一种有前途的金黄色葡萄球菌疫苗佐剂候选物,基于先天免疫克服葡萄球菌感染。

IF 1.3 Q4 IMMUNOLOGY
Clinical and Experimental Vaccine Research Pub Date : 2025-07-01 Epub Date: 2025-06-13 DOI:10.7774/cevr.2025.14.e27
Xinrui Mao, Thomas Söderhäll, Gi-Sub Choi, Jin-Han Kang, Cunwei Cao, Qinghua Yuan
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引用次数: 0

摘要

金黄色葡萄球菌介导的人类疾病范围从轻微的皮肤感染到危及生命的疾病。在过去,由这种细菌引起的感染可以用抗生素治疗。然而,这个物种对抗生素的耐药性越来越强。因此,迫切需要疫苗作为替代治疗工具来控制这一麻烦的病原体。但到目前为止,所有用于预防金黄色葡萄球菌感染的人体临床试验疫苗都失败了。这种失败的主要原因可以总结为:1)有效抗原尚未确定;2)宿主对金黄色葡萄球菌的保护性免疫反应尚不清楚;3)尚未找到良好的动物模型。最关键的挑战是,尽管血清免疫球蛋白G滴度很高,但接种疫苗的宿主无法消除细胞内的金黄色葡萄球菌。为了解决这一问题,必须设计和开发一种同时诱导体液免疫和细胞免疫的疫苗。根据我们的研究经验和最近其他小组发表的数据,我们提出微生物糖共聚物可以激活宿主先天免疫,可以考虑作为一种新的金黄色葡萄球菌疫苗佐剂。在此,我们的综述旨在强调碳水化合物免疫生物学的最新进展如何指导设计和开发更好的金黄色葡萄球菌疫苗和佐剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A promising <i>Staphylococcus aureus</i> vaccine adjuvant candidate to overcome <i>Staphylococcal</i> infection based on innate immunity.

A promising <i>Staphylococcus aureus</i> vaccine adjuvant candidate to overcome <i>Staphylococcal</i> infection based on innate immunity.

A promising <i>Staphylococcus aureus</i> vaccine adjuvant candidate to overcome <i>Staphylococcal</i> infection based on innate immunity.

A promising Staphylococcus aureus vaccine adjuvant candidate to overcome Staphylococcal infection based on innate immunity.

Staphylococcus aureus-mediated human disease ranges from minor skin infection to life threatening diseases. In the past, infections caused by this bacterium could be treated with antibiotics. However, this species has become increasingly resistant to antibiotics. Therefore, vaccines as alternative therapeutic tools is urgently required for controlling this troubles pathogen. But thus far, all vaccines in human clinical trials for preventing S. aureus infections have failed. Three major reasons for this failure can be summarized: 1) An effective antigen has not yet been identified; 2) Host protective immune responses against S. aureus are unclear; 3) Good animal model is not yet identified. The most critical challenge is that despite robust serum immunoglobulin G titers, vaccinated hosts fail to eliminate intracellular S. aureus. To solve this problem, a vaccine inducing both humoral- and cellular-immunity should be designed and developed. Based on our research experiences and recent other groups' published data, we propose that microbial glycopolymers, which are activating host innate immunity, should be considered as a new S. aureus vaccine adjuvant. Here, our review aims at highlighting how the latest advances in carbohydrates immunobiology can guide the design and development of better S. aureus vaccines and adjuvants.

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来源期刊
CiteScore
3.70
自引率
3.70%
发文量
29
审稿时长
8 weeks
期刊介绍: Clin Exp Vaccine Res, the official English journal of the Korean Vaccine Society, is an international, peer reviewed, and open-access journal. It covers all areas related to vaccines and vaccination. Clin Exp Vaccine Res publishes editorials, review articles, special articles, original articles, case reports, brief communications, and correspondences covering a wide range of clinical and experimental subjects including vaccines and vaccination for human and animals against infectious diseases caused by viruses, bacteria, parasites and tumor. The scope of the journal is to disseminate information that may contribute to elaborate vaccine development and vaccination strategies targeting infectious diseases and tumors in human and animals. Relevant topics range from experimental approaches to (pre)clinical trials for the vaccine research based on, but not limited to, basic laboratory, translational, and (pre)clinical investigations, epidemiology of infectious diseases and progression of all aspects in the health related issues. It is published printed and open accessed online issues (https://ecevr.org) two times per year in 31 January and 31 July. Clin Exp Vaccine Res is linked to many international databases and is made freely available to institutions and individuals worldwide
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