4.8 Article

An aluminum hydroxide:CpG adjuvant enhances protection elicited by a SARS-CoV-2 receptor binding domain vaccine in aged mice

Journal

SCIENCE TRANSLATIONAL MEDICINE
Volume 14, Issue 629, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scitranslmed.abj5305

Keywords

-

Funding

  1. National Institutes of Health (NIH)/National Institutes of Allergy and Infectious Diseases (NIAID) [HHSN272201400052C, 75N93019C00044, HHSN272201800047C]
  2. Massachusetts Consortium on Pathogen Readiness (Mass-CPR) award
  3. NIH [1R21AI137932-01A1, R01 AI148166, HHSN272201400007C, R01 AI146779, 1R01AI121066, 1R01DK115217, 1R01AI165505]
  4. Adjuvant Discovery Program [75N93019C00044]
  5. U.S. Army's Long Term Health and Education Training Program [ASPR-20-01495]
  6. DARPA [ASPR-20-01495]
  7. MassCPR grant
  8. NIGMS [T32 GM007753, T32 AI007245]
  9. Lloyd J. Old STAR Program [CRI3888]
  10. Burroughs Wellcome Fund
  11. BCH Department of Pediatrics
  12. Chief Scientific Office
  13. Daiichi Sankyo Foundation of Life Science
  14. Uehara Memorial Foundation
  15. joint Society for Pediatric Research and Japanese Pediatric Society Scholar

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The global deployment of vaccines for COVID-19 is urgently needed, especially in low- and middle-income countries. The study found that a specific adjuvant formulation significantly increased neutralizing antibody levels and protected aged mice from SARS-CoV-2. These findings support the further development of this adjuvanted vaccine as an effective and affordable option.
Global deployment of vaccines that can provide protection across several age groups is still urgently needed to end the COVID-19 pandemic, especially in low- and middle-income countries. Although vaccines against SARSCoV-2 based on mRNA and adenoviral vector technologies have been rapidly developed, additional practical and scalable SARS-CoV-2 vaccines are required to meet global demand. Protein subunit vaccines formulated with appropriate adjuvants represent an approach to address this urgent need. The receptor binding domain (RBD) is a key target of SARS-CoV-2 neutralizing antibodies but is poorly immunogenic. We therefore compared pattern recognition receptor (PRR) agonists alone or formulated with aluminum hydroxide (AH) and benchmarked them against AS01 B and AS03-like emulsion-based adjuvants for their potential to enhance RBD immunogenicity in young and aged mice. We found that an AH and CpG adjuvant formulation (AH:CpG) produced an 80-fold increase in anti-RBD neutralizing antibody titers in both age groups relative to AH alone and protected aged mice from the SARS-CoV-2 challenge. The AH:CpG-adjuvanted RBD vaccine elicited neutralizing antibodies against both wild-type SARS-CoV-2 and the B.1.351 (beta) variant at serum concentrations comparable to those induced by the licensed Pfizer-BioNTech BNT162b2 mRNA vaccine. AH:CpG induced similar cytokine and chemokine gene enrichment patterns in the draining lymph nodes of both young adult and aged mice and enhanced cytokine and chemokine production in human mononuclear cells of younger and older adults. These data support further development of AH:CpG-adjuvanted RBD as an affordable vaccine that may be effective across multiple age groups.

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