Discovery of B-cell epitopes for development of dengue vaccines and antibody therapeutics.

IF 3 3区 医学 Q1 IMMUNOLOGY Medical Microbiology and Immunology Pub Date : 2022-02-01 Epub Date: 2022-01-21 DOI:10.1007/s00430-021-00726-1
Mohd Ishtiaq Anasir, Chit Laa Poh
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引用次数: 2

Abstract

Dengue is one of the most frequently transmitted viral infections globally which creates a serious burden to the healthcare system in many countries in the tropical and subtropical regions. To date, no vaccine has demonstrated balanced protection against the four dengue serotypes. Dengvaxia as the only vaccine that has been licensed for use in endemic areas has shown an increased risk in dengue-naïve vaccines to develop severe dengue. A crucial element in protection from dengue infection is the neutralizing antibody responses. Therefore, the identification of protective linear B-cell epitopes can guide vaccine design and facilitate the development of monoclonal antibodies as dengue therapeutics. This review summarizes the identification of dengue B-cell epitopes within the envelope (E) protein of dengue that can be incorporated into peptide vaccine constructs. These epitopes have been identified through approaches such as bioinformatics, three-dimensional structure analysis of antibody-dengue complexes, mutagenesis/alanine scanning and escape mutant studies. Additionally, the therapeutic potential of monoclonal antibodies targeting the E protein of dengue is reviewed. This can provide a basis for the design of future dengue therapies.

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b细胞表位的发现有助于登革热疫苗和抗体疗法的开发。
登革热是全球传播最频繁的病毒感染之一,对热带和亚热带地区许多国家的卫生保健系统造成严重负担。迄今为止,还没有疫苗显示出对四种登革热血清型具有均衡的保护作用。作为唯一获准在流行地区使用的登卡夏疫苗,dengue-naïve疫苗显示出发展为严重登革热的风险增加。预防登革热感染的一个关键因素是中和抗体反应。因此,确定具有保护作用的线性b细胞表位可以指导疫苗设计,并促进单克隆抗体作为登革热治疗药物的开发。本文综述了登革热包膜(E)蛋白内可被纳入肽疫苗构建体的登革热b细胞表位的鉴定。这些表位是通过生物信息学、抗体-登革热复合物三维结构分析、诱变/丙氨酸扫描和逃逸突变研究等方法确定的。此外,本文还综述了针对登革热E蛋白的单克隆抗体的治疗潜力。这可以为设计未来的登革热治疗方法提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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