Liu Jinliang, Dai Shiyu, Wang Manli, Hu Zhihong, Wang Hualin, Deng Fei
State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.
Virol Sin. 2016 Aug;31(4):279-87. doi: 10.1007/s12250-016-3756-y. Epub 2016 Jul 11.
Emerging infectious diseases are major threats to human health. Most severe viral disease outbreaks occur in developing regions where health conditions are poor. With increased international travel and business, the possibility of eventually transmitting infectious viruses between different countries is increasing. The most effective approach in preventing viral diseases is vaccination. However, vaccines are not currently available for numerous viral diseases. Virus-like particles (VLPs) are engineered vaccine candidates that have been studied for decades. VLPs are constructed by viral protein expression in various expression systems that promote the selfassembly of proteins into structures resembling virus particles. VLPs have antigenicity similar to that of the native virus, but are non-infectious as they lack key viral genetic material. VLP vaccines have attracted considerable research interest because they offer several advantages over traditional vaccines. Studies have shown that VLP vaccines can stimulate both humoral and cellular immune responses, which may offer effective antiviral protection. Here we review recent developments with VLP-based vaccines for several highly virulent emerging or re-emerging infectious diseases. The infectious agents discussed include RNA viruses from different virus families, such as the Arenaviridae, Bunyaviridae, Caliciviridae, Coronaviridae, Filoviridae, Flaviviridae, Orthomyxoviridae, Paramyxoviridae, and Togaviridae families.
新发传染病是对人类健康的重大威胁。大多数严重的病毒性疾病暴发发生在卫生条件较差的发展中地区。随着国际旅行和商业活动的增加,最终在不同国家之间传播传染性病毒的可能性也在增加。预防病毒性疾病最有效的方法是接种疫苗。然而,目前许多病毒性疾病尚无可用疫苗。病毒样颗粒(VLP)是经过几十年研究的工程疫苗候选物。VLP是通过在各种表达系统中表达病毒蛋白构建而成的,这些表达系统能促进蛋白质自组装成类似病毒颗粒的结构。VLP具有与天然病毒相似的抗原性,但由于缺乏关键的病毒遗传物质而无传染性。VLP疫苗因其比传统疫苗具有多种优势而引起了相当大的研究兴趣。研究表明,VLP疫苗可刺激体液免疫和细胞免疫反应,这可能提供有效的抗病毒保护。在此,我们综述了基于VLP的疫苗针对几种高致病性新发或再发传染病的最新进展。所讨论的传染源包括来自不同病毒科的RNA病毒,如沙粒病毒科、布尼亚病毒科、杯状病毒科、冠状病毒科、丝状病毒科、黄病毒科、正粘病毒科、副粘病毒科和披膜病毒科。