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Sterilizing Immunity against SARS-CoV-2 Infection in Mice by a Single-Shot and Lipid Amphiphile Imidazoquinoline TLR7/8 Agonist-Adjuvanted Recombinant Spike Protein Vaccine*. | LitMetric

AI Article Synopsis

  • Scientists are racing to develop vaccines against SARS-CoV-2 to reduce severe illness and death from COVID-19.
  • The study introduces an innovative adjuvant, IMDQ-PEG-CHOL, which enhances immune response and targets lymph nodes effectively while minimizing systemic inflammation.
  • Testing showed that this adjuvant significantly improved antibody production and neutralizing capabilities against the virus in mouse models, demonstrating its potential for use in COVID-19 vaccines.

Article Abstract

The search for vaccines that protect from severe morbidity and mortality because of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19) is a race against the clock and the virus. Here we describe an amphiphilic imidazoquinoline (IMDQ-PEG-CHOL) TLR7/8 adjuvant, consisting of an imidazoquinoline conjugated to the chain end of a cholesterol-poly(ethylene glycol) macromolecular amphiphile. It is water-soluble and exhibits massive translocation to lymph nodes upon local administration through binding to albumin, affording localized innate immune activation and reduction in systemic inflammation. The adjuvanticity of IMDQ-PEG-CHOL was validated in a licensed vaccine setting (quadrivalent influenza vaccine) and an experimental trimeric recombinant SARS-CoV-2 spike protein vaccine, showing robust IgG2a and IgG1 antibody titers in mice that could neutralize viral infection in vitro and in vivo in a mouse model.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8014308PMC
http://dx.doi.org/10.1002/anie.202015362DOI Listing

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