Carbohydrate fatty acid monosulphate: oil-in-water adjuvant enhances SARS-CoV-2 RBD nanoparticle-induced immunogenicity and protection in mice

Author:

Nanishi EtsuroORCID,Borriello Francesco,Seo Hyuk-SooORCID,O’Meara Timothy R.ORCID,McGrath Marisa E.,Saito Yoshine,Chen Jing,Diray-Arce Joann,Song KijunORCID,Xu Andrew Z.ORCID,Barman SoumikORCID,Menon Manisha,Dong DanicaORCID,Caradonna Timothy M.,Feldman Jared,Hauser Blake M.ORCID,Schmidt Aaron G.,Baden Lindsey R.,Ernst Robert K.ORCID,Dillen Carly,Yu Jingyou,Chang Aiquan,Hilgers Luuk,Platenburg Peter PaulORCID,Dhe-Paganon Sirano,Barouch Dan H.ORCID,Ozonoff AlORCID,Zanoni Ivan,Frieman Matthew B.ORCID,Dowling David J.ORCID,Levy OferORCID

Abstract

AbstractDevelopment of SARS-CoV-2 vaccines that protect vulnerable populations is a public health priority. Here, we took a systematic and iterative approach by testing several adjuvants and SARS-CoV-2 antigens to identify a combination that elicits antibodies and protection in young and aged mice. While demonstrating superior immunogenicity to soluble receptor-binding domain (RBD), RBD displayed as a protein nanoparticle (RBD-NP) generated limited antibody responses. Comparison of multiple adjuvants including AddaVax, AddaS03, and AS01B in young and aged mice demonstrated that an oil-in-water emulsion containing carbohydrate fatty acid monosulphate derivative (CMS:O/W) most effectively enhanced RBD-NP-induced cross-neutralizing antibodies and protection across age groups. CMS:O/W enhanced antigen retention in the draining lymph node, induced injection site, and lymph node cytokines, with CMS inducing MyD88-dependent Th1 cytokine polarization. Furthermore, CMS and O/W synergistically induced chemokine production from human PBMCs. Overall, CMS:O/W adjuvant may enhance immunogenicity and protection of vulnerable populations against SARS-CoV-2 and other infectious pathogens.

Funder

U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases

Massachusetts Consortium on Pathogenesis Readiness

U.S. Department of Health & Human Services | National Institutes of Health

U.S. Department of Health & Human Services | Biomedical Advanced Research and Development Authority

United States Department of Defense | Defense Advanced Research Projects Agency

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Infectious Diseases,Pharmacology,Immunology

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