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1
Human rhinoviruses prevailed among children in the setting of wearing face masks in Shanghai, 2020.2020年在上海,佩戴口罩的情况下,人鼻病毒在儿童中占主导地位。
BMC Infect Dis. 2022 Mar 14;22(1):253. doi: 10.1186/s12879-022-07225-5.
2
Immuno-informatics analysis predicts B and T cell consensus epitopes for designing peptide vaccine against SARS-CoV-2 with 99.82% global population coverage.免疫信息学分析预测了针对 SARS-CoV-2 的肽疫苗设计的 B 和 T 细胞共识表位,可覆盖全球 99.82%的人口。
Brief Bioinform. 2022 Jan 17;23(1). doi: 10.1093/bib/bbab496.
3
Incidence and Outcome of Coinfections with SARS-CoV-2 and Rhinovirus.SARS-CoV-2 与鼻病毒合并感染的发生率和结局。
Viruses. 2021 Dec 16;13(12):2528. doi: 10.3390/v13122528.
4
Severe Acute Respiratory Syndrome Coronavirus 2 and Respiratory Virus Sentinel Surveillance, California, USA, May 10, 2020-June 12, 2021.2020 年 5 月 10 日至 2021 年 6 月 12 日,美国加利福尼亚州严重急性呼吸综合征冠状病毒 2 型和呼吸道病毒哨点监测。
Emerg Infect Dis. 2022 Jan;28(1):9-19. doi: 10.3201/eid2801.211682.
5
Comparing COVID-19 vaccines for their characteristics, efficacy and effectiveness against SARS-CoV-2 and variants of concern: a narrative review.比较 COVID-19 疫苗在针对 SARS-CoV-2 及其关注变异株的特性、疗效和有效性方面的差异:一项叙述性综述。
Clin Microbiol Infect. 2022 Feb;28(2):202-221. doi: 10.1016/j.cmi.2021.10.005. Epub 2021 Oct 27.
6
Prevalence and outcomes of co-infection and superinfection with SARS-CoV-2 and other pathogens: A systematic review and meta-analysis.SARS-CoV-2 与其他病原体合并感染和继发感染的流行率和结局:系统评价和荟萃分析。
PLoS One. 2021 May 6;16(5):e0251170. doi: 10.1371/journal.pone.0251170. eCollection 2021.
7
Human Rhinovirus Infection Blocks Severe Acute Respiratory Syndrome Coronavirus 2 Replication Within the Respiratory Epithelium: Implications for COVID-19 Epidemiology.人类鼻病毒感染可阻断呼吸道上皮细胞中的严重急性呼吸综合征冠状病毒 2 复制:对 COVID-19 流行病学的启示。
J Infect Dis. 2021 Jul 2;224(1):31-38. doi: 10.1093/infdis/jiab147.
8
Increased risk of rhinovirus infection in children during the coronavirus disease-19 pandemic.新冠疫情期间儿童感染鼻病毒的风险增加。
Influenza Other Respir Viruses. 2021 Jul;15(4):488-494. doi: 10.1111/irv.12854. Epub 2021 Mar 14.
9
COVID-19 vaccine: A recent update in pipeline vaccines, their design and development strategies.COVID-19 疫苗:管道疫苗的最新更新、设计和开发策略。
Eur J Pharmacol. 2021 Feb 5;892:173751. doi: 10.1016/j.ejphar.2020.173751. Epub 2020 Nov 25.
10
Human rhinovirus-specific CD8 T cell responses target conserved and unusual epitopes.人鼻病毒特异性 CD8 T 细胞应答针对保守和非保守表位。
FASEB J. 2021 Jan;35(1):e21208. doi: 10.1096/fj.202002165R. Epub 2020 Nov 23.

将普通感冒改造为活减毒 SARS-CoV-2 疫苗。

Engineering the common cold to be a live-attenuated SARS-CoV-2 vaccine.

机构信息

Department of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.

出版信息

Front Immunol. 2022 Sep 8;13:871463. doi: 10.3389/fimmu.2022.871463. eCollection 2022.

DOI:10.3389/fimmu.2022.871463
PMID:36189239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9516391/
Abstract

According to the American Centers for Disease Control and Prevention, people in all age groups catch two or more "colds" per year, at least half of which are caused by human rhinoviruses. Despite decades of effort, there are no vaccines or drugs against rhinovirus infections and even social distancing measures that were effective in reducing the spread of the pandemic coronavirus, SARS-CoV-2, did not reduce the rate of rhinovirus detection. Fortunately, most rhinovirus strains are naturally attenuated in that they are not associated with serious illness, hospitalization or mortality. Instead, rhinoviruses are one of the most frequent viruses found in nasal swabs of asymptomatic, healthy people. Since rhinovirus infections cannot be avoided, a rational approach would be to engineer them for the benefit of their human hosts. Rhinovirus infections naturally induce robust mucosal and serum immune responses to all virus-expressed proteins. Several replication-competent, human rhinovirus vaccine vectors able to express protective antigens for other pathogens have already been designed and tested in animal models. With this strategy, the inevitable common cold would be able to induce immunity not just to a specific rhinovirus serotype but to other more pathogenic respiratory viruses as well. This article reviews existing rhinovirus vaccine vector technology and describes the characteristics that make live-attenuated rhinoviruses attractive vaccine candidates for SARS-CoV-2 and other pathogenic respiratory viruses in the future.

摘要

根据美国疾病控制与预防中心的数据,所有年龄段的人每年都会感染两到两种以上的“感冒”,其中至少有一半是由人类鼻病毒引起的。尽管经过了几十年的努力,目前仍然没有针对鼻病毒感染的疫苗或药物,甚至在大流行冠状病毒 SARS-CoV-2 传播期间有效的社交距离措施,也没有降低鼻病毒的检出率。幸运的是,大多数鼻病毒株在自然状态下会减弱,它们不会导致严重疾病、住院或死亡。相反,鼻病毒是在无症状、健康人群的鼻腔拭子中发现的最常见的病毒之一。由于无法避免鼻病毒感染,因此一种合理的方法是将其用于造福人类宿主。鼻病毒感染会自然诱导针对所有病毒表达蛋白的强大黏膜和血清免疫反应。已经设计并在动物模型中测试了几种能够表达其他病原体保护性抗原的复制型、人类鼻病毒疫苗载体。通过这种策略,不可避免的普通感冒将不仅能够诱导针对特定鼻病毒血清型的免疫,还能够诱导针对其他更具致病性的呼吸道病毒的免疫。本文综述了现有的鼻病毒疫苗载体技术,并描述了使减毒鼻病毒成为 SARS-CoV-2 和未来其他致病性呼吸道病毒有吸引力的疫苗候选物的特征。