Bioprocess Scale Up Facility, Defence Research and Development Establishment, Gwalior, India.
Division of Virology, Defence Research and Development Establishment, Gwalior, India.
Front Immunol. 2018 Aug 23;9:1919. doi: 10.3389/fimmu.2018.01919. eCollection 2018.
Recombinant proteins are gaining enormous importance these days due to their wide application as biopharmaceutical products and proven safety record. Various recombinant proteins of therapeutic and prophylactic importance have been successfully produced in microbial and higher expression host systems. Since there is no specific antiviral therapy available against dengue, the prevention by vaccination is the mainstay in reducing the disease burden. Therefore, efficacious vaccines are needed to control the spread of dengue worldwide. Dengue is an emerging viral disease caused by any of dengue virus 1-4 serotypes that affects the human population around the globe. Dengue virus is a single stranded RNA virus encoding three structural proteins (capsid protein, pre-membrane protein, and envelope protein) and seven non-structural proteins (NS1, NS2a, NS2b, NS3, NS4a, NS4b, NS5). As the only licensed dengue vaccine (Dengvaxia) is unable to confer balanced protection against all the serotypes, therefore various approaches for development of dengue vaccines including tetravalent live attenuated, inactivated, plasmid DNA, virus-vectored, virus-like particles, and recombinant subunit vaccines are being explored. These candidates are at different stages of vaccine development and have their own merits and demerits. The promising subunit vaccines are mainly based on envelope or its domain and non-structural proteins of dengue virus. These proteins have been produced in different hosts and are being investigated for development of a successful dengue vaccine. Novel immunogens have been designed employing various strategies like protein engineering and fusion of antigen with various immunostimulatory motif to work as self-adjuvant. Moreover, recombinant proteins can be formulated with novel adjuvants to enhance the immunogenicity and thus conferring better protection to the vaccinees. With the advent of newer and safer host systems, these recombinant proteins can be produced in a cost effective manner at large scale for vaccine studies. In this review, we summarize recent developments in recombinant protein based dengue vaccines that could lead to a good number of efficacious vaccine candidates for future human use and ultimately alternative dengue vaccine candidates.
由于其在生物制药产品中的广泛应用和经过验证的安全性记录,重组蛋白在当今变得越来越重要。已经在微生物和高表达宿主系统中成功生产出各种具有治疗和预防重要性的重组蛋白。由于目前尚无针对登革热的特异性抗病毒疗法,因此疫苗接种预防是减轻疾病负担的主要手段。因此,需要有效的疫苗来控制登革热在全球的传播。登革热是一种由登革病毒 1-4 型血清型引起的新兴病毒性疾病,影响着全球的人类人口。登革热病毒是一种单链 RNA 病毒,编码三种结构蛋白(衣壳蛋白、前膜蛋白和包膜蛋白)和七种非结构蛋白(NS1、NS2a、NS2b、NS3、NS4a、NS4b、NS5)。由于唯一获得许可的登革热疫苗(Dengvaxia)无法对所有血清型提供均衡的保护,因此正在探索开发登革热疫苗的各种方法,包括四价减毒活疫苗、灭活疫苗、质粒 DNA、病毒载体疫苗、病毒样颗粒疫苗和重组亚单位疫苗。这些候选疫苗处于疫苗开发的不同阶段,各有优缺点。有前途的亚单位疫苗主要基于登革热病毒的包膜或其结构域和非结构蛋白。这些蛋白已在不同的宿主中产生,并正在研究用于开发成功的登革热疫苗。新型免疫原已通过各种策略设计,如蛋白质工程和将抗原与各种免疫刺激性基序融合,以作为自佐剂发挥作用。此外,重组蛋白可以与新型佐剂联合使用,以提高免疫原性,从而为疫苗接种者提供更好的保护。随着更新、更安全的宿主系统的出现,这些重组蛋白可以以具有成本效益的方式大规模生产,用于疫苗研究。在这篇综述中,我们总结了基于重组蛋白的登革热疫苗的最新进展,这些进展可能会为未来人类使用带来大量有效的候选疫苗,并最终替代登革热候选疫苗。