Management of tuberculosis risk, screening and preventive therapy in patients with chronic autoimmune arthritis undergoing biotechnological and targeted immunosuppressive agents.

IF 5.9 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1494283
Andrea Picchianti-Diamanti, Alessandra Aiello, Chiara De Lorenzo, Giovanni Battista Migliori, Delia Goletti
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Abstract

Tuberculosis (TB) is the leading cause of death in the world from an infectious disease. Its etiologic agent, the Mycobacterium tuberculosis (Mtb), is a slow-growing bacterium that has coexisted in humans for thousands of years. According to the World Health Organization, 10.6 million new cases of TB and over 1 million deaths were reported in 2022. It is widely recognized that patients affected by chronic autoimmune arthritis such as rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS) have an increased incidence rate of TB disease compared to the general population. As conceivable, the risk is associated with age ≥65 years and is higher in endemic regions, but immunosuppressive therapy plays a pivotal role. Several systematic reviews have analysed the impact of anti-TNF-α agents on the risk of TB in patients with chronic autoimmune arthritis, as well as for other biologic disease-modifying immunosuppressive anti-rheumatic drugs (bDMARDs) such as rituximab, abatacept, tocilizumab, ustekinumab, and secukinumab. However, the data are less robust compared to those available with TNF-α inhibitors. Conversely, data on anti-IL23 agents and JAK inhibitors (JAK-i), which have been more recently introduced for the treatment of RA and PsA/AS, are limited. TB screening and preventive therapy are recommended in Mtb-infected patients undergoing bDMARDs and targeted synthetic (ts)DMARDs. In this review, we evaluate the current evidence from randomized clinical trials, long-term extension studies, and real-life studies regarding the risk of TB in patients with RA, PsA, and AS treated with bDMARDs and tsDMARDs. According to the current evidence, TNF-α inhibitors carry the greatest risk of TB progression among bDMARDs and tsDMARDs, such as JAK inhibitors and anti-IL-6R agents. The management of TB screening and the updated preventive therapy are reported.

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接受生物技术和靶向免疫抑制剂治疗的慢性自身免疫性关节炎患者的结核病风险管理、筛查和预防治疗
结核病(TB)是世界上导致死亡的主要传染病。它的病原结核分枝杆菌(Mtb)是一种生长缓慢的细菌,在人类体内共存了数千年。根据世界卫生组织的数据,2022年报告了1060万新发结核病病例和100多万人死亡。人们普遍认为,慢性自身免疫性关节炎如类风湿关节炎(RA)、银屑病关节炎(PsA)和强直性脊柱炎(as)患者的结核病发病率高于一般人群。可以想象,风险与年龄≥65岁相关,在流行地区风险更高,但免疫抑制治疗起关键作用。一些系统综述分析了抗tnf -α药物对慢性自身免疫性关节炎患者结核病风险的影响,以及其他生物疾病修饰性免疫抑制抗风湿药物(bDMARDs),如利妥昔单抗、阿巴接受、托珠单抗、乌斯特金单抗和塞金单抗。然而,与TNF-α抑制剂相比,这些数据不那么可靠。相反,最近用于治疗RA和PsA/AS的抗il - 23药物和JAK抑制剂(JAK- 1)的数据有限。建议在接受bDMARDs和靶向合成DMARDs治疗的mtb感染患者中进行结核病筛查和预防性治疗。在这篇综述中,我们评估了随机临床试验、长期扩展研究和现实生活研究中关于bDMARDs和tsDMARDs治疗的RA、PsA和AS患者结核病风险的现有证据。根据目前的证据,TNF-α抑制剂在bdmard和tsdmard中携带最大的结核病进展风险,如JAK抑制剂和抗il - 6r药物。报告了结核病筛查的管理和最新的预防治疗方法。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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