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新冠疫情和疫苗更新:挑战与解决方案。

COVID-19 Pandemic and Vaccines Update on Challenges and Resolutions.

机构信息

Department of Biotechnology, Host Pathogen Interaction and Molecular Immunology Laboratory, Jamia Hamdard, New Delhi, India.

Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India.

出版信息

Front Cell Infect Microbiol. 2021 Sep 10;11:690621. doi: 10.3389/fcimb.2021.690621. eCollection 2021.

Abstract

The coronavirus disease (COVID-19) is caused by a positive-stranded RNA virus called severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), belonging to the family. This virus originated in Wuhan City, China, and became the cause of a multiwave pandemic that has killed 3.46 million people worldwide as of May 22, 2021. The havoc intensified with the emergence of SARS-CoV-2 variants (B.1.1.7; Alpha, B.1.351; Beta, P.1; Gamma, B.1.617; Delta, B.1.617.2; Delta-plus, B.1.525; Eta, and B.1.429; Epsilon etc.) due to mutations generated during replication. More variants may emerge to cause additional pandemic waves. The most promising approach for combating viruses and their emerging variants lies in prophylactic vaccines. Several vaccine candidates are being developed using various platforms, including nucleic acids, live attenuated virus, inactivated virus, viral vectors, and protein-based subunit vaccines. In this unprecedented time, 12 vaccines against SARS-CoV-2 have been phased in following WHO approval, 184 are in the preclinical stage, and 100 are in the clinical development process. Many of them are directed to elicit neutralizing antibodies against the viral spike protein (S) to inhibit viral entry through the ACE-2 receptor of host cells. Inactivated vaccines, to the contrary, provide a wide range of viral antigens for immune activation. Being an intracellular pathogen, the cytotoxic CD8 T Cell (CTL) response remains crucial for all viruses, including SARS-CoV-2, and needs to be explored in detail. In this review, we try to describe and compare approved vaccines against SARS-CoV-2 that are currently being distributed either after phase III clinical trials or for emergency use. We discuss immune responses induced by various candidate vaccine formulations; their benefits, potential limitations, and effectiveness against variants; future challenges, such as antibody-dependent enhancement (ADE); and vaccine safety issues and their possible resolutions. Most of the current vaccines developed against SARS-CoV-2 are showing either promising or compromised efficacy against new variants. Multiple antigen-based vaccines (multivariant vaccines) should be developed on different platforms to tackle future variants. Alternatively, recombinant BCG, containing SARS-CoV-2 multiple antigens, as a live attenuated vaccine should be explored for long-term protection. Irrespective of their efficacy, all vaccines are efficient in providing protection from disease severity. We must insist on vaccine compliance for all age groups and work on vaccine hesitancy globally to achieve herd immunity and, eventually, to curb this pandemic.

摘要

新型冠状病毒病(COVID-19)是由一种称为严重急性呼吸系统综合症冠状病毒 2 型(SARS-CoV-2)的正链 RNA 病毒引起的,属于 。该病毒源自中国武汉市,已成为多波大流行的病因,截至 2021 年 5 月 22 日,已导致全球 346 万人死亡。随着 SARS-CoV-2 变体(B.1.1.7;Alpha、B.1.351;Beta、P.1;Gamma、B.1.617;Delta、B.1.617.2;Delta-plus、B.1.525;Eta 和 B.1.429;Epsilon 等)因复制过程中产生的突变而出现,这种破坏加剧了。由于突变,可能会出现更多的变体来引发额外的大流行浪潮。对抗病毒及其新兴变体最有希望的方法是预防疫苗。正在使用各种平台开发几种疫苗候选物,包括核酸、减毒活病毒、灭活病毒、病毒载体和基于蛋白质的亚单位疫苗。在这个前所未有的时代,有 12 种针对 SARS-CoV-2 的疫苗已获得世卫组织批准,184 种处于临床前阶段,100 种处于临床开发过程中。其中许多旨在诱导针对病毒刺突蛋白(S)的中和抗体,以抑制病毒通过宿主细胞的 ACE-2 受体进入。相反,灭活疫苗为免疫激活提供了广泛的病毒抗原。作为细胞内病原体,细胞毒性 CD8 T 细胞(CTL)反应对所有病毒(包括 SARS-CoV-2)仍然至关重要,需要详细研究。在这篇综述中,我们试图描述和比较目前正在进行的针对 SARS-CoV-2 的已批准疫苗,这些疫苗要么已经完成 III 期临床试验,要么正在紧急使用中。我们讨论了各种候选疫苗制剂诱导的免疫反应;它们的益处、潜在局限性和对变体的有效性;未来的挑战,如抗体依赖性增强(ADE);以及疫苗安全性问题及其可能的解决方案。目前针对 SARS-CoV-2 开发的大多数疫苗对新变体的疗效要么有希望,要么受到限制。应在不同平台上开发多种抗原疫苗(多变体疫苗)以应对未来的变体。或者,作为减毒活疫苗,含有 SARS-CoV-2 多种抗原的重组卡介苗也应该被探索用于长期保护。无论其疗效如何,所有疫苗在预防疾病严重程度方面都非常有效。我们必须坚持为所有年龄段的人接种疫苗,并在全球范围内解决疫苗犹豫问题,以实现群体免疫,并最终遏制这一大流行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7aa0/8461057/40db694868a2/fcimb-11-690621-g001.jpg

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