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介导卡介苗接种异源效应的免疫机制:一项系统综述

Immune mechanisms mediating the heterologous effects of BCG vaccination: a systematic review.

作者信息

Torracinta Louis, Gogichadze Nino, Tanner Rachel

机构信息

Medical Sciences Division, University of Oxford, Oxford, United Kingdom.

Experimental Tuberculosis Unit, Microbiology Department, Germans Trias i Pujol Research Institute (IGTP) and Hospital (HUGTIP), Badalona, Spain.

出版信息

Front Immunol. 2025 May 19;16:1567111. doi: 10.3389/fimmu.2025.1567111. eCollection 2025.

Abstract

INTRODUCTION

BCG vaccination can have heterologous or non-specific effects (NSE) that confer resistance against pathogens other than its target Mycobacterium tuberculosis, but the underlying mechanisms are not fully understood.

METHODS

We conducted a systematic review synthesising existing literature on immune mechanisms mediating the heterologous/NSE of BCG. Searches were conducted using MEDLINE and Scopus.

RESULTS

1032 original records were identified, of which 67 were deemed eligible. Several potentially relevant immune pathways were identified, although there may be variation by pathogen. Recent studies have focused on trained immunity whereby innate cells, or the hematopoietic stem and progenitor cells from which they are derived, undergo epigenetic and metabolic reprogramming allowing them to respond more effectively to antigen exposures unrelated to the original stimulus. However, other processes such as granulopoiesis and cross-reactive adaptive immunity may also play a role. Heterologous immunity and NSEs may be influenced by several endogenous and exogenous variables.

DISCUSSION

We discuss the quality of available data, the importance of understanding mechanisms of heterologous protection, and its implications for vaccination strategies.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/PROSPERO/view/CRD42023400375, identifier CRD42023400375.

摘要

引言

卡介苗接种可产生异源或非特异性效应(NSE),从而对其目标病原体结核分枝杆菌以外的病原体产生抗性,但其潜在机制尚未完全明确。

方法

我们进行了一项系统综述,综合了关于介导卡介苗异源/非特异性效应的免疫机制的现有文献。使用MEDLINE和Scopus进行检索。

结果

共识别出1032条原始记录,其中67条被认为符合要求。确定了几种潜在相关的免疫途径,尽管不同病原体可能存在差异。最近的研究集中在训练免疫上,即先天细胞或其来源的造血干细胞和祖细胞经历表观遗传和代谢重编程,使其能够更有效地对抗与原始刺激无关的抗原暴露作出反应。然而,其他过程如粒细胞生成和交叉反应性适应性免疫也可能起作用。异源免疫和非特异性效应可能受多种内源性和外源性变量的影响。

讨论

我们讨论了现有数据的质量、理解异源保护机制的重要性及其对疫苗接种策略的影响。

系统综述注册

https://www.crd.york.ac.uk/PROSPERO/view/CRD42023400375,标识符CRD42023400375。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca21/12127298/683bdbbf0b63/fimmu-16-1567111-g001.jpg

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