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10.1021/acs.nanolett.1c01284

http://scihub22266oqcxt.onion/10.1021/acs.nanolett.1c01284
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34032435!ä!34032435

suck abstract from ncbi


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pmid34032435      Nano+Lett 2021 ; 21 (11): 4774-4779
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  • Lipid Nanoparticle RBD-hFc mRNA Vaccine Protects hACE2 Transgenic Mice against a Lethal SARS-CoV-2 Infection #MMPMID34032435
  • Elia U; Rotem S; Bar-Haim E; Ramishetti S; Naidu GS; Gur D; Aftalion M; Israeli M; Bercovich-Kinori A; Alcalay R; Makdasi E; Chitlaru T; Rosenfeld R; Israely T; Melamed S; Abutbul Ionita I; Danino D; Peer D; Cohen O
  • Nano Lett 2021[Jun]; 21 (11): 4774-4779 PMID34032435show ga
  • The COVID-19 pandemic led to development of mRNA vaccines, which became a leading anti-SARS-CoV-2 immunization platform. Preclinical studies are limited to infection-prone animals such as hamsters and monkeys in which protective efficacy of vaccines cannot be fully appreciated. We recently reported a SARS-CoV-2 human Fc-conjugated receptor-binding domain (RBD-hFc) mRNA vaccine delivered via lipid nanoparticles (LNPs). BALB/c mice demonstrated specific immunologic responses following RBD-hFc mRNA vaccination. Now, we evaluated the protective effect of this RBD-hFc mRNA vaccine by employing the K18 human angiotensin-converting enzyme 2 (K18-hACE2) mouse model. Administration of an RBD-hFc mRNA vaccine to K18-hACE2 mice resulted in robust humoral responses comprising binding and neutralizing antibodies. In correlation with this response, 70% of vaccinated mice withstood a lethal SARS-CoV-2 dose, while all control animals succumbed to infection. To the best of our knowledge, this is the first nonreplicating mRNA vaccine study reporting protection of K18-hACE2 against a lethal SARS-CoV-2 infection.
  • |*COVID-19[MESH]
  • |*Nanoparticles[MESH]
  • |*Vaccines[MESH]
  • |Animals[MESH]
  • |Humans[MESH]
  • |Lipids[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]
  • |Mice, Transgenic[MESH]
  • |Pandemics[MESH]
  • |RNA, Messenger/genetics[MESH]
  • |SARS-CoV-2[MESH]


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