Lack of Reinfection in Rhesus Macaques Infected with SARS-CoV-2
Open accessAbstract
A global pandemic of Corona Virus Disease 2019 (COVID-19) caused by severe acute respiratory syndrome CoV-2 (SARS-CoV-2) is ongoing spread. It remains unclear whether the convalescing patients have a risk of reinfection. Rhesus macaques were rechallenged with SARS-CoV-2 during an early recovery phase from initial infection characterized by weight loss, interstitial pneumonia and systemic viral dissemination mainly in respiratory and gastrointestinal tracts. The monkeys rechallenged with the identical SARS-CoV-2 strain have failed to produce detectable viral dissemination, clinical manifestations and histopathological changes. A notably enhanced neutralizing antibody response might contribute the protection of rhesus macaques from the reinfection by SARS-CoV-2. Our results indicated that primary SARS-CoV-2 infection protects from subsequent reinfection. One Sentence Summary: Neutralizing antibodies against SARS-CoV-2 might protect rhesus macaques which have undergone an initial infection from reinfection during early recovery days.
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In rhesus macaques, IC50 titers as low as 1:8 were associated with protection from re-infection, and IC50 titers as low as 1:50 were associated with reduced viral load and protection from lung pathology.
“In the former report, IC50 titers as low as 1:8 were associated with protection from re-infection while in the latter, IC50 titers as low as 1:50 were associated with reduced viral load and protection from lung pathology.”
From An <i>Alphavirus</i> -derived replicon RNA vaccine induces SARS-CoV-2 neutralizing antibody and T cell responses in mice and nonhuman primates (2020) · cites this paper as [51]
The ‘former report’ is this paper; the ‘latter’ finding is attributed to a different report and is not assessed here. In ‘SARS-CoV-2-infection protect monkeys from reinfection’ (page unavailable), the paper reports no detectable viral load after rechallenge and suggests neutralizing antibodies might protect against reinfection. Our copy does not establish the specific IC50 titer of 1:8; the Table 1 text is garbled. (LLM, conf=0.82)
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- Authors
- Bao, L., Deng, W., Gao, H., Xiao, C., Liu, J., Xue, J., Lv, Q., Liu, J., Yu, P., Xu, Y., Qi, F., 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)
- Corresponding author
- Qin, Chuan
- ORCID
- Venue
- bioRxiv (Cold Spring Harbor Laboratory)
- Publisher
- openRxiv
- Published
- 2020-03-14
- OpenAlex
- W3100347672
- Cited by
- 419
- References
- 1
- Citations by year
- 2024: 3 · 2023: 12 · 2022: 21 · 2021: 92 · 2020: 291
- Type
- posted content
- Language
- en
- Open access
- green
- doi.org
- Locations
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- Funders
- Chinese Academy of Medical Sciences Initiative for Innovative Medicine
- 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, neutralizing antibodies, convalescence, drug rechallenge, humoral immunity, viral dissemination, interstitial lung disease
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