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The investigation of mRNA vaccines formulated in liposomes administrated in multiple routes against SARS-CoV-2.

Abstract
COVID-19 pandemic has resulted in an unprecedented global public health crisis. It is obvious that SARS-CoV-2 vaccine is needed to control the global COVID-19 public health crisis. Since obvious advantages including fast manufacturing speed, potent immunogenicity and good safety profile, six mRNA vaccines have been used to prevent SARS-CoV-2 infections in clinic with lipid nanoparticles (LNP) formulation via intramuscular injection. In this work, we first constructed RBD-encoding mRNA (RBD-mRNA) formulated in liposomes (LPX/RBD-mRNA) and investigated the influence of administration routes on the immunogenicity. LPX/RBD-mRNA can express RBD in vivo and successfully induced SARS-CoV-2 RBD specific antibodies in the vaccinated mice, which efficiently neutralized SARS-CoV-2 pseudotyped virus. Moreover, the administration routes were found to affect the virus neutralizing capacity of sera derived from the immunized mice and the types (Th1-type and Th2-type) of cellular immune responses. This study indicated that liposome-based RBD-mRNA vaccine with optimal administration route might be a potential candidate against SARS-CoV-2 infection with good efficacy and safety.
AuthorsHai Huang, Caili Zhang, Shuping Yang, Wen Xiao, Qian Zheng, Xiangrong Song
JournalJournal of controlled release : official journal of the Controlled Release Society (J Control Release) Vol. 335 Pg. 449-456 (07 10 2021) ISSN: 1873-4995 [Electronic] Netherlands
PMID34029632 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2021. Published by Elsevier B.V.
Chemical References
  • Antibodies, Neutralizing
  • Antibodies, Viral
  • COVID-19 Vaccines
  • Liposomes
  • RNA, Messenger
  • Spike Glycoprotein, Coronavirus
  • Vaccines
Topics
  • Animals
  • Antibodies, Neutralizing
  • Antibodies, Viral
  • COVID-19
  • COVID-19 Vaccines
  • Humans
  • Liposomes
  • Mice
  • Mice, Inbred BALB C
  • Pandemics
  • RNA, Messenger
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus
  • Vaccines

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