CD8 T cells contribute to vaccine protection against SARS-CoV-2 in macaques
Open accessAbstract
Spike-specific neutralizing antibodies (NAbs) are generally considered key correlates of vaccine protection against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Recently, robust vaccine prevention of severe disease with SARS-CoV-2 variants that largely escape NAb responses has been reported, suggesting a role for other immune parameters for virologic control. However, direct data demonstrating a role of CD8 + T cells in vaccine protection have not yet been reported. In this study, we show that vaccine-elicited CD8 + T cells contribute substantially to virologic control after SARS-CoV-2 challenge in rhesus macaques. We vaccinated 30 macaques with a single immunization of the adenovirus vector–based vaccine Ad26.COV2.S or sham and then challenged them with 5 × 10 5 median tissue culture infectious dose SARS-CoV-2 B.1.617.2 (Delta) by the intranasal and intratracheal routes. All vaccinated animals were infected by this high-dose challenge but showed rapid virologic control in nasal swabs and bronchoalveolar lavage by day 4 after challenge. However, administration of an anti-CD8α– or anti-CD8β–depleting monoclonal antibody in vaccinated animals before SARS-CoV-2 challenge resulted in higher levels of peak and day 4 virus in both the upper and lower respiratory tracts. These data demonstrate that CD8 + T cells contribute substantially to vaccine protection against SARS-CoV-2 replication in macaques.
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CD8+ T cells contribute to virological control of SARS-CoV-2 infection when antibody titres are sub-optimal in non-human primates.
“CD8+ T cells have been shown to contribute to virological control of SARS-CoV-2 infection when antibodies titres were sub-optimal in non-human primates33,34.”
From Efficacy of an unmodified bivalent mRNA vaccine against SARS-CoV-2 variants in female small animal models (2023) · cites this paper as [34]
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LSDV-Vectored SARS-CoV-2 S and N Vaccine Protects against Severe Clinical Disease in Hamsters
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- Authors
- Liu, J., Yu, J., McMahan, K., Jacob-Dolan, C., He, X., Giffin, V., Wu, C., Sciacca, M., Powers, O., Nampanya, F., Miller, J., Lifton, M., Hope, D., Hall, K., Hachmann, N. P., Chung, B., Anioke, T., Li, W., Muench, J., Gamblin, A., Boursiquot, M., Cook, A., Lewis, M. G., Andersen, H., & Barouch, D. H.
- Affiliations
- Beth Israel Deaconess Medical Center (US)
- University of Massachusetts Lowell (US)
- Bioqual (US)
- Bioqual, Rockville, MD 20852, USA.
- Corresponding author
- Liu, Jinyan
- Yu, Jingyou
- McMahan, Katherine
- Jacob-Dolan, Catherine
- He, Xuan
- Giffin, Victoria
- Barouch, Dan H.
- ORCID
- Liu, Jinyan
- Yu, Jingyou
- McMahan, Katherine
- Jacob-Dolan, Catherine
- He, Xuan
- Giffin, Victoria
- Wu, Cindy
- Powers, Olivia
- Nampanya, Felix
- Miller, Jessica
- Lifton, Michelle
- Hope, David
- Hachmann, Nicole P.
- Chung, Benjamin
- Anioke, Tochi
- Li, Wenjun
- Muench, Jeanne
- Gamblin, Adrienne
- Boursiquot, Mona
- Cook, Anthony
- Lewis, Mark G.
- Andersen, Hanne
- Barouch, Dan H.
- Venue
- Science Immunology
- Published
- 2022-11-25
- Volume
- 7
- Issue
- 77
- Pages
- eabq7647-eabq7647
- ISSN
- 2470-9468 (ISSN-L)
- PMC
- PMC9407944
- OpenAlex
- W4290774080
- Cited by
- 132
- References
- 31
- Citations by year
- 2026: 6 · 2025: 28 · 2024: 36 · 2023: 50 · 2022: 11 · 2021: 1
- FWCI
- 15.28
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Science Immunology (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (#75N93021C00014)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Life Sciences › Immunology and Microbiology › Virology › HIV Research and Treatment
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Keywords
- CD8+ T cells, SARS-CoV-2, adenovirus vector vaccine, Ad26.COV2-S, rhesus monkeys, Delta variant, viral load control, respiratory infections
- MeSH terms
- COVID-19, SARS-CoV-2, Ad26COVS1, Animals, Humans, Macaca mulatta, Viral Vaccines, CD8-Positive T-Lymphocytes
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