AI Article Synopsis

  • A novel coronavirus, SARS-CoV-2, is responsible for the COVID-19 pandemic, and animal models, especially non-human primates, are crucial for studying disease mechanisms and testing vaccines.
  • Research shows that SARS-CoV-2 infects both rhesus and cynomolgus macaques, causing lung damage similar to mild human cases, with comparable immune responses in both species.
  • A new lung histopathology scoring method has been developed to enhance study decisions, suggesting both macaque species should be used for safe and effective intervention evaluations, helping to reduce reliance on rhesus macaques.

Article Abstract

A novel coronavirus, SARS-CoV-2, has been identified as the causative agent of the current COVID-19 pandemic. Animal models, and in particular non-human primates, are essential to understand the pathogenesis of emerging diseases and to assess the safety and efficacy of novel vaccines and therapeutics. Here, we show that SARS-CoV-2 replicates in the upper and lower respiratory tract and causes pulmonary lesions in both rhesus and cynomolgus macaques. Immune responses against SARS-CoV-2 are also similar in both species and equivalent to those reported in milder infections and convalescent human patients. This finding is reiterated by our transcriptional analysis of respiratory samples revealing the global response to infection. We describe a new method for lung histopathology scoring that will provide a metric to enable clearer decision making for this key endpoint. In contrast to prior publications, in which rhesus are accepted to be the preferred study species, we provide convincing evidence that both macaque species authentically represent mild to moderate forms of COVID-19 observed in the majority of the human population and both species should be used to evaluate the safety and efficacy of interventions against SARS-CoV-2. Importantly, accessing cynomolgus macaques will greatly alleviate the pressures on current rhesus stocks.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7904795PMC
http://dx.doi.org/10.1038/s41467-021-21389-9DOI Listing

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