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Immunogenicity and Vaccine Potential of InsB an ESAT-6-Like Antigen Identified in the Highly Virulent Mycobacterium tuberculosis Beijing K Strain

机译:InsB的免疫原性和疫苗潜力在高毒力结核分枝杆菌北京K株中鉴定出类似于ESAT-6的抗原。

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摘要

Our group recently identified InsB, an ESAT-6-like antigen belonging to the Mtb9.9 subfamily within the Esx family, in the Mycobacterium tuberculosis Korean Beijing strain (Mtb K) via a comparative genomic analysis with that of the reference Mtb H37Rv and characterized its immunogenicity and its induced immune response in patients with tuberculosis (TB). However, the vaccine potential of InsB has not been fully elucidated. In the present study, InsB was evaluated as a subunit vaccine in comparison with the most well-known ESAT-6 against the hypervirulent Mtb K. Mice immunized with InsB/MPL-DDA exhibited an antigen-specific IFN-γ response along with antigen-specific effector/memory T cell expansion in the lungs and spleen upon antigen restimulation. In addition, InsB immunization markedly induced multifunctional Th1-type CD4+ T cells coexpressing TNF-α, IL-2, and IFN-γ in the lungs following Mtb K challenge. Finally, we found that InsB immunization conferred long-term protection against Mtb K comparable to that conferred by ESAT-6 immunization, as evidenced by a similar level of CFU reduction in the lung and spleen and reduced lung inflammation. These results suggest that InsB may be an excellent vaccine antigen component for developing a multiantigenic Mtb subunit vaccine by generating Th1-biased memory T cells with a multifunctional capacity and may confer durable protection against the highly virulent Mtb K.
机译:我们的小组最近通过与参考Mtb H37Rv进行的比较基因组分析,在结核分枝杆菌北京北京菌株(Mtb K)中鉴定了InsB(一种属于Esx家族Mtb9.9亚家族的ESAT-6样抗原),并进行了特征分析结核病患者的免疫原性及其诱导的免疫反应。但是,尚未完全阐明InsB的疫苗潜力。在本研究中,与最著名的针对高毒Mtb K的ESAT-6相比,InsB被评估为亚单位疫苗。用InsB / MPL-DDA免疫的小鼠表现出抗原特异性IFN-γ反应以及抗原-抗原再刺激后,肺和脾脏中的特异性效应子/记忆T细胞扩增。此外,InsB免疫显着诱导Mtb K攻击后肺中共表达TNF-α,IL-2和IFN-γ的多功能Th1型CD4 + T细胞。最后,我们发现InsB免疫可长期抵抗Mtb K,与ESAT-6免疫相比具有长期保护作用,肺和脾脏CFU减少水平相似,肺部炎症减少程度也证明了这一点。这些结果表明,InsB可能是通过产生具有多功能功能的Th1偏向性记忆T细胞而开发多抗原Mtb亚单位疫苗的优良疫苗抗原成分,并且可以针对高毒性Mtb K给予持久保护。

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