Vaccination against SARS-CoV-2 using extracellular blebs derived from spike protein-expressing dendritic cells
Cellular Immunology, ISSN: 0008-8749, Vol: 386, Page: 104691
2023
- 4Citations
- 10Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations4
- Citation Indexes4
- Captures10
- Readers10
- 10
Article Description
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.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0008874923000308; http://dx.doi.org/10.1016/j.cellimm.2023.104691; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85148677284&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/36822152; https://linkinghub.elsevier.com/retrieve/pii/S0008874923000308; https://dx.doi.org/10.1016/j.cellimm.2023.104691
Elsevier BV
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