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猴腺病毒作为疫苗载体。

Simian adenoviruses as vaccine vectors.

作者信息

Morris Susan J, Sebastian Sarah, Spencer Alexandra J, Gilbert Sarah C

机构信息

Jenner Institute, ORCRB, University of Oxford, Off Roosevelt Drive, Headington, Oxford, OX3 7DQ, UK.

出版信息

Future Virol. 2016 Sep;11(9):649-659. doi: 10.2217/fvl-2016-0070. Epub 2016 Sep 15.

Abstract

Replication incompetent human adenovirus serotype 5 (HAdV-C5) has been extensively used as a delivery vehicle for gene therapy proteins and infectious disease antigens. These vectors infect replicating and nonreplicating cells, have a broad tissue tropism, elicit high immune responses and are easily purified to high titers. However, the utility of HAdV-C5 vectors as potential vaccines is limited due to pre-existing immunity within the human population that significantly reduces the immunogenicity of HAdV-C5 vaccines. In recent years, adenovirus vaccine development has focused on simian-derived adenoviral vectors, which have the desirable vector characteristics of HAdV-C5 but with negligible seroprevalence in the human population. Here, we discuss recent advances in simian adenovirus vaccine vector development and evaluate current research specifically focusing on clinical trial data.

摘要

复制缺陷型人5型腺病毒(HAdV-C5)已被广泛用作基因治疗蛋白和传染病抗原的递送载体。这些载体可感染正在复制和非复制的细胞,具有广泛的组织嗜性,引发强烈的免疫反应,并且易于纯化至高滴度。然而,由于人群中预先存在的免疫力会显著降低HAdV-C5疫苗的免疫原性,HAdV-C5载体作为潜在疫苗的效用受到限制。近年来,腺病毒疫苗的开发主要集中在猿猴来源的腺病毒载体上,这些载体具有HAdV-C5理想的载体特性,但在人群中的血清阳性率可忽略不计。在此,我们讨论猿猴腺病毒疫苗载体开发的最新进展,并特别针对临床试验数据评估当前的研究情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52ff/5842362/058e2e1f76ae/fvl-11-649-g1.jpg

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