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肿瘤坏死因子 α 抑制剂治疗的各种炎症性疾病患者的球孢子菌病。

Coccidioidomycosis in patients with various inflammatory disorders treated with tumor necrosis factor α inhibitors.

机构信息

Department of Internal Medicine, Mayo Clinic, Scottsdale, Arizona.

Division of Infectious Diseases, Mayo Clinic Hospital, Phoenix, Arizona.

出版信息

Med Mycol. 2021 Jul 6;59(7):720-727. doi: 10.1093/mmy/myaa109.

Abstract

UNLABELLED

Coccidioides fungi are found primarily in the southwestern United States and are the cause of coccidioidomycosis. Tumor necrosis factor α inhibitors (TNFIs) are therapies for autoimmune and inflammatory conditions; their association with coccidioidomycosis is not well characterized. We aimed to determine the prevalence and characteristics of coccidioidomycosis among TNFI recipients with different inflammatory disorders at a tertiary care center. We retrospectively reviewed the electronic health records of patients at our institution from April 4, 2010 to December 17, 2017, who received TNFIs (infliximab, etanercept, adalimumab, certolizumab pegol, or golimumab) and had positive culture, pathologic, and/or serologic results for coccidioidomycosis. Among 1770 patients identified who received TNFIs, 49 (2.8%) had proven or probable coccidioidomycosis. Of these 49, 28 (57%) were men, 47 (96%) were White, and 42 (86%) had pulmonary coccidioidomycosis. The most common TNFIs used were adalimumab, infliximab, and etanercept. Coccidioidomycosis was identified in 25 of 794 patients with rheumatologic disorders (3.1%), 18 of 783 patients with inflammatory bowel disease (IBD) (2.3%), and six of 193 patients with dermatologic disorders (3.1%) (P = .34). There was no difference in coccidioidal infections among recipients of any particular TNFI agents. A minority of patients (7/49, 14%) had an extrapulmonary infection, and the majority of these (6/7) had IBD. Our study shows a low prevalence of coccidioidomycosis in TNFI recipients, even within the Coccidioides-endemic area. Persons with IBD were disproportionately represented among those with extrapulmonary coccidioidomycosis. Treatment with azoles was effective.

LAY SUMMARY

Among 1770 patients who received tumor necrosis factor α inhibitors, 49 (2.8%) had newly acquired coccidioidomycosis over a 7-year period. Dissemination occurred in 14.3%, but disproportionately among those with underlying inflammatory bowel disease. All patients recovered with medical management.

摘要

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球孢子菌真菌主要存在于美国西南部,是球孢子菌病的病因。肿瘤坏死因子 α 抑制剂(TNFIs)是治疗自身免疫和炎症性疾病的药物;它们与球孢子菌病的关系尚未得到很好的描述。我们旨在确定在一家三级保健中心,患有不同炎症性疾病的 TNFIs 接受者中球孢子菌病的患病率和特征。我们回顾性地审查了我院 2010 年 4 月 4 日至 2017 年 12 月 17 日期间接受 TNFIs(英夫利昔单抗、依那西普、阿达木单抗、certolizumab pegol 或戈利木单抗)治疗且球孢子菌病培养、病理和/或血清学阳性结果的患者的电子健康记录。在确定的 1770 名接受 TNFIs 治疗的患者中,有 49 名(2.8%)患有明确或可能的球孢子菌病。在这 49 名患者中,28 名(57%)为男性,47 名(96%)为白人,42 名(86%)患有肺球孢子菌病。最常用的 TNFIs 是阿达木单抗、英夫利昔单抗和依那西普。在 794 名患有风湿性疾病的患者中发现了 25 例(3.1%),在 783 名患有炎症性肠病(IBD)的患者中发现了 18 例(2.3%),在 193 名患有皮肤病的患者中发现了 6 例(3.1%)(P=.34)。在接受任何特定 TNFIs 药物的患者中,球孢子菌感染的发生率没有差异。少数患者(7/49,14%)有肺外感染,其中大多数(6/7)患有 IBD。我们的研究表明,在 TNFIs 接受者中,球孢子菌病的患病率较低,即使在球孢子菌流行地区也是如此。患有 IBD 的人在患有肺外球孢子菌病的人中所占比例不成比例。唑类药物治疗有效。

平铺直叙

在 7 年期间,1770 名接受肿瘤坏死因子 α 抑制剂治疗的患者中,有 49 名(2.8%)新患球孢子菌病。传播发生率为 14.3%,但在患有潜在炎症性肠病的患者中不成比例。所有患者均通过医疗管理康复。

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