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A 组链球菌 covR/S 突变株的细胞相互作用。

Cellular interactions of covR/S mutant group A Streptococci.

机构信息

Institute for Glycomics, Griffith University, Gold Coast, Queensland, 4222, Australia.

Institute for Glycomics, Griffith University, Gold Coast, Queensland, 4222, Australia.

出版信息

Microbes Infect. 2018 Oct-Nov;20(9-10):531-535. doi: 10.1016/j.micinf.2017.12.009. Epub 2017 Dec 26.

Abstract

Group A Streptococci (GAS) are responsible for a wide array of non-invasive and invasive diseases and varying immune sequelae with high rates of mortality and morbidity. GAS strains with a mutation in their covR/S regulatory system are hypervirulent with an increased capacity for causing invasive disease. covR/S mutants augment their virulence through the up-regulation of important virulence factors and target host immune surveillance primarily by inhibiting neutrophils. An in-depth understanding of the immunopathogenesis of covR/S mutants will facilitate the development of vaccine strategies and design. Ultimately, by targeting separate virulence mechanisms, multi-component vaccines may provide improved protective efficacy against hypervirulent GAS infections.

摘要

A 群链球菌(GAS)可引起广泛的非侵袭性和侵袭性疾病,并产生不同的免疫后遗症,具有较高的死亡率和发病率。其 covR/S 调节系统发生突变的 GAS 菌株具有超强毒力,侵袭性疾病的发生率更高。covR/S 突变株通过上调重要的毒力因子并主要通过抑制中性粒细胞来逃避宿主的免疫监视,从而增强其毒力。深入了解 covR/S 突变株的免疫发病机制将有助于疫苗策略和设计的制定。最终,通过针对不同的毒力机制,多组分疫苗可能提供针对超强毒力 GAS 感染的更好的保护效力。

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