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Choosing the Right Animal Model for COVID-19 Nonclinical Research
Research into drugs and vaccines to combat the ongoing COVID-19 pandemic caused by the SARS-CoV-2 virus is in full swing. How can you choose the right animal model for your nonclinical research? To begin with, defining precise and clear goals before starting a nonclinical study will help support the species selection choice. This will also ensure that the study leads to meaningful results that contribute to program success.
COVID-19 is primarily a respiratory disease, and much research has been focused on lung histopathology and on upper and lower respiratory tract viral loads. Since a virus is behind this disease, inhibiting viral replication has been another primary goal of research efforts. Given that end goals for research can vary widely and that financial and operational considerations can come into play, it is imperative that a sponsor look at the full picture before choosing an animal model.
The same factors to consider when typically looking at animal models apply here as well, along with several pandemic-specific, COVID-19-specific, and of course SARS-CoV-2-specific factors:
A variety of animal models are in use for the nonclinical study of the SARS-CoV-2 virus, each with its own advantages and disadvantages. Listed below are the most common species currently involved in these studies and some key considerations for the best use of each.
NHPs are often considered the best models to study biologics due to their similarity to humans. In this case, commonalities between the human and macaque ACE2 receptor amino acid sequence make macaques susceptible to the SARS-CoV-2 infection (which targets the ACE2 receptor).
In addition, the disease has been demonstrated to be more severe in older animals and in certain species of macaques. Recently, rhesus macaques have been used to look at immunity following disease recovery, an important avenue of research as we push forward with vaccine research. On the other hand, common marmosets have a more divergent amino acid sequence from humans and are more resistant to the virus.
A regular mouse is not a good model for COVID-19 since the ACE2 receptor is not well conserved between mice and humans. The differences in the amino acid residue sequence that make mice resistant to the virus have led researchers to use transgenic mice with the human ACE2 receptor instead.
These hACE2 (humanized ACE2 receptor) mice were originally bred for SARS research, and the sperm remained frozen at The Jackson Laboratory until they became needed again recently. Although species-specific reagents are widely available since mice are a commonly used animal model globally, high demand is limiting the availability of this transgenic strain.
While mice have a productive viral replication and visible histopathology, they exhibit minimal if any symptoms. Animals exhibiting such mild infections could be useful for testing drugs and vaccines, but scientists will need to look to other models to gain an understanding of more severe cases of the virus.
Hamsters have strong upper and lower respiratory tract viral loads, and infected models exhibit pulmonary histopathology characteristic of human COVID-19 cases. In addition, studies have shown transmission by direct contact in hamsters, but access to species-specific reagents is more limited than with mice since hamsters are not as widely used. However, hamster transgenic strains exist that could help with the study of the molecular pathways that help to restrict systemic viral dissemination.
Ferrets have a particularly robust upper respiratory tract viral burden, and infected models exhibit fever and sneezing characteristic of human COVID-19 cases. Previous research into their applicability in the study of disease transmission, by both direct and indirect contact, has recently resulted in their use in SARS-CoV-2 transmission research. Although access to species-specific reagents is also limited with ferrets, they have the advantage of size, which facilitates repeated sampling to monitor viral load, immune response, and other markers as required.
Sponsors researching the impact of COVID-19 but not attempting to inhibit viral replication should consider an additional class of animal models, for which the competition for resources is lower: surrogate animal models.
Two examples are the Lymphocytic Choriomeningitis Virus (LCV) and the Respiratory Syncytial Virus (RSV) mice and rat inflammation models. The LCV model can be used to look at the T cell-oriented immune response, while the RSV model can be used to look at lung pathology.
In short, macaques are the gold standard for testing, transgenic mice are widely used and easy to adapt, hamsters are useful to study viral replication, ferrets are good for clinical disease research, and surrogate animal models should not be forgotten.
With such an abundance of options and factors involved, the choice is not an easy or clear one. Camargo’s experts and our network of CROs involved in COVID-19 research can help you to select the right species for your nonclinical program.
Rudi Erlemann develops new business relationships for Camargo with sponsors whose research we can support. He has a background in biophysics and biochemistry and many years of experience in nonclinical program support. Connect with Rudi to learn how Camargo can help advance your product toward the clinic.
Rudi Erlemann, PhD
Vice President of Business Development and External Scientific Affairs
Camille Delouche, MSc
Commercial Operations Associate
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