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 PMID:33594366  

Adjuvanting a subunit SARS-CoV-2 nanoparticle vaccine to induce protective immunity in non-human primates.

Prabhu S Arunachalam | Alexandra C Walls | Nadia Golden | Caroline Atyeo | Stephanie Fischinger | Chunfeng Li | Pyone Aye | Mary Jane Navarro | Lilin Lai | Venkata Viswanadh Edara | Katharina Roltgen | Kenneth Rogers | Lisa Shirreff | Douglas E Ferrell | Samuel Wrenn | Deleah Pettie | John C Kraft | Marcos C Miranda | Elizabeth Kepl | Claire Sydeman | Natalie Brunette | Michael Murphy | Brooke Fiala | Lauren Carter | Alexander G White | Meera Trisal | Ching-Lin Hsieh | Kasi Russell-Lodrigue | Christopher Monjure | Jason Dufour | Lara Doyle-Meyer | Rudolph B Bohm | Nicholas J Maness | Chad Roy | Jessica A Plante | Kenneth S Plante | Alex Zhu | Matthew J Gorman | Sally Shin | Xiaoying Shen | Jane Fontenot | Shakti Gupta | Derek T O Hagan | Robbert Van Der Most | Rino Rappuoli | Robert L Coffman | David Novack | Jason S McLellan | Shankar Subramaniam | David Montefiori | Scott D Boyd | JoAnne L Flynn | Galit Alter | Francois Villinger | Harry Kleanthous | Jay Rappaport | Mehul Suthar | Neil P King | David Veesler | Bali Pulendran
bioRxiv : the preprint server for biology | 2021

The development of a portfolio of SARS-CoV-2 vaccines to vaccinate the global population remains an urgent public health imperative. Here, we demonstrate the capacity of a subunit vaccine under clinical development, comprising the SARS-CoV-2 Spike protein receptor-binding domain displayed on a two-component protein nanoparticle (RBD-NP), to stimulate robust and durable neutralizing antibody (nAb) responses and protection against SARS-CoV-2 in non-human primates. We evaluated five different adjuvants combined with RBD-NP including Essai O/W 1849101, a squalene-in-water emulsion; AS03, an alpha-tocopherol-containing squalene-based oil-in-water emulsion used in pandemic influenza vaccines; AS37, a TLR-7 agonist adsorbed to Alum; CpG 1018-Alum (CpG-Alum), a TLR-9 agonist formulated in Alum; or Alum, the most widely used adjuvant. All five adjuvants induced substantial nAb and CD4 T cell responses after two consecutive immunizations. Durable nAb responses were evaluated for RBD-NP/AS03 immunization and the live-virus nAb response was durably maintained up to 154 days post-vaccination. AS03, CpG-Alum, AS37 and Alum groups conferred significant protection against SARS-CoV-2 infection in the pharynges, nares and in the bronchoalveolar lavage. The nAb titers were highly correlated with protection against infection. Furthermore, RBD-NP when used in conjunction with AS03 was as potent as the prefusion stabilized Spike immunogen, HexaPro. Taken together, these data highlight the efficacy of the RBD-NP formulated with clinically relevant adjuvants in promoting robust immunity against SARS-CoV-2 in non-human primates.

Pubmed ID: 33594366

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Associated grants

  • Agency: NIH HHS, United States
    Id: P51 OD011104

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Tulane National Primate Research Center (tool)

RRID:SCR_008167

Center focused on understanding human health problems, including infectious diseases that require the use of nonhuman primates to develop diagnostics, therapeutics and preventive strategies. Primary research interests include developing vaccines, treatments and diagnostic tools for infectious diseases such as AIDS, tuberculosis, CMV, COVID-19, Lyme disease, and malaria. TNPRC has both biosafety level 2 and biosafety level 3 laboratories facilities to accommodate various research needs, and is the only National Primate Research Center with Regional Biosafety Laboratory.

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