;39(3):1053-1090. doi: 10.1002/med.21553. Epub 2018 Nov 18.
Toll-like receptors (TLRs) are germline-encoded receptors that are central to innate and adaptive immune responses. Owing to their vital role in inflammation, TLRs are rational targets in clinics; thus, many ligands and biologics have been reported to overcome the progression of various inflammatory and malignant conditions and support the immune system. For each TLR, at least one, and often many, drug formulations are being evaluated. Ligands reported as stand-alone drugs may also be reported based on their use in combinatorial therapeutics as adjuvants. Despite their profound efficacy in TLR-modulation in preclinical studies, multiple drugs have been terminated at different stages of clinical trials. Here, TLR modulating drugs that have been evaluated in clinical trials are discussed, along with their mode of action, suggestive failure reasons, and ways to improve the clinical outcomes. This review presents recent advances in TLR-targeting drugs and provides directions for more successful immune system manipulation.
Toll 样受体(TLRs)是种系编码的受体,是先天和适应性免疫反应的核心。由于它们在炎症中的重要作用,TLRs 是临床治疗的合理靶点;因此,已报道了许多配体和生物制剂来克服各种炎症和恶性疾病的进展,并支持免疫系统。对于每种 TLR,至少有一种,通常有多种,药物制剂正在评估中。作为单一药物报道的配体也可能基于它们作为佐剂在联合治疗中的用途进行报道。尽管在临床前研究中在 TLR 调节方面具有深远的疗效,但许多药物已在临床试验的不同阶段终止。在这里,讨论了已在临床试验中评估的 TLR 调节药物,以及它们的作用模式、暗示的失败原因以及改善临床结果的方法。本综述介绍了 TLR 靶向药物的最新进展,并为更成功地进行免疫系统操纵提供了方向。