Infection risk of targeted synthetic drugs used in immune-mediated inflammatory diseases

P. García, Amaya Arrondo, M. D. De Miguel
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Abstract

OBJECTIVE To review the available evidence concerning the infectious risks related to the targeted synthetic drugs used in immune-mediated inflammatory diseases and the measures for preventing infections in this type of disease. MATERIAL AND METHODS Targeted synthetic drugs with an indication in immune-mediated inflammatory diseases, including rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, juvenile idiopathic arthritis, inflammatory bowel disease, psoriasis and atopic dermatitis, were selected. The summary of product information for these drugs were consulted and a search carried out in Pubmed, reviewing the most relevant articles and clinical guidelines. RESULTS AND CONCLUSIONS Patients with immune-mediated inflammatory diseases present a higher risk of developing infections compared with the general population, partly due to immunosuppressive therapy. The infection risk associated with these treatments depends on the mechanism of action. There is no evidence for an increased risk of serious infections associated with apremilast use. Therefore, prior to initiating therapy with apremilast, no type of test other than clinical monitoring of the disease needs to be performed. Treatment with JAK inhibitors has been associated with an increase in infection risk, including reactivation of tuberculosis, herpes zoster and hepatitis B, among other infections. The vaccination status must be evaluated, a screening for infection with hepatitis B or latent tuberculosis performed, and an active systemic or local infection ruled out before starting treatment with JAK inhibitors. The inactivated vaccines recommended for patients being treated with JAK inhibitors are pneumococcus, influenza, hepatitis A, hepatitis B, herpes zoster and SARS-CoV-2. Attenuated live vaccines are contraindicated in these patients. Insufficient data are available to demonstrate that apremilast or JAK inhibitors increase the risk of COVID-19 infection and its complications. It is important that both healthcare professionals and patients are aware of the infection-prevention measures and recognise the signs and symptoms of infection before and during treatment with these drugs. KEY WORDS Targeted synthetic drugs, immune-mediated diseases, infection risk, herpes zoster, tuberculosis, vaccination
靶向合成药物用于免疫介导炎性疾病的感染风险
目的综述免疫介导性炎症性疾病中靶向合成药物感染风险的现有证据及预防此类疾病感染的措施。材料和方法选择免疫介导的炎症性疾病(包括类风湿关节炎、银屑病关节炎、强直性脊柱炎、青少年特发性关节炎、炎症性肠病、银屑病和特应性皮炎)适应症的靶向合成药物。我们查阅了这些药物的产品信息摘要,并在Pubmed上进行了搜索,审查了最相关的文章和临床指南。结果和结论:与普通人群相比,免疫介导的炎症性疾病患者发生感染的风险更高,部分原因是免疫抑制治疗。与这些治疗相关的感染风险取决于作用机制。没有证据表明使用阿普米司特会增加严重感染的风险。因此,在开始阿普米司特治疗之前,除了临床监测疾病外,不需要进行任何类型的测试。使用JAK抑制剂治疗与感染风险增加相关,包括结核病、带状疱疹和乙型肝炎等感染的再激活。在开始使用JAK抑制剂治疗之前,必须评估疫苗接种状况,筛查乙型肝炎或潜伏性结核病感染,并排除活动性全身或局部感染。建议接受JAK抑制剂治疗的患者使用的灭活疫苗为肺炎球菌、流感、甲型肝炎、乙型肝炎、带状疱疹和SARS-CoV-2。这些患者禁用减毒活疫苗。没有足够的数据证明阿普米司特或JAK抑制剂会增加COVID-19感染及其并发症的风险。重要的是,保健专业人员和患者都要了解预防感染的措施,并在使用这些药物治疗之前和期间认识到感染的体征和症状。【关键词】靶向合成药物,免疫介导性疾病,感染风险,带状疱疹,结核病,疫苗接种
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