Hepatitis B Virus Reactivation in Patients with Psoriasis on Biologic Therapies: A Retrospective Study

Sinan Ozcelik, Fatma Kılı
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引用次数: 4

Abstract

Background: There are limited data on the safety of biological therapies in psoriasis patients with hepatitis B virus (HBV) infection in the literature, and are still ongoing controversies about HBV reactivation in patients treated with biologics for psoriasis. Aims: This was aimed to investigate the demographic, clinical, and laboratory characteristics of the patients with HBV seropositive receiving biological treatment for psoriasis. Study Design: This was a retrospective observational study. Materials and Methods: Ninety-seven patients with psoriasis treated with biologics in the outpatient clinic were evaluated retrospectively. Of these, 16 patients with HBV seropositive were included in the study. Patients with positive HBV serology were divided into three groups as chronic HBV infection, past HBV infection, and isolated core antibody positivity (HBV core-specific antibody [HBcAb]). The demographic, clinical, and laboratory characteristics of the patients were obtained from the records. Results: Of the patients, 5 patients were female (31.2%), and 11 were male (68.8%). The mean age of the patients was 55.81 ± 11.05. Thirteen of the patients had past HBV infection, three had isolated HBcAb positive. Infliximab (n = 13) was the most common biologic agent used, followed by adalimumab (n = 6), secukinumab (n = 4), ustekinumab (n = 2), and etanercept (n = 2). The mean duration of treatment was 3.59 ± 2.76 years. The HBV reactivation occurred in only one patient with past HBV infection receiving infliximab (6.2%). Conclusion: It remains unclear how exactly the biologic drugs for psoriasis impact viral reactivation. For the safe use of biological agents in psoriasis patients with HBV seropositive, screening tests must be performed with a triple serology, including HBV surface antigen, HBV surface-specific antibody, and HBcAb. The patients who have positive HBV serology must be monitored closely with reactivation markers and receive antiviral prophylaxis if they are at moderate-to-high risk of HBV reactivation.
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银屑病患者乙肝病毒在生物治疗中的再激活:一项回顾性研究
背景:文献中关于生物疗法治疗银屑病合并乙型肝炎病毒(HBV)感染患者安全性的数据有限,银屑病生物制剂治疗患者HBV再激活的问题仍存在争议。目的:研究接受银屑病生物治疗的HBV血清阳性患者的人口学、临床和实验室特征。研究设计:这是一项回顾性观察性研究。材料与方法:回顾性分析97例门诊用生物制剂治疗银屑病的临床疗效。其中,16例HBV血清阳性患者被纳入研究。将HBV血清学阳性患者分为慢性HBV感染组、既往HBV感染组和分离核心抗体阳性组(HBV核心特异性抗体[HBcAb])。患者的人口学、临床和实验室特征从记录中获得。结果:女性5例(31.2%),男性11例(68.8%)。患者平均年龄55.81±11.05岁。13例既往HBV感染,3例分离HBcAb阳性。英夫利昔单抗(n = 13)是最常用的生物制剂,其次是阿达木单抗(n = 6)、secukinumab (n = 4)、ustekinumab (n = 2)和依那西普(n = 2)。平均治疗时间为3.59±2.76年。接受英夫利昔单抗治疗的既往HBV感染患者中只有1例(6.2%)发生HBV再激活。结论:治疗银屑病的生物药物究竟如何影响病毒再激活尚不清楚。为了在HBV血清阳性银屑病患者中安全使用生物制剂,必须进行三重血清学筛查试验,包括HBV表面抗原、HBV表面特异性抗体和HBcAb。HBV血清学阳性的患者必须密切监测再激活标志物,如果他们有HBV再激活的中至高风险,则必须接受抗病毒预防。
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13
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