Copaescu Ana, Gibson Andrew, Li Yueran, Trubiano Jason A, Phillips Elizabeth J
Department of Infectious Diseases, Austin Health, Center for Antibiotic Allergy and Research, Heidelberg, VIC, Australia.
Immunology and Infectious Diseases, Murdoch University, Murdoch, WA, Australia.
Front Pharmacol. 2021 Jan 12;11:573573. doi: 10.3389/fphar.2020.573573. eCollection 2020.
Delayed drug hypersensitivity reactions are clinically diverse reactions that vary from isolated benign skin conditions that remit quickly with no or symptomatic treatment, drug discontinuation or even continued drug treatment, to the other extreme of severe cutaneous adverse reactions (SCARs) that are associated with presumed life-long memory T-cell responses, significant acute and long-term morbidity and mortality. Diagnostic "in clinic" approaches to delayed hypersensitivity reactions have included patch testing (PT), delayed intradermal testing (IDT) and drug challenges for milder reactions. Patch and IDT are, in general, performed no sooner than 4-6 weeks after resolution of the acute reaction at the maximum non-irritating concentrations. Functional and assays have largely remained the province of research laboratories and include lymphocyte transformation test (LTT) and cytokine release enzyme linked ImmunoSpot (ELISpot) assay, an emerging diagnostic tool which uses cytokine release, typically IFN-γ, after the patient's peripheral blood mononuclear cells are stimulated with the suspected drug(s). Genetic markers such as human leukocyte antigen have shown recent promise for both pre-prescription screening as well as pre-emptive and diagnostic testing strategies.
迟发性药物超敏反应是临床上多种多样的反应,从孤立的良性皮肤状况(这些状况在不治疗或进行对症治疗、停药甚至继续药物治疗的情况下会迅速缓解)到严重皮肤不良反应(SCARs)的另一个极端,后者与假定的终身记忆T细胞反应、显著的急性和长期发病率及死亡率相关。针对迟发性超敏反应的“临床”诊断方法包括斑贴试验(PT)、延迟皮内试验(IDT)以及针对较轻反应的药物激发试验。一般而言,斑贴试验和皮内试验在急性反应消退后至少4至6周,以最大无刺激浓度进行。功能检测在很大程度上仍局限于研究实验室,包括淋巴细胞转化试验(LTT)和细胞因子释放酶联免疫斑点(ELISpot)试验,ELISpot是一种新兴的诊断工具,在患者外周血单个核细胞用可疑药物刺激后,利用细胞因子释放(通常是IFN-γ)进行检测。诸如人类白细胞抗原等遗传标志物最近在处方前筛查以及抢先和诊断性检测策略方面显示出前景。