Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021;6(5):374-376.
doi: 10.1038/s41578-021-00305-z. Epub 2021 Mar 17.

COVID-19 highlights the model dilemma in biomedical research

Affiliations

COVID-19 highlights the model dilemma in biomedical research

Partho Protim Adhikary et al. Nat Rev Mater. 2021.

Abstract

Scientists worldwide struggle to identify suitable animal models to study SARS-CoV-2 infections. Interspecies-related differences, such as host specificity, divergent immune responses, or the unavailability of species-specific reagents hamper the research. Human-based models, such as micro-engineered multi-organs-on-chip, may hold the solution.

Keywords: Biomaterials; Pharmacology; Preclinical research.

PubMed Disclaimer

Conflict of interest statement

Competing interestsThe authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Modular ready-to-use chips as human (patho)physiology models.
The modular chips contain complex 3D organ models, which can be interconnected in a customizable way to address specific research questions. For example, immunocompetent human lung-on-chip, brain-on-chip, liver-on-chip, intestine-on-chip and kidney-on-chip can be connected to study multi-organ-involvement in COVID-19.

References

    1. Dowden H, Munro J. Trends in clinical success rates and therapeutic focus. Nat. Rev. Drug Discov. 2019;18:495–496. doi: 10.1038/d41573-019-00074-z. - DOI - PubMed
    1. Muñoz-Fontela C, et al. Animal models for COVID-19. Nature. 2020;586:509–515. doi: 10.1038/s41586-020-2787-6. - DOI - PMC - PubMed
    1. Wei Y, Aris P, Farookhi H, Xia X. Predicting mammalian species at risk of being infected by SARS-CoV-2 from an ACE2 perspective. Sci. Rep. 2021;11:1702. doi: 10.1038/s41598-020-80573-x. - DOI - PMC - PubMed
    1. Sasaki M, et al. SARS-CoV-2 variants with mutations at the S1/S2 cleavage site are generated in vitro during propagation in TMPRSS2-deficient cells. PLoS Pathog. 2021;17:e1009233. doi: 10.1371/journal.ppat.1009233. - DOI - PMC - PubMed
    1. Han Y, et al. Identification of SARS-CoV-2 inhibitors using lung and colonic organoids. Nature. 2021;589:270–275. doi: 10.1038/s41586-020-2901-9. - DOI - PMC - PubMed

LinkOut - more resources