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多种细胞内病原体感染伴眼病理改变与抗干扰素-γ自身抗体所致成人起病免疫缺陷相关:病例报告。

Multiple intracellular pathogen infections with ocular pathologies associated with adult-onset immunodeficiency due to anti-interferon-γ autoantibodies: a case report.

机构信息

The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

出版信息

BMC Infect Dis. 2024 Jan 12;24(1):78. doi: 10.1186/s12879-024-09003-x.

Abstract

BACKGROUND

Autoantibodies against interferon-γ (IFN-γ) can inhibit IFN-γ-dependent signal transducer and activator of transcription 1 phosphorylation and thus increase the risk of infection with intracellular pathogens, such as Talaromyces marneffei (TM), nontuberculous mycobacteria (NTMs), and Mycobacterium tuberculosis (TB). Here, we report a rare case of triple infection caused by TM, NTM, and TB in a human immunodeficiency virus-negative patient.

CASE PRESENTATION

A middle-aged female was admitted to our hospital after experiencing recurrent rash, cough, and expectoration for 4 months. She was successively diagnosed with NTM, TM, and TB infections without conventional immunosuppression-associated factors. However, after effective anti-infective treatment, the patient was confirmed to have allergic conjunctivitis and was successfully treated with corticosteroids and immunosuppressants. The most conspicuous characteristics were recurrent infection and immune disorders.

CONCLUSIONS

High-titer anti-IFN-γ autoantibodies are strongly associated with severe and disseminated infections, such as NTM, TM, and TB. It is characterized by persistently high degree of inflammation and high immunoglobin levels.

摘要

背景

针对干扰素-γ(IFN-γ)的自身抗体可抑制 IFN-γ 依赖性信号转导和转录激活子 1 的磷酸化,从而增加感染细胞内病原体(如马尔尼菲青霉(TM)、非结核分枝杆菌(NTM)和结核分枝杆菌(TB))的风险。在此,我们报告了一例人类免疫缺陷病毒阴性患者同时感染 TM、NTM 和 TB 的罕见病例。

病例介绍

一名中年女性因反复皮疹、咳嗽和咳痰 4 个月而入院。她先后被诊断为 NTM、TM 和 TB 感染,无常规免疫抑制相关因素。然而,在有效的抗感染治疗后,患者被确诊为过敏性结膜炎,并成功地接受了皮质类固醇和免疫抑制剂治疗。最显著的特征是反复感染和免疫紊乱。

结论

高滴度抗 IFN-γ 自身抗体与 NTM、TM 和 TB 等严重和播散性感染密切相关。其特征是持续高度炎症和高免疫球蛋白水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7edc/10785449/41cc7b78e978/12879_2024_9003_Fig1_HTML.jpg

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