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10.1186/s12934-021-01584-5

http://scihub22266oqcxt.onion/10.1186/s12934-021-01584-5
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suck abstract from ncbi


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pmid33952256      Microb+Cell+Fact 2021 ; 20 (1): 95
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  • Immune response induced by oral administration with a Saccharomyces cerevisiae-based SARS-CoV-2 vaccine in mice #MMPMID33952256
  • Gao T; Ren Y; Li S; Lu X; Lei H
  • Microb Cell Fact 2021[May]; 20 (1): 95 PMID33952256show ga
  • BACKGROUND: The global pandemic of coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) highlights the need to develop safe and effective vaccines with a top priority. Multiple vaccine candidates are under development, and several vaccines are currently available. Efforts need to be undertaken to counter the threat of the global COVID-19 pandemic. RESULTS: We generated a Saccharomyces cerevisiae (S. cerevisiae)-based SARS-CoV-2 vaccine, EBY100/pYD1-RBD, in which the full-length receptor binding domain (RBD) of the spike protein of SARS-CoV-2 was expressed on the surface of yeast. Mice vaccinated orally with unadjuvanted EBY100/pYD1-RBD could produce significant humoral and mucosal responses as well as robust cellular immune responses. Notably, EBY100/pYD1-RBD elicited a mixed Th1/Th2-type cellular immune response with a Th1-biased immune response in a mouse model. CONCLUSIONS: Our findings highlight the importance of the RBD as a key target to design and develop vaccines against SARS-CoV-2 and provide evidence of oral administration of a S. cerevisiae-based SARS-CoV-2 vaccine eliciting significant immune responses. Most importantly, the S. cerevisiae surface display system can serve as a universal technology platform and be applied to develop other oral viral or bacterial vaccines.
  • |*Immunity, Cellular[MESH]
  • |*Saccharomyces cerevisiae[MESH]
  • |Administration, Oral[MESH]
  • |Animals[MESH]
  • |Binding Sites[MESH]
  • |COVID-19 Vaccines/administration & dosage/*immunology[MESH]
  • |COVID-19/*immunology/prevention & control[MESH]
  • |Female[MESH]
  • |Immunity, Humoral[MESH]
  • |Immunity, Mucosal[MESH]
  • |Mice[MESH]
  • |Mice, Inbred BALB C[MESH]


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