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10.1126/scitranslmed.abg1143

http://scihub22266oqcxt.onion/10.1126/scitranslmed.abg1143
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suck abstract from ncbi


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pmid34285130      Sci+Transl+Med 2021 ; 13 (606): ä
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  • A recombinant spike protein subunit vaccine confers protective immunity against SARS-CoV-2 infection and transmission in hamsters #MMPMID34285130
  • Wu Y; Huang X; Yuan L; Wang S; Zhang Y; Xiong H; Chen R; Ma J; Qi R; Nie M; Xu J; Zhang Z; Chen L; Wei M; Zhou M; Cai M; Shi Y; Zhang L; Yu H; Hong J; Wang Z; Hong Y; Yue M; Li Z; Chen D; Zheng Q; Li S; Chen Y; Cheng T; Zhang J; Zhang T; Zhu H; Zhao Q; Yuan Q; Guan Y; Xia N
  • Sci Transl Med 2021[Aug]; 13 (606): ä PMID34285130show ga
  • Multiple safe and effective vaccines that elicit immune responses against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are necessary to respond to the ongoing coronavirus disease 2019 (COVID-19) pandemic. Here, we developed a protein subunit vaccine composed of spike ectodomain protein (StriFK) plus a nitrogen bisphosphonate-modified zinc-aluminum hybrid adjuvant (FH002C). StriFK-FH002C generated substantially higher neutralizing antibody titers in mice, hamsters, and cynomolgus monkeys than those observed in plasma isolated from COVID-19 convalescent individuals. StriFK-FH002C also induced both T(H)1- and T(H)2-polarized helper T cell responses in mice. In hamsters, StriFK-FH002C immunization protected animals against SARS-CoV-2 challenge, as shown by the absence of virus-induced weight loss, fewer symptoms of disease, and reduced lung pathology. Vaccination of hamsters with StriFK-FH002C also reduced within-cage virus transmission to unvaccinated, cohoused hamsters. In summary, StriFK-FH002C represents an effective, protein subunit-based SARS-CoV-2 vaccine candidate.
  • |*COVID-19[MESH]
  • |Animals[MESH]
  • |Antibodies, Neutralizing[MESH]
  • |Antibodies, Viral[MESH]
  • |COVID-19 Vaccines[MESH]
  • |Cricetinae[MESH]
  • |Humans[MESH]
  • |Mice[MESH]
  • |Protein Subunits[MESH]
  • |SARS-CoV-2[MESH]


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