Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
J Allergy Clin Immunol Pract. 2022 May;10(5):1155-1167.e5. doi: 10.1016/j.jaip.2022.02.004. Epub 2022 Feb 15.
Drug-induced hypersensitivity syndrome/drug reaction with eosinophilia and systemic symptoms (DIHS/DRESS) is one example of a severe delayed T-cell-mediated adverse drug reaction. DIHS/DRESS presents with fever, widespread rash and facial edema, organ involvement, and hematological abnormalities, including eosinophilia and atypical lymphocytosis. DIHS/DRESS is associated with relapse 2 to 4 weeks after acute symptoms, often coinciding with reactivation of prevalent chronic persistent human herpesviruses such as human herpesvirus 6, EBV, and cytomegalovirus. The mortality of DIHS/DRESS is up to 10% and often related to unrecognized myocarditis and cytomegalovirus complications, with longer-term consequences that contribute to morbidity including autoimmune diseases such as thyroiditis. It is essential that all potential drug causes, including all new drugs introduced within the 8 weeks preceding onset of DIHS/DRESS symptoms, are identified. All potential drug culprits, as well as drugs that are closely related structurally to the culprit drug, should be avoided in the future. Systemic corticosteroids have remained the mainstay for the treatment of DIHS/DRESS with internal organ involvement. Steroid-sparing agents, such as cyclosporine, mycophenolate mofetil, and monthly intravenous immune globulin, have been successfully used for treatment, and careful follow-up for cytomegalovirus reactivation is recommended. Strong associations between HLA class I alleles and DIHS/DRESS predisposition include HLA-B∗13:01 and dapsone, HLA-B∗58:01 and allopurinol, and HLA-B∗32:01 and vancomycin. These have opened a pathway for prevention, risk stratification, and earlier diagnosis. Single-cell sequencing and other studies of immunopathogenesis promise to identify targeted treatment approaches.
药物诱导的超敏反应综合征/伴有嗜酸性粒细胞增多和全身症状的药物反应(DIHS/DRESS)是一种严重的迟发性 T 细胞介导的药物不良反应。DIHS/DRESS 表现为发热、广泛皮疹和面部水肿、器官受累和血液学异常,包括嗜酸性粒细胞增多和非典型淋巴细胞增多。DIHS/DRESS 与急性症状后 2 至 4 周的复发有关,通常与常见的慢性持续性人类疱疹病毒(如人类疱疹病毒 6、EBV 和巨细胞病毒)的重新激活同时发生。DIHS/DRESS 的死亡率高达 10%,且常与未被识别的心肌炎和巨细胞病毒并发症有关,其长期后果导致发病率增加,包括甲状腺炎等自身免疫性疾病。确定所有潜在的药物原因,包括 DIHS/DRESS 症状发作前 8 周内引入的所有新药,是至关重要的。所有潜在的药物罪魁祸首,以及与罪魁祸首药物结构密切相关的药物,都应在未来避免使用。对于伴有内脏器官受累的 DIHS/DRESS,全身性皮质类固醇仍然是主要的治疗方法。环孢素、霉酚酸酯和每月静脉注射免疫球蛋白等类固醇节约剂已成功用于治疗,建议密切随访巨细胞病毒再激活情况。HLA Ⅰ类等位基因与 DIHS/DRESS 易感性之间存在强烈关联,包括 HLA-B∗13:01 和氨苯砜、HLA-B∗58:01 和别嘌醇,以及 HLA-B∗32:01 和万古霉素。这些为预防、风险分层和早期诊断开辟了途径。单细胞测序和免疫发病机制的其他研究有望确定靶向治疗方法。