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黑猩猩腺病毒疫苗可预防扎伊尔埃博拉病毒。

Chimpanzee adenovirus vaccine protects against Zaire Ebola virus.

作者信息

Kobinger Gary P, Feldmann Heinz, Zhi Yan, Schumer Gregory, Gao Guangping, Feldmann Friederike, Jones Steven, Wilson James M

机构信息

Special Pathogens Program, National Microbiology Laboratory, Health Canada, Canadian Science Centre for Human and Animal Health, University of Manitoba, Winnipeg, Canada.

出版信息

Virology. 2006 Mar 15;346(2):394-401. doi: 10.1016/j.virol.2005.10.042. Epub 2005 Dec 13.

Abstract

This study evaluated the use of a chimpanzee-based adenovirus vaccine in mouse and Guinea pigs models of Zaire Ebola virus (ZEBOV) infection. Vaccine vector expressing the envelope glycoprotein of ZEBOV was created from the molecular clone of chimpanzee adenovirus pan7 (AdC7). AdC7 vaccine stimulated robust T and B cell responses to ZEBOV in naïve mice inducing complete protection to an otherwise lethal challenge of ZEBOV. Complete protection to Zaire Ebola virus was also observed in Guinea pigs vaccinated with a relatively low dose of AdC7 (5 x 10(9)/kg). Pre-existing immunity to AdHu5 was generated in mice following pre-exposure to AdHu5 or administration of pooled human immune globulin. Pre-existing immunity to human adenoviruses severely compromised the efficacy of the human AdHu5 vaccine but not the chimpanzee AdC7 vaccine. These results validate further development of Chimpanzee-based vaccine and highlight the impact of pre-existing immunity to the vaccine carrier.

摘要

本研究评估了一种基于黑猩猩腺病毒的疫苗在扎伊尔埃博拉病毒(ZEBOV)感染的小鼠和豚鼠模型中的应用。表达ZEBOV包膜糖蛋白的疫苗载体由黑猩猩腺病毒pan7(AdC7)的分子克隆构建而成。AdC7疫苗在未接触过抗原的小鼠中激发了针对ZEBOV的强大T细胞和B细胞反应,对ZEBOV的致死性攻击产生了完全保护作用。在用相对低剂量的AdC7(5×10⁹/kg)接种的豚鼠中也观察到了对扎伊尔埃博拉病毒的完全保护。在小鼠预先接触AdHu5或给予人免疫球蛋白混合液后,产生了对AdHu5的预先免疫。对人腺病毒的预先免疫严重损害了人AdHu5疫苗的效力,但未影响黑猩猩AdC7疫苗的效力。这些结果证实了基于黑猩猩的疫苗的进一步研发,并突出了预先免疫对疫苗载体的影响。

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