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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Structural features of HtpG(Mtb) and HtpG-ESAT6(Mtb) vaccine antigens against tuberculosis: Molecular determinants of antigenic synergy and cytotoxicity modulation
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Structural features of HtpG(Mtb) and HtpG-ESAT6(Mtb) vaccine antigens against tuberculosis: Molecular determinants of antigenic synergy and cytotoxicity modulation

机译:HTPG(MTB)和HTPG-ESAT6(MTB)疫苗抗原对结核病的结构特征:抗原协同作用和细胞毒性调节的分子决定因素

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摘要

Vaccine development against tuberculosis is an urgent need as the only available vaccine, M. bovis Bacillus Calmette Guerin (BCG), is unable to provide significant protection in adults. Among newly identified antigens, Rv2299c is an excellent candidate for the rational design of an effective multi-antigenic TB vaccine. Also, when fused to the T cell antigen ESAT6, it becomes highly effective in boosting BCG immunization and it adopts low cytotoxicity compared to ESAT6.
机译:对肺结核的疫苗开发是一种迫切需要作为唯一可用的疫苗,M.Bovis Bacillus Calmette Guerin(BCG),无法在成年人中提供显着的保护。 在新鉴定的抗原中,RV2299C是有效多抗原TB疫苗的理性设计的优异候选者。 此外,当与T细胞抗原ESAT6融合时,它在增强BCG免疫方面变得非常有效,并且与ESAT6相比,它采用低细胞毒性。

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