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2
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Hydrochlorothizide-induced acute generalised exanthematous pustulosis presenting with bilateral periorbital impetigo.氢氯噻嗪诱发的急性泛发性脓疱性皮病伴双侧眶周脓疱疮。
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本文引用的文献

1
Specific HLA types are associated with antiepileptic drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese subjects.特定的人类白细胞抗原类型与日本患者的抗癫痫药物诱导的史蒂文斯-约翰逊综合征和中毒性表皮坏死松解症相关。
Pharmacogenomics. 2013 Nov;14(15):1821-31. doi: 10.2217/pgs.13.180.
2
HLA-B*13:01 and the dapsone hypersensitivity syndrome.HLA-B*13:01 与氨苯砜超敏反应综合征。
N Engl J Med. 2013 Oct 24;369(17):1620-8. doi: 10.1056/NEJMoa1213096.
3
"Cutaneous adverse drug reactions" are not always drug-induced.“皮肤不良反应”并不总是由药物引起的。
Eur J Dermatol. 2013 Jul-Aug;23(4):439-42. doi: 10.1684/ejd.2013.2055.
4
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome secondary to antituberculosis drugs and associated with human herpes virus-7 (HHV-7).抗结核药物继发的伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)综合征,并与人疱疹病毒7型(HHV-7)相关。
BMJ Case Rep. 2013 Jul 31;2013:bcr2013010348. doi: 10.1136/bcr-2013-010348.
5
Relationship between the HLA-B*1502 allele and carbamazepine-induced Stevens-Johnson syndrome and toxic epidermal necrolysis: a systematic review and meta-analysis.HLA-B*1502 等位基因与卡马西平诱导的 Stevens-Johnson 综合征和中毒性表皮坏死松解症的关系:系统评价和荟萃分析。
JAMA Dermatol. 2013 Sep;149(9):1025-32. doi: 10.1001/jamadermatol.2013.4114.
6
HLA alleles influence the clinical signature of amoxicillin-clavulanate hepatotoxicity.HLA 等位基因影响阿莫西林克拉维酸钾肝毒性的临床特征。
PLoS One. 2013 Jul 9;8(7):e68111. doi: 10.1371/journal.pone.0068111. Print 2013.
7
Allopurinol hypersensitivity: a systematic review of all published cases, 1950-2012.别嘌醇过敏反应:1950 年至 2012 年所有已发表病例的系统回顾。
Drug Saf. 2013 Oct;36(10):953-80. doi: 10.1007/s40264-013-0084-0.
8
Systemic involvement of acute generalized exanthematous pustulosis: a retrospective study on 58 patients.急性泛发性发疹性脓疱病的系统受累:58 例回顾性研究。
Br J Dermatol. 2013 Dec;169(6):1223-32. doi: 10.1111/bjd.12502.
9
The association between oxcarbazepine-induced maculopapular eruption and HLA-B alleles in a northern Han Chinese population.在一个北方汉族人群中,奥卡西平诱导的斑丘疹性发疹与 HLA-B 等位基因之间的关联。
BMC Neurol. 2013 Jul 8;13:75. doi: 10.1186/1471-2377-13-75.
10
HLA-B*57:01(+) abacavir-naive individuals have specific T cells but no patch test reactivity.HLA - B*57:01阳性且未使用过阿巴卡韦的个体有特定的T细胞,但无斑贴试验反应性。
J Allergy Clin Immunol. 2013 Sep;132(3):756-758. doi: 10.1016/j.jaci.2013.04.013. Epub 2013 May 23.

发热、皮疹和全身症状:了解病毒和 HLA 在严重皮肤药物过敏中的作用。

Fever, rash, and systemic symptoms: understanding the role of virus and HLA in severe cutaneous drug allergy.

机构信息

Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia.

Institute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia; Vanderbilt University School of Medicine, Nashville, Tenn.

出版信息

J Allergy Clin Immunol Pract. 2014 Jan-Feb;2(1):21-33. doi: 10.1016/j.jaip.2013.11.005.

DOI:10.1016/j.jaip.2013.11.005
PMID:24565765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4020624/
Abstract

Drug hypersensitivity syndromes such as abacavir hypersensitivity and the severe cutaneous adverse drug reactions have been associated with significant short- and long-term morbidity and mortality. More recently, these immunologically mediated and previously unpredictable diseases have been shown to be associated with primarily class I but also class II HLA alleles. The case of the association of HLA-B*57:01 and abacavir hypersensitivity has created a translational roadmap for how this knowledge can be used in the clinic to prevent severe reactions. Although many hurdles exist to the widespread translation of such HLA screening approaches, our understanding of how drugs interact with the major histocompatibility complex has contributed to the discovery of new models that have provided considerable insights into the immunopathogenesis of severe cutaneous adverse drug reactions and other T-cell-mediated drug hypersensitivity syndromes. Future translation of this knowledge will facilitate the development of preclinical toxicity screening to significantly improve efficacy and safety of drug development and design.

摘要

药物超敏反应综合征,如阿巴卡韦超敏反应和严重皮肤不良反应,与显著的短期和长期发病率和死亡率相关。最近,这些免疫介导的、以前不可预测的疾病已被证明与主要的 I 类但也有 II 类 HLA 等位基因相关。HLA-B*57:01 与阿巴卡韦超敏反应的关联为如何将这一知识应用于临床以预防严重反应提供了一个转化途径。尽管 HLA 筛选方法的广泛转化存在许多障碍,但我们对药物如何与主要组织相容性复合体相互作用的理解,有助于发现新的模型,这些模型为严重皮肤不良反应和其他 T 细胞介导的药物超敏反应综合征的免疫发病机制提供了重要的见解。这方面知识的未来转化将促进临床前毒性筛选的发展,从而显著提高药物开发和设计的疗效和安全性。