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播散性隐球菌病和抗粒细胞-巨噬细胞集落刺激因子自身抗体:一个被低估的关联。

Disseminated cryptococcosis and anti-granulocyte-macrophage colony-stimulating factor autoantibodies: An underappreciated association.

机构信息

Department of Infectious Diseases, Infection Control, and Employee Health, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

National Institute of Allergy and Infectious Diseases, Bethesda, MD, USA.

出版信息

Mycoses. 2021 Jun;64(6):576-582. doi: 10.1111/myc.13247. Epub 2021 Feb 5.

Abstract

The development of disseminated cryptococcosis has historically occurred in patients living with advanced human immunodeficiency virus or other immunosuppressive conditions affecting T-cell function. Recently, patients with anti-cytokine neutralising autoantibodies have been recognised to be at risk for disseminated infections by opportunistic intracellular pathogens, including Cryptococcus species. Herein, we present a previously healthy 26-year-old man who was evaluated with disseminated cryptococcosis involving the bone, lung, mediastinum and brain. The patient's serum cryptococcal antigen titres were >1:1,100,000, and evaluation for an underlying immunodeficiency revealed high titres for anti-granulocyte-macrophage colony-stimulating factor (GM-CSF) autoantibodies. We also review the literature of all published cases of disseminated cryptococcosis associated with the presence of anti-GM-CSF autoantibodies. Clinicians should have a heightened awareness of anti-cytokine autoantibodies in patients without a known immunodeficiency and development disseminated infections by opportunistic intracellular pathogens.

摘要

播散性隐球菌病的发展历史上发生在人类免疫缺陷病毒(HIV)晚期或其他影响 T 细胞功能的免疫抑制状态的患者中。最近,人们已经认识到,具有抗细胞因子中和自身抗体的患者存在机会性细胞内病原体(包括隐球菌属)播散感染的风险。在此,我们介绍了一位以前健康的 26 岁男性,他因涉及骨骼、肺部、纵隔和大脑的播散性隐球菌病而接受了评估。患者的血清隐球菌抗原滴度>1:1,100,000,对潜在免疫缺陷的评估显示抗粒细胞-巨噬细胞集落刺激因子(GM-CSF)自身抗体的高滴度。我们还回顾了所有已发表的播散性隐球菌病与抗 GM-CSF 自身抗体存在相关的病例文献。临床医生应该对没有已知免疫缺陷的患者中存在的抗细胞因子自身抗体以及机会性细胞内病原体播散感染有更高的认识。

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