Lacey Keenan A, Geoghegan Joan A, McLoughlin Rachel M
Host Pathogen Interactions Group, School of Biochemistry and Immunology, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.
Microbiology Department, Moyne Institute of Preventive Medicine, Trinity College Dublin, Dublin 2, Ireland.
Pathogens. 2016 Feb 17;5(1):22. doi: 10.3390/pathogens5010022.
Staphylococcus aureus (S. aureus) causes the vast majority of skin and soft tissue infections (SSTIs) in humans. S. aureus has become increasingly resistant to antibiotics and there is an urgent need for new strategies to tackle S. aureus infections. Vaccines offer a potential solution to this epidemic of antimicrobial resistance. However, the development of next generation efficacious anti-S. aureus vaccines necessitates a greater understanding of the protective immune response against S. aureus infection. In particular, it will be important to ascertain if distinct immune mechanisms are required to confer protection at distinct anatomical sites. Recent discoveries have highlighted that interleukin-17-producing T cells play a particularly important role in the immune response to S. aureus skin infection and suggest that vaccine strategies to specifically target these types of T cells may be beneficial in the treatment of S. aureus SSTIs. S. aureus expresses a large number of cell wall-anchored (CWA) proteins, which are covalently attached to the cell wall peptidoglycan. The virulence potential of many CWA proteins has been demonstrated in infection models; however, there is a paucity of information regarding their roles during SSTIs. In this review, we highlight potential candidate antigens for vaccines targeted at protection against SSTIs.
金黄色葡萄球菌(S. aureus)引发了人类绝大多数的皮肤和软组织感染(SSTIs)。金黄色葡萄球菌对抗生素的耐药性日益增强,因此迫切需要新的策略来应对金黄色葡萄球菌感染。疫苗为解决这种抗菌药物耐药性流行问题提供了一种潜在的解决方案。然而,开发下一代有效的抗金黄色葡萄球菌疫苗需要更深入地了解针对金黄色葡萄球菌感染的保护性免疫反应。特别是,确定在不同解剖部位提供保护是否需要不同的免疫机制将非常重要。最近的发现强调,产生白细胞介素-17的T细胞在对金黄色葡萄球菌皮肤感染的免疫反应中发挥着特别重要的作用,并表明专门针对这些类型T细胞的疫苗策略可能对治疗金黄色葡萄球菌SSTIs有益。金黄色葡萄球菌表达大量细胞壁锚定(CWA)蛋白,这些蛋白共价连接到细胞壁肽聚糖上。许多CWA蛋白的毒力潜力已在感染模型中得到证实;然而,关于它们在SSTIs期间的作用的信息却很少。在这篇综述中,我们重点介绍了针对预防SSTIs的疫苗的潜在候选抗原。