“The cytokine profiles of the inflammatory response in chronic granulomatous encephalitis caused by Mycobacterium tuberculosis do not influence the patient's clinical presentation"

IF 2.9 3区 医学 Q3 IMMUNOLOGY
Tuberculosis Pub Date : 2025-12-01 Epub Date: 2025-10-23 DOI:10.1016/j.tube.2025.102700
Alejandro Rivas-Castro , Itzel Rocío Manzano Espinosa , Diana Villa Sepúlveda , Eduardo Pablo Sánchez Martínez , José Alberto Choreño-Parra , Yaser Sánchez Gama , Ana Sofía Alonso Villaseñor , Fernando Daniel Argueta Muñoz , Erick Gómez Apo , Citlaltepetl Salinas-Lara , Carlos Sánchez-Garibay , Martha Lilia Tena Suck
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引用次数: 0

Abstract

Introduction

Central nervous system tuberculosis (CNS-TB) is the most lethal form of tuberculosis, characterized by severe clinical manifestations and distinctive histopathological changes. Although several cytokines are implicated in the immune response to Mycobacterium tuberculosis, their relationship with disease severity and histological alterations remains unclear. This study aimed to evaluate the associations between cytokine expression, histopathological changes, and clinical features in patients with CNS-TB.

Methods

We conducted a retrospective, observational, cross-sectional, descriptive study of 25 biopsies that fulfilled criteria for CNS-TB at the National Institute of Neurology and Neurosurgery “Manuel Velasco Suárez.” Cases were classified according to the Suzaan Marais criteria. Immunohistochemistry was performed to assess IL-1β, IL-4, IL-10, IL-17, IL-23, TNF-α, and IFN-γ expression in meningeal and parenchymal tissues.

Results

Strong expression of IL-1β, IL-17, IL-23, and TNF-α was observed in glial cells, vascular endothelial cells, and macrophages, particularly within inflammatory and vascular lesions.

Conclusions

Although no direct correlation was found between cytokine expression and clinical severity, the findings support a predominant pro-inflammatory response mediated by IL-1β, IL-17, IL-23, and TNF-α, associated with tissue and vascular damage. The elevated cytokine expression in foam cells suggests a potential role in local immune regulation in CNS-TB.
由结核分枝杆菌引起的慢性肉芽肿性脑炎炎症反应的细胞因子谱不影响患者的临床表现。
简介:中枢神经系统结核(CNS-TB)是最致命的结核形式,具有严重的临床表现和独特的组织病理学改变。尽管几种细胞因子与结核分枝杆菌的免疫应答有关,但它们与疾病严重程度和组织学改变的关系尚不清楚。本研究旨在评估CNS-TB患者细胞因子表达、组织病理学改变和临床特征之间的关系。方法:我们在国家神经病学和神经外科研究所“Manuel Velasco Suárez”对25例符合CNS-TB标准的活检进行了回顾性、观察性、横断面、描述性研究。根据Suzaan Marais标准对病例进行分类。采用免疫组化方法检测脑膜和实质组织中IL-1β、IL-4、IL-10、IL-17、IL-23、TNF-α和IFN-γ的表达。结果:IL-1β、IL-17、IL-23和TNF-α在神经胶质细胞、血管内皮细胞和巨噬细胞中表达强烈,尤其是在炎症和血管病变中。结论:虽然没有发现细胞因子表达与临床严重程度之间的直接相关性,但研究结果支持IL-1β, IL-17, IL-23和TNF-α介导的主要促炎反应与组织和血管损伤相关。泡沫细胞中细胞因子表达的升高提示CNS-TB局部免疫调节的潜在作用。
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来源期刊
Tuberculosis
Tuberculosis 医学-呼吸系统
CiteScore
4.60
自引率
3.10%
发文量
87
审稿时长
49 days
期刊介绍: Tuberculosis is a speciality journal focusing on basic experimental research on tuberculosis, notably on bacteriological, immunological and pathogenesis aspects of the disease. The journal publishes original research and reviews on the host response and immunology of tuberculosis and the molecular biology, genetics and physiology of the organism, however discourages submissions with a meta-analytical focus (for example, articles based on searches of published articles in public electronic databases, especially where there is lack of evidence of the personal involvement of authors in the generation of such material). We do not publish Clinical Case-Studies. Areas on which submissions are welcomed include: -Clinical TrialsDiagnostics- Antimicrobial resistance- Immunology- Leprosy- Microbiology, including microbial physiology- Molecular epidemiology- Non-tuberculous Mycobacteria- Pathogenesis- Pathology- Vaccine development. This Journal does not accept case-reports. The resurgence of interest in tuberculosis has accelerated the pace of relevant research and Tuberculosis has grown with it, as the only journal dedicated to experimental biomedical research in tuberculosis.
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