Instituto Politécnico Nacional, Unidad Profesional Interdisciplinaria de Biotecnología, México City 07340, México.
MRC Centre for Drug Safety Science, Department of Pharmacology, University of Liverpool, Liverpool L69 3GE, United Kingdom.
Chem Res Toxicol. 2022 Jul 18;35(7):1162-1183. doi: 10.1021/acs.chemrestox.1c00434. Epub 2022 Jun 15.
Drugs can activate different cells of the immune system and initiate an immune response that can lead to life-threatening diseases collectively known as severe cutaneous adverse reactions (SCARs). Antibiotics, anticonvulsants, and antiretrovirals are involved in the development of SCARs by the activation of αβ naïve T-cells. However, other subsets of lymphocytes known as nonconventional T-cells with a limited T-cell receptor repertoire and innate and adaptative functions also recognize drugs and drug-like molecules, but their role in the pathogenesis of SCARs has only just begun to be explored. Despite 30 years of advances in our understanding of the mechanisms in which drugs interact with T-cells and the pathways for tissue injury seen during T-cell activation, at present, the development of useful clinical biomarkers for SCARs or predictive preclinical assays that could identify immunogenic moieties during drug discovery is an unmet goal. Therefore, the present review focuses on (i) advances in the understanding of the pathogenesis of SCARs reactions, (ii) a description of the interaction of drugs with conventional and nonconventional T-cells, and (iii) the current state of soluble blood circulating biomarker candidates for SCARs.
药物可激活免疫系统的不同细胞,引发免疫反应,从而导致危及生命的疾病,统称为严重皮肤不良反应(SCAR)。抗生素、抗惊厥药和抗逆转录病毒药物通过激活αβ幼稚 T 细胞,导致 SCAR 的发生。然而,其他被称为非传统 T 细胞的淋巴细胞亚群也具有有限的 T 细胞受体库和先天及适应性功能,它们也可以识别药物和类似药物的分子,但它们在 SCAR 发病机制中的作用才刚刚开始被探索。尽管我们对药物与 T 细胞相互作用的机制以及 T 细胞激活过程中组织损伤的途径的理解已经有 30 年的进展,但目前,SCAR 仍缺乏有用的临床生物标志物或预测性临床前检测方法,无法在药物发现过程中识别免疫原性部分。因此,本综述重点关注:(i)对 SCAR 反应发病机制的理解进展;(ii)药物与常规和非传统 T 细胞相互作用的描述;以及(iii)目前用于 SCAR 的可溶性循环血液生物标志物候选物的现状。