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应对产肠毒素疫苗开发面临的挑战。

Confronting challenges to enterotoxigenic vaccine development.

作者信息

Fleckenstein James M

机构信息

Department of Medicine, Division of Infectious Diseases, Washington University in Saint Louis, School of Medicine, Saint Louis, Missouri, USA.

Medicine Service, Infectious Diseases, John Cochran Saint Louis Veterans Affairs Health Care System, Saint Louis, Missouri, USA.

出版信息

Front Trop Dis. 2021;2. doi: 10.3389/fitd.2021.709907. Epub 2021 Sep 24.

DOI:10.3389/fitd.2021.709907
PMID:35937717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9355458/
Abstract

The enterotoxigenic (ETEC) are a diverse and genetically plastic pathologic variant (pathovar) of defined by their production of heat-labile (LT) and heat-stable (ST) enterotoxins. These pathogens, which came to recognition more than four decades ago in patients presenting with severe cholera-like diarrhea, are now known to cause hundreds of millions of cases of symptomatic infection annually. Children in low-middle income regions of the world lacking access to clean water and basic sanitation are disproportionately affected by ETEC. In addition to acute diarrheal morbidity, these pathogens remain a significant cause of mortality in children under the age of five years and have also been linked repeatedly to sequelae of childhood malnutrition and growth stunting. Vaccines that could prevent ETEC infections therefore remain a high priority. Despite several decades of effort, a licensed vaccine that protects against the breadth of these pathogens remains an aspirational goal, and the underlying genetic plasticity of has posed a fundamental challenge to development of a vaccine that can encompass the complete antigenic spectrum of ETEC. Nevertheless, novel strategies that include toxoids, a more complete understanding of ETEC molecular pathogenesis, structural details of target immunogens, and the discovery of more highly conserved antigens essential for virulence should accelerate progress and make a broadly protective vaccine feasible.

摘要

产肠毒素大肠杆菌(ETEC)是一种多样且基因可塑性强的病理变种(致病型),其定义依据是能产生不耐热肠毒素(LT)和耐热肠毒素(ST)。这些病原体在四十多年前因致使患者出现严重霍乱样腹泻而被发现,如今已知每年会引发数亿例有症状感染。世界中低收入地区缺乏清洁水源和基本卫生设施的儿童受ETEC影响尤为严重。除了导致急性腹泻发病外,这些病原体仍是五岁以下儿童死亡的重要原因,还多次与儿童营养不良和生长发育迟缓的后遗症相关联。因此,能够预防ETEC感染的疫苗仍然是重中之重。尽管经过了几十年的努力,研发出一种能预防这些病原体广泛感染的许可疫苗仍是一个理想目标,而且ETEC潜在的基因可塑性对开发涵盖其完整抗原谱的疫苗构成了根本挑战。然而,包括类毒素在内的新策略、对ETEC分子发病机制更全面的理解、目标免疫原的结构细节以及发现对毒力至关重要的更高度保守抗原,应能加速进展并使一种具有广泛保护作用的疫苗成为可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/156d/9355458/461f38679187/nihms-1769336-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/156d/9355458/461f38679187/nihms-1769336-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/156d/9355458/461f38679187/nihms-1769336-f0001.jpg

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