Peter Jonathan Grant, Lehloenya Rannakoe, Dlamini Sipho, Risma Kimberly, White Katie D, Konvinse Katherine C, Phillips Elizabeth J
Division of Allergology and Clinical Immunology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Division of Dermatology, Department of Medicine, University of Cape Town, Cape Town, South Africa.
J Allergy Clin Immunol Pract. 2017 May-Jun;5(3):547-563. doi: 10.1016/j.jaip.2017.01.025.
Most immune-mediated adverse drug reactions (IM-ADRs) involve the skin, and many have additional systemic features. Severe cutaneous adverse drug reactions (SCARs) are an uncommon, potentially life-threatening, and challenging subgroup of IM-ADRs with diverse clinical phenotypes, mechanisms, and offending drugs. T-cell-mediated immunopathology is central to these severe delayed reactions, but effector cells and cytokines differ by clinical phenotype. Strong HLA-gene associations have been elucidated for specific drug-SCAR IM-ADRs such as Stevens-Johnson syndrome/toxic epidermal necrolysis, although the mechanisms by which carriage of a specific HLA allele is necessary but not sufficient for the development of many IM-ADRs is still being defined. SCAR management is complicated by substantial short- and long-term morbidity/mortality and the potential need to treat ongoing comorbid disease with related medications. Multidisciplinary specialist teams at experienced units should care for patients. In the setting of SCAR, patient outcomes as well as preventive, diagnostic, treatment, and management approaches are often not generalizable, but rather context specific, driven by population HLA-genetics, the pharmacology and genetic risk factors of the implicated drug, severity of underlying comorbid disease necessitating ongoing treatments, and cost considerations. In this review, we update the basic and clinical science of SCAR diagnosis and management.
大多数免疫介导的药物不良反应(IM-ADR)累及皮肤,且许多还伴有其他全身症状。严重皮肤药物不良反应(SCAR)是IM-ADR中一个罕见、可能危及生命且具有挑战性的亚组,具有多种临床表型、机制和致病药物。T细胞介导的免疫病理学是这些严重迟发性反应的核心,但效应细胞和细胞因子因临床表型而异。对于特定的药物-SCAR IM-ADR,如史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症,已阐明了与HLA基因的强关联,尽管特定HLA等位基因的携带对于许多IM-ADR的发生是必要但不充分的机制仍在研究中。SCAR的管理因大量的短期和长期发病率/死亡率以及可能需要使用相关药物治疗正在存在的合并症而变得复杂。经验丰富的单位的多学科专家团队应负责照顾患者。在SCAR的情况下,患者的预后以及预防、诊断、治疗和管理方法通常无法一概而论,而是因具体情况而异,受人群HLA遗传学、相关药物的药理学和遗传风险因素、需要持续治疗的潜在合并症的严重程度以及成本考虑等因素驱动。在本综述中,我们更新了SCAR诊断和管理的基础和临床科学。