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基于表达致死毒素成分突变变体的菌株的高效、无毒炭疽芽孢杆菌疫苗。

Efficacious, nontoxigenic Bacillus anthracis spore vaccines based on strains expressing mutant variants of lethal toxin components.

作者信息

Mendelson I, Gat O, Aloni-Grinstein R, Altboum Z, Inbar I, Kronman C, Bar-Haim E, Cohen S, Velan B, Shafferman A

机构信息

Department of Biochemistry and Molecular Genetics, Israel Institute for Biological Research, P.O. Box 19, Ness-Ziona 74100, Israel.

出版信息

Vaccine. 2005 Dec 1;23(48-49):5688-97. doi: 10.1016/j.vaccine.2004.11.077. Epub 2005 Feb 5.

Abstract

We reported previously on the development of a Bacillus anthracis vaccine strain expressing high levels of recombinant protective antigen (rPA) [Cohen et al., Infec Immun 2000;68(8):4549-58]. To further explore the potential of the B. anthracis platform, we generated several attenuated strains expressing lethal toxin components PA and LF, which are biologically inactive, yet retain their antigenic properties. A single injection of 5 x 10(7) spores of one of these strains, carrying PA mutation at a site involved in effector translocation (residues 313-314) was shown to resemble wild type PA in inducing production of high levels of anti-PA neutralizing antibodies and producing effective protective immunity for 12 months. Long-term protection and persistence of functional antibody titers was observed after the gradual elimination of spores from guinea pig tissues 3 months after injection and in the measurable absence of bacteria in tissues. The mutant toxin components could, thus be an effective alternatives to their native counterparts when presented to the immune system in context of a live B. anthracis strain. These live vaccine prototypes may serve as a platform for future multi-component vaccines.

摘要

我们之前报道过一种表达高水平重组保护性抗原(rPA)的炭疽芽孢杆菌疫苗株的研发情况[科恩等人,《感染与免疫》2000年;68(8):4549 - 58]。为了进一步探索炭疽芽孢杆菌平台的潜力,我们构建了几种表达致死毒素成分PA和LF的减毒株,这些成分虽无生物学活性,但保留了其抗原特性。单次注射5×10⁷个其中一种菌株的孢子,该菌株在参与效应物转运的位点(第313 - 314位氨基酸)携带PA突变,结果显示在诱导产生高水平抗PA中和抗体以及产生长达12个月的有效保护性免疫方面类似于野生型PA。在注射后3个月豚鼠组织中的孢子逐渐清除且组织中可检测到无细菌存在后,观察到了长期保护以及功能性抗体滴度的持续存在。因此,当在活炭疽芽孢杆菌菌株的背景下呈现给免疫系统时,突变毒素成分可能是其天然对应物的有效替代物。这些活疫苗原型可作为未来多组分疫苗的一个平台。

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