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Campo DC | Valor | Idioma |
---|---|---|
dc.creator | Zhang, Na-Na | - |
dc.creator | Li, Xiao-Feng | - |
dc.creator | Deng, Yong-Qiang | - |
dc.creator | Zhao, Hui | - |
dc.creator | Huang, Yi-Jiao | - |
dc.creator | Yang, Guan | - |
dc.creator | Huang, Wei-Jin | - |
dc.creator | Gao, Peng | - |
dc.creator | Zhou, Chao | - |
dc.creator | Zhang, Rong-Rong | - |
dc.creator | Guo, Yan | - |
dc.creator | Sun, Shi-Hui | - |
dc.creator | Fan, Hang | - |
dc.creator | Zu, Shu-Long | - |
dc.creator | Chen, Qi | - |
dc.creator | He, Qi | - |
dc.creator | Cao, Tian-Shu | - |
dc.creator | Huang, Xing-Yao | - |
dc.creator | Qiu, Hong-Ying | - |
dc.creator | Nie, Jian-Hui | - |
dc.creator | Jiang, Yuhang | - |
dc.creator | Yan, Hua-Yuan | - |
dc.creator | Ye, Qing | - |
dc.creator | Zhong, Xia | - |
dc.creator | Xue, Xia-Lin | - |
dc.creator | Zha, Zhen-Yu | - |
dc.creator | Zhou, Dongsheng | - |
dc.creator | Yang, Xiao | - |
dc.creator | Wang, You-Chun | - |
dc.creator | Ying, Bo | - |
dc.creator | Qin, Cheng-Feng | - |
dc.date.accessioned | 2020-08-03T13:19:54Z | - |
dc.date.available | 2020-08-03T13:19:54Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | ZHANG, N.-N. et al. A thermostable mRNA vaccine against COVID-19. Cell, [S.l.], 2020. No prelo. | pt_BR |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0092867420309326 | pt_BR |
dc.identifier.uri | http://repositorio.ufla.br/jspui/handle/1/42179 | - |
dc.description.abstract | There has been an urgent need of vaccines against coronavirus disease 2019 (COVID-19) due to the ongoing SARS-CoV-2 pandemic. Among all approaches, messenger RNA (mRNA) -based vaccine has emerged as a rapid and versatile platform to quickly respond to such a challenge. Here, we developed a lipid-nanoparticle-encapsulated mRNA (mRNA-LNP) encoding the receptor binding domain (RBD) of SARS-CoV-2 as a vaccine candidate (termed ARCoV). Intramuscular immunization of ARCoV mRNA-LNPs elicited robust neutralizing antibodies against SARS-CoV-2 as well as Th1-biased cellular response in mice and non-human primates. Two doses of ARCoV immunization in mice conferred complete protection against the challenge of a SARS-CoV-2 mouse adapted strain. Additionally, ARCoV was manufactured in liquid formulation and can be stored at room temperature for at least one week. This novel COVID-19 mRNA vaccine, ARCoV, is currently being evaluated in phase 1 clinical trials. | pt_BR |
dc.language | en_US | pt_BR |
dc.publisher | Elsevier | pt_BR |
dc.rights | restrictAccess | pt_BR |
dc.source | Cell | pt_BR |
dc.subject | Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) | pt_BR |
dc.subject | COVID-19 | pt_BR |
dc.subject | mRNA vaccine | pt_BR |
dc.subject | Lipid nanoparticle | pt_BR |
dc.subject | Mouse adapted strain | pt_BR |
dc.subject | Non-human primate | pt_BR |
dc.title | A thermostable mRNA vaccine against COVID-19 | pt_BR |
dc.type | Artigo | pt_BR |
Aparece nas coleções: | FCS - Artigos sobre Coronavirus Disease 2019 (COVID-19) |
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