An Overview of Adenovirus Vector-based Vaccines against SARS-CoV-2

Q4 Veterinary
Gamil S. G. Zeedan, A. Abdalhamed, A. Naguib, S. Shalaby, Mona A. M. Awad, Mervat I. Abd El Moniem
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引用次数: 0

Abstract

Adenovirus vectors have been employed to develop a vaccine against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) for curtailing the Covid-19 pandemic spreading. Many different viral vectors have been mainly targeting the SARS-CoV-2 spike (S) protein as an antigen. Spike (S) protein is comprised of S1 and S2 subunits, in which the receptor-binding domain (RBD) of S1 is responsible for recognizing and engaging with its host cellular receptor protein angiotensin-converting enzyme 2 (ACE2), S2 accounts for membrane fusion of virus and host cell. Chimpanzee adenovirus was also used as a vector vaccine for SARS-CoV-2 (ChAdSARS-CoV-2-S) by intramuscular injection, and intranasal administration has been tested. Adenovirus vector-based vaccines are the most advanced, with several vaccines receiving Emergency Use Authorization (EUA). It was shown that rhesus macaques were protected from SARS-CoV-2 challenge after a month of being vaccinated with ChAd-SARS-CoV-2-S. A single intranasal or two intramuscular ChAd-SARSCoV-2-S vaccines could induce humoral antibodies and T cell responses to protect the upper and lower respiratory tract against SARS-CoV-2. As the effectiveness was demonstrated in non-human primates, ChAd-SARS-CoV-2-Sa potential option for preventing SARS-CoV-2 infection in humans. However, detecting novel more transmissible and pathogenic SARS-CoV-2 variants added concerns about the vaccine efficacy and needs monitoring. Moreover, the cause of recently documented rare cases of vaccine indicated immune thrombotic thrombocytopenia. This review article provided details for the adenovirus vector vaccine for SARS-CoV-2 in humans and tried to provide solutions to the adenovirus vector hemagglutinin issue.
基于腺病毒载体的严重急性呼吸系统综合征冠状病毒2型疫苗综述
腺病毒载体已被用于开发针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的疫苗,以遏制新冠肺炎大流行的传播。许多不同的病毒载体主要靶向作为抗原的严重急性呼吸系统综合征冠状病毒2型刺突蛋白。刺突蛋白由S1和S2亚基组成,其中S1的受体结合域(RBD)负责识别并与其宿主细胞受体蛋白血管紧张素转化酶2(ACE2)结合,S2负责病毒和宿主细胞的膜融合。黑猩猩腺病毒也通过肌肉注射被用作严重急性呼吸系统综合征冠状病毒2型(ChAd严重急性呼吸综合征冠状病毒2-S)的载体疫苗,并且鼻内给药已经过测试。腺病毒载体疫苗是最先进的,有几种疫苗获得了紧急使用授权(EUA)。研究表明,恒河猴在接种ChAd-SARS-CoV-2疫苗一个月后,可以免受严重急性呼吸系统综合征冠状病毒2型的攻击。单一的鼻内或两种肌肉注射ChAd-SARSCoV-2-S疫苗可以诱导体液抗体和T细胞反应,以保护上呼吸道和下呼吸道免受严重急性呼吸系统综合征冠状病毒2型的感染。正如在非人类灵长类动物中证明的有效性一样,ChAd-SARS-CoV-2是预防人类严重急性呼吸系统综合征冠状病毒2型感染的潜在选择。然而,检测到新的更具传播性和致病性的严重急性呼吸系统综合征冠状病毒2型变种增加了人们对疫苗效力的担忧,需要监测。此外,最近记录的罕见疫苗病例的原因表明免疫性血栓性血小板减少症。这篇综述文章提供了针对人类严重急性呼吸系统综合征冠状病毒2型的腺病毒载体疫苗的详细信息,并试图为腺病毒载体血凝素问题提供解决方案。
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
World''s Veterinary Journal
World''s Veterinary Journal Veterinary-Veterinary (all)
CiteScore
1.00
自引率
0.00%
发文量
43
期刊介绍: The World''s Veterinary Journal (ISSN 2322-4568) is an international, peer reviewed open access journal aims to publish the high quality material from veterinary scientists'' studies. All accepted articles are published Quarterly in full text on the Internet. WVJ publishes the results of original scientific researches, reviews, case reports and short communications, in all fields of veterinary science. In details, topics are: Behavior Environment and welfare Animal reproduction and production Parasitology Endocrinology Microbiology Immunology Pathology Pharmacology Epidemiology Molecular biology Immunogenetics Surgery Virology Physiology Vaccination Gynecology Exotic animals Animal diseases Radiology Ophthalmology Dermatology Chronic disease Anatomy Non-surgical pathology issues of small to large animals Cardiology and oncology.
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