Neisseria Research Group, Molecular Microbiology, Academic School of Clinical and Experimental Sciences, University of Southampton Faculty of Medicine, Southampton, United Kingdom.
Front Cell Infect Microbiol. 2022 Mar 22;12:861489. doi: 10.3389/fcimb.2022.861489. eCollection 2022.
pathogens express a Macrophage Infectivity Potentiator Protein (MIP), which belongs to the FK506 binding protein (FKBP) family of proteins that exhibit peptidyl-prolyl cis/trans isomerase (PPIase) activity. MIP proteins are potential candidates for inclusion into vaccines for gonorrhoea caused by infection, and meningitis/sepsis caused by infection. MIP proteins are also potential targets for directed drug treatments, although this remains relatively unexplored. In this mini-review, we provide an update into the vaccine potential of MIP and the few published drug targeting studies, and explore further the diversity of this protein amongst both pathogenic and commensal spp.
病原体表达巨噬细胞感染增强蛋白(MIP),该蛋白属于 FK506 结合蛋白(FKBP)家族,具有肽脯氨酰顺/反式异构酶(PPIase)活性。MIP 蛋白是淋病(由 感染引起)和脑膜炎/败血症(由 感染引起)疫苗的潜在候选物。MIP 蛋白也是靶向药物治疗的潜在靶点,尽管这方面的研究相对较少。在这篇综述中,我们提供了关于 MIP 的疫苗潜力和少数已发表的药物靶向研究的最新信息,并进一步探讨了这种蛋白在致病性和共生 spp 中的多样性。