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病毒导致呼吸道细菌继发感染的策略。

Viral strategies predisposing to respiratory bacterial superinfections.

机构信息

Pulmonary and Allergy Disease Unit, Department of Pediatrics, G. Gaslini University Hospital, Genoa, Italy.

Division of Pediatric Pulmonology, Miller School of Medicine, University of Miami, Miami, Florida.

出版信息

Pediatr Pulmonol. 2020 Apr;55(4):1061-1073. doi: 10.1002/ppul.24699. Epub 2020 Feb 21.

Abstract

Acute respiratory infections are amongst the leading causes of childhood morbidity and mortality globally. Viruses are the predominant cause of such infections, but mixed etiologies with bacteria has for decades raised the question of the interplay between them in causality and determination of the outcome of such infections. In this review, we examine recent microbiological, biochemical, and immunological advances that contribute to elucidating the mechanisms by which infections by specific viruses enable bacterial infections in the airway, and exacerbate them. We analyze specific domains in which viruses play such facilitating role including enhancement of bacterial adhesion by unmasking cryptic receptors and upregulation of adhesion proteins, disruption of tight junction integrity favoring paracellular transmigration of bacteria and loss of epithelial barrier integrity, increased availability of nutrient, such as mucins and iron, alteration of innate and adaptive immune responses, and disabling defense against bacteria, and lastly, changes in airway microbiome that render the lung more vulnerable to pathogens. Separate exhaustive analysis of each domain focuses on individuals with cystic fibrosis (CF), in whom viruses may play a key role in paving the way for the primary injury that leads to permanence of bacterial pathogens, viruses may then serve as triggers for "CF exacerbations"; these constituting the signature and ultimately the outcome determinants of these patients.

摘要

急性呼吸道感染是全球儿童发病率和死亡率的主要原因之一。病毒是此类感染的主要原因,但几十年来,细菌的混合病因引发了关于它们在因果关系和此类感染结果中的相互作用的问题。在这篇综述中,我们研究了最近在微生物学、生物化学和免疫学方面的进展,这些进展有助于阐明特定病毒感染如何使气道中的细菌感染得以发生并使其恶化的机制。我们分析了病毒发挥这种促进作用的特定领域,包括通过揭示隐藏的受体和上调粘附蛋白来增强细菌的粘附性、破坏紧密连接完整性以有利于细菌的旁细胞迁移和上皮屏障完整性的丧失、增加营养物质(如粘蛋白和铁)的可用性、改变先天和适应性免疫反应以及削弱对细菌的防御能力,最后,改变气道微生物组使肺部更容易受到病原体的侵害。对每个领域的单独详尽分析都集中在囊性纤维化 (CF) 患者身上,在这些患者中,病毒可能在为导致细菌病原体持续存在的主要损伤铺平道路方面发挥关键作用,病毒随后可能成为“CF 恶化”的触发因素;这些构成了这些患者的特征,最终也是决定结果的因素。

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