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在小鼠中,一种 chimpanzee 腺病毒载体的裂谷热疫苗的免疫原性和功效。

Immunogenicity and efficacy of a chimpanzee adenovirus-vectored Rift Valley fever vaccine in mice.

机构信息

The Jenner Institute, University of Oxford, Oxford, UK.

出版信息

Virol J. 2013 Dec 5;10:349. doi: 10.1186/1743-422X-10-349.

Abstract

BACKGROUND

Rift Valley Fever (RVF) is a viral zoonosis that historically affects livestock production and human health in sub-Saharan Africa, though epizootics have also occurred in the Arabian Peninsula. Whilst an effective live-attenuated vaccine is available for livestock, there is currently no licensed human RVF vaccine. Replication-deficient chimpanzee adenovirus (ChAd) vectors are an ideal platform for development of a human RVF vaccine, given the low prevalence of neutralizing antibodies against them in the human population, and their excellent safety and immunogenicity profile in human clinical trials of vaccines against a wide range of pathogens.

METHODS

Here, in BALB/c mice, we evaluated the immunogenicity and efficacy of a replication-deficient chimpanzee adenovirus vector, ChAdOx1, encoding the RVF virus envelope glycoproteins, Gn and Gc, which are targets of virus neutralizing antibodies. The ChAdOx1-GnGc vaccine was assessed in comparison to a replication-deficient human adenovirus type 5 vector encoding Gn and Gc (HAdV5-GnGc), a strategy previously shown to confer protective immunity against RVF in mice.

RESULTS

A single immunization with either of the vaccines conferred protection against RVF virus challenge eight weeks post-immunization. Both vaccines elicited RVF virus neutralizing antibody and a robust CD8+ T cell response.

CONCLUSIONS

Together the results support further development of RVF vaccines based on replication-deficient adenovirus vectors, with ChAdOx1-GnGc being a potential candidate for use in future human clinical trials.

摘要

背景

裂谷热(RVF)是一种病毒性人畜共患病,历史上影响撒哈拉以南非洲的牲畜生产和人类健康,但在阿拉伯半岛也曾发生过动物疫病。虽然有针对牲畜的有效减毒活疫苗,但目前尚无许可的人类 RVF 疫苗。复制缺陷型黑猩猩腺病毒(ChAd)载体是开发人类 RVF 疫苗的理想平台,因为人类对它们的中和抗体的流行率低,并且在针对广泛病原体的疫苗的人类临床试验中,它们具有出色的安全性和免疫原性。

方法

在这里,我们在 BALB/c 小鼠中评估了编码 RVF 病毒包膜糖蛋白 Gn 和 Gc 的复制缺陷型黑猩猩腺病毒载体 ChAdOx1 的免疫原性和疗效,Gn 和 Gc 是病毒中和抗体的靶标。与编码 Gn 和 Gc 的复制缺陷型人 5 型腺病毒载体(HAdV5-GnGc)相比,评估了 ChAdOx1-GnGc 疫苗,该策略先前已证明可在小鼠中提供针对 RVF 的保护免疫力。

结果

单次免疫这两种疫苗均可在免疫后 8 周内预防 RVF 病毒攻击。两种疫苗都能引起 RVF 病毒中和抗体和强大的 CD8+ T 细胞反应。

结论

这些结果共同支持进一步开发基于复制缺陷型腺病毒载体的 RVF 疫苗,ChAdOx1-GnGc 是未来人类临床试验中使用的潜在候选疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c1c/4235025/c804466e515a/1743-422X-10-349-1.jpg

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