Cristina Ramos-Del Moral, Pablo Rodríguez Cortés, Marcos Navares-Gómez, Diana Campodónico, Susana Almenara de Riquer, Ana Barrios Blandino, Gina Mejía-Abril, Antía Gómez-Fernández, Olga Romero Sastre, Patricia Carles García, Francisco Abad-Santos
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We describe two cases of DRESS in a raltegravir-treated cohort and review the relevant literature.</p>\n </section>\n \n <section>\n \n <h3> Methodology</h3>\n \n <p>Medical records from Hospital Universitario de La Princesa (2008–2020) were retrospectively reviewed to identify patients genotyped for <i>HLA-B*53</i> who received raltegravir. Suspected DRESS cases were assessed using the RegiSCAR scoring system and Naranjo algorithm. A structured literature search was conducted to identify additional published cases.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Among 109 patients treated with raltegravir, three (2.8%) were <i>HLA-B*53</i> carriers. Two developed DRESS, while no events occurred in non-carriers. One presented with fever, rash, lymphadenopathy, hepatitis and HHV-6 reactivation (RegiSCAR 6). The second developed eosinophilia, rash and pulmonary symptoms (RegiSCAR 4). The third carrier remained asymptomatic. A continuity correction yielded a RR of 133.9. Nine additional cases were identified in the literature and summarized according to clinical features and <i>HLA-B*53</i> status.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Findings support a potential genetic predisposition involving <i>HLA-B*53:01</i> in raltegravir-induced DRESS. Screening in high-prevalence populations may help prevent severe reactions. 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引用次数: 0
摘要
雷替格拉韦是一种HIV整合酶抑制剂,虽然通常耐受性良好,但可能引起严重的反应,如嗜酸性粒细胞增加和全身症状(DRESS)。该综合征与药物代谢受损、病毒再激活和遗传因素(包括HLA-B*53:01)有关。我们在替地韦治疗的队列中描述了两例DRESS病例,并回顾了相关文献。方法:回顾性分析公主大学医院(Hospital Universitario de La Princesa) 2008-2020年的医疗记录,以确定接受雷替重力韦治疗的HLA-B*53基因型患者。使用RegiSCAR评分系统和Naranjo算法对疑似DRESS病例进行评估。进行结构化文献检索以确定其他已发表的病例。结果:109例患者中,有3例(2.8%)为HLA-B*53携带者。2例发生DRESS,非携带者无发生。1例表现为发热、皮疹、淋巴结病、肝炎和HHV-6再激活(RegiSCAR 6)。第二例出现嗜酸性粒细胞增多、皮疹和肺部症状(RegiSCAR 4)。第三名感染者无症状。连续性校正的风险比为133.9。根据临床特点及HLA-B*53状态对文献中新增9例进行总结。结论:研究结果支持与HLA-B*53:01有关的潜在遗传易感性。在高患病率人群中进行筛查可能有助于预防严重反应。进一步的研究应完善诊断和管理策略。
Association of HLA-B*53 With DRESS Syndrome in Patients Treated With Raltegravir: Two Case Reports and a Literature Review
Introduction
Raltegravir, an HIV integrase inhibitor, although generally well tolerated, may cause severe reactions such as drug reaction with eosinophilia and systemic symptoms (DRESS). This syndrome has been associated with impaired drug metabolism, viral reactivation and genetic factors including HLA-B*53:01. We describe two cases of DRESS in a raltegravir-treated cohort and review the relevant literature.
Methodology
Medical records from Hospital Universitario de La Princesa (2008–2020) were retrospectively reviewed to identify patients genotyped for HLA-B*53 who received raltegravir. Suspected DRESS cases were assessed using the RegiSCAR scoring system and Naranjo algorithm. A structured literature search was conducted to identify additional published cases.
Results
Among 109 patients treated with raltegravir, three (2.8%) were HLA-B*53 carriers. Two developed DRESS, while no events occurred in non-carriers. One presented with fever, rash, lymphadenopathy, hepatitis and HHV-6 reactivation (RegiSCAR 6). The second developed eosinophilia, rash and pulmonary symptoms (RegiSCAR 4). The third carrier remained asymptomatic. A continuity correction yielded a RR of 133.9. Nine additional cases were identified in the literature and summarized according to clinical features and HLA-B*53 status.
Conclusion
Findings support a potential genetic predisposition involving HLA-B*53:01 in raltegravir-induced DRESS. Screening in high-prevalence populations may help prevent severe reactions. Further research should refine diagnostic and management strategies.
期刊介绍:
Basic & Clinical Pharmacology and Toxicology is an independent journal, publishing original scientific research in all fields of toxicology, basic and clinical pharmacology. This includes experimental animal pharmacology and toxicology and molecular (-genetic), biochemical and cellular pharmacology and toxicology. It also includes all aspects of clinical pharmacology: pharmacokinetics, pharmacodynamics, therapeutic drug monitoring, drug/drug interactions, pharmacogenetics/-genomics, pharmacoepidemiology, pharmacovigilance, pharmacoeconomics, randomized controlled clinical trials and rational pharmacotherapy. For all compounds used in the studies, the chemical constitution and composition should be known, also for natural compounds.