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Vaccination against SARS-CoV-2 using extracellular blebs derived from spike protein-expressing dendritic cells.
Young Chung, Jee; Thone, Melissa N; Davies, Jenny E; Gach, Johannes S; Huw Davies, D; Forthal, Donald N; Kwon, Young Jik.
Affiliation
  • Young Chung J; Department of Pharmaceutical Sciences, University of California, Irvine, CA 92697, United States.
  • Thone MN; Department of Pharmaceutical Sciences, University of California, Irvine, CA 92697, United States.
  • Davies JE; Vaccine Research and Development Center, Department of Physiology and Biophysics, University of California, Irvine, CA 92697, United States.
  • Gach JS; Division of Infectious Diseases, Department of Medicine, University of California, Irvine, CA 92697, United States.
  • Huw Davies D; Vaccine Research and Development Center, Department of Physiology and Biophysics, University of California, Irvine, CA 92697, United States.
  • Forthal DN; Division of Infectious Diseases, Department of Medicine, University of California, Irvine, CA 92697, United States.
  • Kwon YJ; Department of Pharmaceutical Sciences, University of California, Irvine, CA 92697, United States; Department of Chemical and Biomolecular Engineering, University of California, Irvine, CA 92697, United States; Department of Biomedical Engineering, University of California, Irvine, CA 92697, United S
Cell Immunol ; 386: 104691, 2023 04.
Article in En | MEDLINE | ID: mdl-36822152
ABSTRACT
COVID-19 has caused significant morbidity and mortality worldwide but also accelerated the clinical use of emerging vaccine formulations. To address the current shortcomings in the prevention and treatment of SARS-CoV-2 infection, this study developed a novel vaccine platform that closely mimics dendritic cells (DCs) in antigen presentation and T-cell stimulation in a cell-free and tunable manner. Genetically engineered DCs that express the SARS-CoV-2 spike protein (S) were chemically converted into extracellular blebs (EBs). The resulting EBs elicited potentially protective humoral immunity in vivo, indicated by the production of antibodies that potently neutralized S-pseudotyped virus, presenting EBs as a promising and safe vaccine.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: Cell Immunol Year: 2023 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Limits: Humans Language: En Journal: Cell Immunol Year: 2023 Document type: Article Affiliation country: Estados Unidos