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在接受抗 TNF-α 治疗前对银屑病患者进行结核风险分层。

Tuberculosis Risk Stratification of Psoriatic Patients Before Anti-TNF-α Treatment.

机构信息

Dermatology Department, Hôpital Erasme, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Laboratory of Vaccinology and Mucosal Immunity, Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

出版信息

Front Immunol. 2021 Jun 3;12:672894. doi: 10.3389/fimmu.2021.672894. eCollection 2021.

Abstract

Psoriasis is a skin inflammatory condition for which significant progress has been made in its management by the use of targeted biological drugs. Detection of latent infection (LTBI) is mandatory before starting biotherapy that is associated with reactivation risk. Together with evaluation of TB risk factors and chest radiographs, tuberculin skin tests (TST) and/or blood interferon-γ-release assays (IGRA), like the QuantiFERON (QFT), are usually performed to diagnose infection. Using this approach, 14/49 psoriatic patients prospectively included in this study were identified as LTBI (14 TST, induration size ≥ 10mm, 8 QFT), and 7/14 received prophylactic anti-TB treatment, the other 7 reporting past-treatment. As the specificity and sensitivity of these tests were challenged, we evaluated the added value of an IGRA in response to a mycobacterial antigen associated with latency, the heparin-binding haemagglutinin (HBHA). All but one TST patient had a positive HBHA-IGRA, indicating higher sensitivity than the QFT. The HBHA-IGRA was also positive for 12/35 TSTQFT patients. Measurement for 15 psoriatic patients (12 with HBHA-IGRA) of 8 chemokines in addition to IFN-γ revealed a broad array of HBHA-induced chemokines for TSTQFT and TSTQFT patients, compared to a more restricted pattern for TSTQFT patients. This allowed us to define subgroups within psoriatic patients characterized by different immune responses to antigens that may be associated to different risk levels of reactivation of the infection. This approach may help in prioritizing patients who should receive prophylactic anti-TB treatment before starting biotherapies in order to reduce their number.

摘要

银屑病是一种皮肤炎症性疾病,通过使用靶向生物药物,其治疗已取得显著进展。在开始生物治疗之前,必须检测潜伏性感染(LTBI),因为生物治疗与再激活风险相关。除了评估结核病危险因素和胸部 X 光片外,结核菌素皮肤试验(TST)和/或干扰素-γ释放试验(IGRA),如 QuantiFERON(QFT),通常用于诊断感染。采用这种方法,在这项前瞻性研究中,14/49 例银屑病患者被确定为 LTBI(14 例 TST 硬结直径≥10mm,8 例 QFT),其中 7 例接受了预防性抗结核治疗,另外 7 例曾接受过治疗。由于这些检测的特异性和敏感性受到了挑战,我们评估了一种针对潜伏相关分枝杆菌抗原——肝素结合血凝素(HBHA)的 IGRA 的附加价值。除了一个 TST 患者外,所有患者的 HBHA-IGRA 均为阳性,表明其敏感性高于 QFT。12/35 例 TSTQFT 患者的 HBHA-IGRA 也为阳性。对 15 例银屑病患者(12 例 HBHA-IGRA)进行了 8 种趋化因子的检测,结果显示,与 TSTQFT 患者相比,TSTQFT 和 TSTQFT 患者的 HBHA-IGRA 产生的趋化因子范围更广,而 TSTQFT 患者的趋化因子模式则更为局限。这使我们能够根据对 抗原的不同免疫反应来定义银屑病患者的亚组,这些反应可能与感染再激活的风险水平不同相关。这种方法可能有助于确定哪些患者需要在开始生物治疗之前接受预防性抗结核治疗,从而减少治疗人数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e7e/8209474/92a8f79fc05a/fimmu-12-672894-g001.jpg

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