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Cyclosporine treatment for Stevens-Johnson syndrome/toxic epidermal necrolysis: Retrospective analysis of a cohort treated in a specialized referral center.环孢素治疗 Stevens-Johnson 综合征/中毒性表皮坏死松解症:在专门转诊中心治疗的队列的回顾性分析。
J Am Acad Dermatol. 2017 Jan;76(1):106-113. doi: 10.1016/j.jaad.2016.07.048. Epub 2016 Oct 4.
2
Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.与抗甲状腺药物诱导的粒细胞缺乏症相关的遗传变异:一项在欧洲人群中的全基因组关联研究。
Lancet Diabetes Endocrinol. 2016 Jun;4(6):507-16. doi: 10.1016/S2213-8587(16)00113-3. Epub 2016 May 3.
3
Diagnostic patch testing following tuberculosis-associated cutaneous adverse drug reactions induces systemic reactions in HIV-infected persons.诊断性斑贴试验可诱发 HIV 感染者出现结核相关性皮肤药物不良反应的全身性反应。
Br J Dermatol. 2016 Jul;175(1):150-6. doi: 10.1111/bjd.14492. Epub 2016 May 26.
4
HLA-B*38:02:01 predicts carbimazole/methimazole-induced agranulocytosis.HLA - B*38:02:01可预测卡比马唑/甲巯咪唑诱发的粒细胞缺乏症。
Clin Pharmacol Ther. 2016 May;99(5):555-61. doi: 10.1002/cpt.309. Epub 2016 Jan 12.
5
Drug hypersensitivity in children: report from the pediatric task force of the EAACI Drug Allergy Interest Group.儿童药物过敏反应:来自 EAACI 药物过敏兴趣小组儿科工作组的报告。
Allergy. 2016 Feb;71(2):149-61. doi: 10.1111/all.12774. Epub 2015 Nov 17.
6
Allopurinol Desensitization: A Fast or Slow Protocol?别嘌醇脱敏:快速方案还是慢速方案?
J Investig Allergol Clin Immunol. 2015;25(4):295-7.
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Classifying ADRs--does dose matter?药物不良反应的分类——剂量重要吗?
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8
Pharmacogenetics as a tool to tailor antiretroviral therapy: A review.药物遗传学作为定制抗逆转录病毒疗法的工具:综述
World J Virol. 2015 Aug 12;4(3):198-208. doi: 10.5501/wjv.v4.i3.198.
9
Stevens Johnson Syndrome and Toxic Epidermal Necrolysis: Maternal and Foetal Outcomes in Twenty-Two Consecutive Pregnant HIV Infected Women.史蒂文斯-约翰逊综合征和中毒性表皮坏死松解症:22例连续妊娠的HIV感染孕妇的母婴结局
PLoS One. 2015 Aug 12;10(8):e0135501. doi: 10.1371/journal.pone.0135501. eCollection 2015.
10
Evolving models of the immunopathogenesis of T cell-mediated drug allergy: The role of host, pathogens, and drug response.T细胞介导的药物过敏免疫发病机制的演变模型:宿主、病原体和药物反应的作用。
J Allergy Clin Immunol. 2015 Aug;136(2):219-34; quiz 235. doi: 10.1016/j.jaci.2015.05.050.

药物引起的严重迟发性皮肤和全身反应:当前实践科学与艺术的全球视角

Severe Delayed Cutaneous and Systemic Reactions to Drugs: A Global Perspective on the Science and Art of Current Practice.

作者信息

Peter Jonathan Grant, Lehloenya Rannakoe, Dlamini Sipho, Risma Kimberly, White Katie D, Konvinse Katherine C, Phillips Elizabeth J

机构信息

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.

出版信息

J Allergy Clin Immunol Pract. 2017 May-Jun;5(3):547-563. doi: 10.1016/j.jaip.2017.01.025.

DOI:10.1016/j.jaip.2017.01.025
PMID:28483310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5424615/
Abstract

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.

摘要

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。