Department of Internal Medicine, Radboud University Medical Centre, Nijmegen, the Netherlands.
Department of Internal Medicine, Radboud University Medical Centre, Nijmegen, the Netherlands.
Clin Microbiol Infect. 2019 Dec;25(12):1473-1478. doi: 10.1016/j.cmi.2019.04.020. Epub 2019 May 2.
Some strains of Bacillus Calmette-Guérin (BCG) vaccine not only confer protection against disseminated forms of tuberculosis, but also reduce all-cause mortality by the induction of protection against infections with non-related pathogens.
We review evidence for non-specific protection induced by BCG vaccination against viral infections, discuss possible mechanisms of action, and summarize implications for vaccination policies and vaccine discovery.
Relevant studies retrieved from PubMed and clinicaltrials.gov.
Numerous epidemiological, clinical and immunological studies demonstrate that BCG vaccination impacts the immune response to subsequent infections, resulting in reduced morbidity and mortality. Important lines of evidence indicating that BCG protects against viral pathogens comes from experimental studies in mice showing that BCG offers protection against various DNA and RNA viruses, including herpes and influenza viruses. Recently, the effect of BCG on an experimental viral infection in humans has been demonstrated. These effects are thought to be mediated via the induction of innate immune memory and heterologous lymphocyte activation, resulting in enhanced cytokine production, macrophage activity, T-cell responses and antibody titres.
The discovery of innate immune memory has greatly improved our understanding of the mechanisms underlying the non-specific effects induced by BCG vaccination. However, a full understanding of the molecular mechanisms that underlie this phenomenon is still evolving. By identifying the factors that impact the non-specific effects of BCG, we will take an important step towards novel therapeutic options and vaccination strategies, which might lead to a reduction in severe morbidity and mortality associated with viral infections.
某些卡介苗(BCG)菌株不仅能预防结核分枝杆菌的全身感染,还能通过诱导对非相关病原体的感染产生保护作用,从而降低全因死亡率。
我们综述了卡介苗接种诱导非特异性保护作用预防病毒感染的证据,讨论了可能的作用机制,并总结了对疫苗接种政策和疫苗发现的影响。
从 PubMed 和 clinicaltrials.gov 检索到的相关研究。
大量的流行病学、临床和免疫学研究表明,BCG 疫苗接种会影响对随后感染的免疫反应,从而降低发病率和死亡率。重要的证据表明 BCG 可以保护免受病毒病原体的侵害,这来自于实验研究,该研究表明 BCG 可以预防各种 DNA 和 RNA 病毒,包括疱疹病毒和流感病毒。最近,已经在人体的实验性病毒感染中证明了 BCG 的作用。这些作用被认为是通过诱导先天免疫记忆和异源淋巴细胞激活来介导的,从而导致细胞因子产生、巨噬细胞活性、T 细胞反应和抗体滴度增强。
先天免疫记忆的发现极大地提高了我们对 BCG 接种诱导非特异性效应的机制的理解。然而,对这种现象背后的分子机制的全面理解仍在不断发展。通过确定影响 BCG 非特异性效应的因素,我们将朝着新的治疗选择和疫苗接种策略迈出重要一步,这可能会减少与病毒感染相关的严重发病率和死亡率。