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Primary exposure to SARS-CoV-2 protects against reinfection in rhesus macaques
Open accessAbstract
Immunity from reinfection: One of the many open questions about severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection is whether an individual who has cleared the virus can be infected a second time and get sick. Chandrashekar et al. and Deng et al. generated rhesus macaque models of SARS-CoV-2 infection and tested whether natural SARS-CoV-2 infection could result in immunity to viral rechallenge. They found that animals indeed developed immune responses that protected against a second infection. Although there are differences between SARS-CoV-2 infection in macaques and in humans, these findings have key implications for public health and economic initiatives if validated in human studies. Science , this issue p. 812 , p. 818
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“Initial studies in macaques showed that a primary infection with SARS-CoV-2 protects against subsequent viral challenge for at least 28–35 days, with re-exposure driving memory immune responses that included boosting of binding and neutralizing antibody levels as well as of IFNγ secretion by T cells46,47.”
From Prospects for durable immune control of SARS-CoV-2 and prevention of reinfection (2021) · cites this paper as [46]
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“Preexisting immunity to SARS-CoV-2 is associated with protection against reinfection in humans (9–11) and in nonhuman primates (12, 13).”
From mRNA vaccination boosts cross-variant neutralizing antibodies elicited by SARS-CoV-2 infection (2021) · cites this paper as [13]
In the citing paper
“Animals infected with SARS-CoV-2 were protected from a high dose re-challenge with SARS-CoV-2 1 month later, and protection was associated with neutralizing antibodies”
From Adaptive immunity to SARS-CoV-2 and COVID-19 (2021) · cites this paper as Deng et al., 2020
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Self-citationThe pathogenicity of SARS-CoV-2 in hACE2 transgenic mice
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Self-citationRespiratory disease in rhesus macaques inoculated with SARS-CoV-2
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Clinical benefit of remdesivir in rhesus macaques infected with SARS-CoV-2
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Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection.
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Metadata
- Authors
- Deng, W., Bao, L., Liu, J., Xiao, C., Liu, J., Xue, J., Lv, Q., Qi, F., Gao, H., Yu, P., Xu, Y., Qu, Y., Li, F., Xiang, Z., Yu, H., Gong, S., Liu, M., Wang, G., Wang, S., Song, Z., Liu, Y., Zhao, W., Han, Y., Zhao, L., Liu, X., Wei, Q., & Qin, C.
- Affiliations
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Capital Medical University (CN)
- Beijing Key Laboratory for Animal Models of Emerging and Remerging Infectious Diseases, NHC Key Laboratory of Human Disease Comparative Medicine, Institute of Laboratory Animal Science, Chinese Academy of Medical Sciences and Comparative Medicine Center, Peking Union Medical College, Beijing, China.
- Corresponding author
- Deng, Wei
- Bao, Linlin
- Liu, Jiangning
- Xiao, Chong
- Liu, Jiayi
- Xue, Jing
- Lv, Qi
- Qin, Chuan
- ORCID
- Venue
- Science
- Published
- 2020-08-14
- Volume
- 369
- Issue
- 6505
- Pages
- 818-823
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC7402625
- OpenAlex
- W3038698073
- Cited by
- 440
- References
- 16
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 18 · 2023: 41 · 2022: 84 · 2021: 176 · 2020: 104
- FWCI
- 13.33
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Science (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Funders
- National key research and development project of China (2016YFD0500304)
- National Mega projects of China for Major Infectious Diseases (2017ZX10304402)
- CAMS Initiative for Innovative Medicine of China (2016-I2M-2-006)
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Life Sciences › Agricultural and Biological Sciences › Animal Science and Zoology › Animal Virus Infections Studies
- Health Sciences › Medicine › Infectious Diseases › COVID-19 Clinical Research Studies
- Keywords
- SARS-CoV-2, COVID-19 pandemic, reinfection, rhesus monkeys, primary infection, drug rechallenge, neutralizing antibodies, humoral immunity, cell-mediated immunity, interstitial lung disease, viral dissemination, convalescence
- MeSH terms
- Betacoronavirus, Host Microbial Interactions, COVID-19, SARS-CoV-2, Animals, Antibodies, Viral, Anal Canal, Disease Models, Animal, Immunity, Cellular, Lung, Macaca mulatta, Nasopharynx, Pneumonia, Viral, Recurrence, Virus Replication, B-Lymphocyte Subsets, T-Lymphocyte Subsets, Lung Diseases, Interstitial, Coronavirus Infections, Viral Load, Immunity, Humoral, Antibodies, Neutralizing, Pandemics
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