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外膜蛋白 C 是对抗福氏 3a 志贺菌的保护性和独特的疫苗抗原。

Outer membrane protein C is a protective and unique vaccine antigen against Shigella flexneri 3a.

机构信息

Hirszfeld Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Weigla Str. 12, 53-114, Wroclaw, Poland.

Department of Animal Products Technology and Quality Management, Wroclaw University of Environmental and Life Sciences, Chelmonskiego Str. 37/41, 51-630, Wroclaw, Poland.

出版信息

Sci Rep. 2024 Oct 25;14(1):25398. doi: 10.1038/s41598-024-76745-8.

Abstract

The anti-Shigella vaccine is one of the WHO's top priorities. Every year the disease kills more than 200,000 people worldwide and poses a serious threat to children under 5 years of age and the elderly. Increasing antibiotic resistance and limitations in diagnostics emphasize the need to develop an effective vaccine. Recent research and clinical trials report multiple approaches used in Shigella-vaccine development. However, despite the efforts of researchers, pharmaceutical companies and health care organizations, there is no licensed vaccine against shigellosis available to the community. Here, we expressed, broadly characterized and demonstrated the protective properties of outer membrane protein C as an effective molecule serving as a universal antigen for Shigella vaccine. Most of the current approaches to the development of Shigella vaccine are based on the polysaccharide antigens, which are serotype specific and have always been challenging in terms of their high specificity, targeting the most exposed surface antigens identified for certain Shigella serotypes. Here, we confirm immunogenic and protective properties of the recombinant OmpC protein, which protects mice against a lethal dose of a virulent strain 2 weeks after active immunization.

摘要

抗志贺氏菌疫苗是世界卫生组织的重点项目之一。每年,该疾病在全球导致超过 20 万人死亡,对 5 岁以下儿童和老年人构成严重威胁。抗生素耐药性的增加和诊断方法的局限性强调了开发有效疫苗的必要性。最近的研究和临床试验报告了多种用于志贺氏菌疫苗开发的方法。然而,尽管研究人员、制药公司和医疗机构做出了努力,但社区仍没有获得针对志贺氏菌病的许可疫苗。在这里,我们表达、广泛表征并证明了外膜蛋白 C 作为一种有效的通用抗原在志贺氏菌疫苗中的保护特性。目前大多数开发志贺氏菌疫苗的方法都是基于多糖抗原,这些抗原具有血清型特异性,而且由于其高度特异性,一直以来都是一个挑战,因为它们针对的是某些志贺氏菌血清型最暴露的表面抗原。在这里,我们证实了重组 OmpC 蛋白的免疫原性和保护特性,该蛋白在主动免疫 2 周后可保护小鼠免受致死剂量的强毒菌株的侵害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/10bd/11511853/4d0d3f0269ae/41598_2024_76745_Fig1_HTML.jpg

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