Evidence map›Paper›PMID 41013380›Full record

ArticleBMC infectious diseases2025

Tracheobronchial infectious diseases in adult-onset immunodeficiency with anti-interferon-gamma autoantibodies.

Xiaona Liang, Nan Ma, Siqiao Liang, Xuemei Huang, Hanlin Liang, Siyao Wu, Yan Ning, Haiyan Pang, Ziyi Zhang, Ni Chen and 2 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Xiaona LiangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Nan MaDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Siqiao LiangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Xuemei HuangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Hanlin LiangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Siyao WuDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Yan NingDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Haiyan PangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Ziyi ZhangDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Ni ChenDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Limei HongDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China.
Zhiyi HeDepartment of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Guangxi Medical University, No. 6 Shuangyong Road, Nanning, Guangxi Zhuang Autonomous Region, 530021, China. zhiyi-river@163.com.

Funding

Central Leading Local Science and Technology Development Fund Project 2023ZYZX1021Guangxi Science and Technology Program 2023AB22055National Key R&D Program of China 2024YFC2309600
6 · The paper itself

Abstract

backgroundAnti-interferon (IFN)-γ autoantibodies predispose subjects to infections caused by opportunistic intracellular pathogens and lead to the involvement of multiple well-recognized organs, such as the lungs, skin, and lymph nodes. However, the clinical characteristics of tracheobronchial involvement remain unrecognized.

methodsA retrospective study was conducted between February 2016 and September 2024, enrolling patients with anti-IFN-γ autoantibodies who had documented evidence of tracheobronchial involvement. The clinical data were analyzed, including demographic information, clinical manifestations, laboratory results, chest computed tomography images, bronchoscopy findings, treatments, and clinical outcomes.

resultsA total of 33 patients were enrolled, with a mean age of 51.73 years old. The top five reported symptoms were cough, expectoration, fever, dyspnea, and fatigue. Laboratory tests showed elevated white blood cells, C-reactive protein, erythrocyte sedimentation rate, globulin, and immunoglobulin G. The detected pathogens included commonly reported opportunistic pathogens, such as Talaromyces marneffei (57.58%) and nontuberculous mycobacteria (42.42%), as well as the conventional pathogens typically found in patients without immunodeficiency diseases. Masses, nodules, and tracheobronchial stenosis were commonly seen on chest computed tomography scans and during bronchoscopy, directly indicating airway involvement. The predominant pathological results of the tracheobronchial lesions were chronic inflammation, with a small subset showing granuloma formation and abscess formation. Twenty-six patients (78.79%) achieved clinical improvement. Adverse events related to the therapeutic drug were reported in 30.3% of patients, with no life-threatening events.

conclusionsTracheobronchial lesions are characterized by masses, nodules, and tracheobronchial stenosis visualized during bronchoscopy, as well as inflammatory changes confirmed by pathologic examinations. Clinicians should be vigilant for tracheobronchial infections, particularly those caused by Talaromyces marneffei and nontuberculous mycobacteria. Pathogen-targeted therapy shows therapeutic benefits but requires close monitoring for drug-related toxicities.

Indexed as

AutoantibodiesImmunologic Deficiency SyndromesInterferon-gammaAdultAgedBronchoscopyFemaleHumansMaleMiddle AgedRetrospective StudiesTomography, X-Ray ComputedAutoantibodiesInterferon-gammaAnti-interferon-γ antibodyNontuberculous mycobacteriaTalaromyces MarneffeiTracheobronchial infections

Identifiers

PMID41013380
PMCPMC12465342

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.