SARS-CoV-2 vaccines elicit durable immune responses in infant rhesus macaques.

Journal Article (Journal Article)

The inclusion of infants in the SARS-CoV-2 vaccine roll-out is important to prevent severe complications of pediatric SARS-CoV-2 infections and to limit transmission and could possibly be implemented via the global pediatric vaccine schedule. However, age-dependent differences in immune function require careful evaluation of novel vaccines in the pediatric population. Toward this goal, we assessed the safety and immunogenicity of two SARS-CoV-2 vaccines. Two groups of 8 infant rhesus macaques (RMs) were immunized intramuscularly at weeks 0 and 4 with stabilized prefusion SARS-CoV-2 S-2P spike (S) protein encoded by mRNA encapsulated in lipid nanoparticles (mRNA-LNP) or the purified S protein mixed with 3M-052, a synthetic TLR7/8 agonist in a squalene emulsion (Protein+3M-052-SE). Neither vaccine induced adverse effects. Both vaccines elicited high magnitude IgG binding to RBD, N terminus domain, S1, and S2, ACE2 blocking activity, and high neutralizing antibody titers, all peaking at week 6. S-specific memory B cells were detected by week 4 and S-specific T cell responses were dominated by the production of IL-17, IFN-γ, or TNF-α. Antibody and cellular responses were stable through week 22. The immune responses for the mRNA-LNP vaccine were of a similar magnitude to those elicited by the Moderna mRNA-1273 vaccine in adults. The S-2P mRNA-LNP and Protein-3M-052-SE vaccines were well-tolerated and highly immunogenic in infant RMs, providing proof-of concept for a pediatric SARS-CoV-2 vaccine with the potential for durable immunity that might decrease the transmission of SARS-CoV-2 and mitigate the ongoing health and socioeconomic impacts of COVID-19.

Full Text

Duke Authors

Cited Authors

  • Garrido, C; Curtis, AD; Dennis, M; Pathak, SH; Gao, H; Montefiori, D; Tomai, M; Fox, CB; Kozlowski, PA; Scobey, T; Munt, JE; Mallory, ML; Saha, PT; Hudgens, MG; Lindesmith, LC; Baric, RS; Abiona, OM; Graham, B; Corbett, KS; Edwards, D; Carfi, A; Fouda, G; Van Rompay, KKA; De Paris, K; Permar, SR

Published Date

  • June 2021

Published In

Volume / Issue

  • 6 / 60

PubMed ID

  • 34131024

Electronic International Standard Serial Number (EISSN)

  • 2470-9468

International Standard Serial Number (ISSN)

  • 2470-9468

Digital Object Identifier (DOI)

  • 10.1126/sciimmunol.abj3684


  • eng