Lee Tae Hee, Chung Kyung Min
Department of Microbiology and Immunology.
Institute for Medical Science, Chonbuk National University Medical School, Jeonju, Jeonbuk, 561-756, Korea.
Microbiol Immunol. 2015 Sep;59(9):555-61. doi: 10.1111/1348-0421.12284.
Recent studies have defined several virulence factors as vaccine candidates against Vibrio vulnificus. However, most of these factors have the potential to cause pathogenic effects in the vaccinees or induce incomplete protection. To overcome these drawbacks, a catalytically inactive form, CPDVv (C3725S), of the well-conserved cysteine protease domain (CPD) of V. vulnificus multifunctional autoprocessing repeats-in-toxin (MARTXVv /RtxA1) was recombinantly generated and characterized. Notably, active and passive immunization with CPDVv (C3725S) conferred protective immunity against V. vulnificus strains. These results may provide a novel framework for developing safe and efficient subunit vaccines and/or therapeutics against V. vulnificus that target the CPD of MARTX toxins.
最近的研究已将几种毒力因子定义为针对创伤弧菌的候选疫苗。然而,这些因子中的大多数有可能在疫苗接种者中引起致病作用或诱导不完全保护。为克服这些缺点,创伤弧菌多功能自加工重复毒素(MARTXVv /RtxA1)中保守的半胱氨酸蛋白酶结构域(CPD)的催化失活形式CPDVv(C3725S)被重组生成并进行了表征。值得注意的是,用CPDVv(C3725S)进行主动和被动免疫可赋予针对创伤弧菌菌株的保护性免疫。这些结果可能为开发针对创伤弧菌的安全有效的亚单位疫苗和/或疗法提供一个新的框架,该疫苗和/或疗法靶向MARTX毒素的CPD。