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279 例接受生物治疗的银屑病患者的血清学结核干扰素释放试验结果。

Serial Quantiferon-TB Gold test results in 279 patients with psoriasis receiving biologic therapy.

机构信息

Hacettepe University, School of Medicine, Department of Dermatology and Venereology, Ankara, Turkey.

出版信息

Dermatol Ther. 2021 Jan;34(1):e14699. doi: 10.1111/dth.14699. Epub 2020 Dec 30.

DOI:10.1111/dth.14699
PMID:33368959
Abstract

The risk of active tuberculosis is still a concern in patients receiving biologics. To determine the risk of latent tuberculosis infection (LTBI) reactivation by Quantiferon-TB Gold (QFT) assay in psoriatic patients treated with biologics in 11 years' follow-up, along with chest radiography alterations. This retrospective study included 279 patients with plaque-type and/or pustular, or nail psoriasis who were treated with biologics, and had results for ≥2 LTBI tests. The QFT outcomes were defined according to the baseline and the follow-up QFT results; seroconversion as from negative to positive, seroreversion as from positive to negative, persistently seronegative as invariantly negative, persistently seropositive as invariantly positive, and other any result was accepted as indeterminate. Demographic features, the presence and the type of any chest X-ray abnormality was noted during the follow-up. Of 279 baseline QFT tests, the vast majority were negative (n = 193; 69%), with a less of positive (n = 86; 31%). Ten (5.2%) of 193 patients converted from negative to positive QFT status after starting biologic therapy (P < 0.001) during 11 years' follow-up. Although these 10 patients exhibited seroconversion of QFT from negative to positive, only one patient was diagnosed with active TB. There was no statistically significant difference among biologics as regards with QFT seroconversion risk (P = .09). This study showed that 5.2% of patients showed seroconversion. Annual QFT testing remains a necessary and mandatory tool to prevent further TB reactivation in psoriasis patients taking biologic therapy although only one patient was diagnosed with active TB in this cohort.

摘要

在接受生物制剂治疗的患者中,活动性结核病的风险仍然令人担忧。为了确定在 11 年的随访中,接受生物制剂治疗的银屑病患者中,用 Quantiferon-TB Gold(QFT)检测潜伏性结核感染(LTBI)再激活的风险,以及胸部放射学改变。这项回顾性研究包括 279 名斑块型和/或脓疱型或指甲银屑病患者,他们接受了生物制剂治疗,并且有≥2 次 LTBI 检测结果。QFT 结果根据基线和随访 QFT 结果定义;血清转换为从阴性转为阳性,血清学逆转从阳性转为阴性,持续阴性为不变阴性,持续阳性为不变阳性,其他任何结果均被认为不确定。在随访期间记录了人口统计学特征、任何胸部 X 射线异常的存在和类型。在 279 次基线 QFT 检测中,绝大多数为阴性(n = 193;69%),阳性较少(n = 86;31%)。在 11 年的随访中,10 名(5.2%)接受生物治疗的患者从阴性 QFT 状态转为阳性 QFT 状态(P < 0.001)。尽管这 10 名患者的 QFT 从阴性转为阳性,但只有一名患者被诊断为活动性结核病。在 QFT 血清转化率方面,生物制剂之间无统计学差异(P =.09)。本研究显示,5.2%的患者出现血清转换。尽管在这组患者中只有一名患者被诊断为活动性结核病,但每年进行 QFT 检测仍然是预防接受生物治疗的银屑病患者进一步结核再激活的必要和强制性工具。

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引用本文的文献

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