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  2. 3D-printed airway model as a platform for SARS-CoV-2 infection and antiviral drug testing

3D-printed airway model as a platform for SARS-CoV-2 infection and antiviral drug testing

  • Biomaterials. 2024 Jun 25:311:122689. doi: 10.1016/j.biomaterials.2024.122689.
Yunji Lee 1 Myoung Kyu Lee 2 Hwa-Rim Lee 1 Byungil Kim 2 Meehyein Kim 3 Sungjune Jung 4
Affiliations

Affiliations

  • 1 Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.
  • 2 Infectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, 34114, Republic of Korea.
  • 3 Infectious Diseases Therapeutic Research Center, Korea Research Institute of Chemical Technology (KRICT), Daejeon, 34114, Republic of Korea; Graduate School of New Drug Discovery and Development, Chungnam National University, Daejeon, 34134, Republic of Korea. Electronic address: mkim@krict.re.kr.
  • 4 Department of Materials Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea; Institute for Convergence Research and Education in Advanced Technology, Yonsei University, Seoul, 03722, Republic of Korea. Electronic address: sjjung@postech.ac.kr.
Abstract

We present a bioprinted three-layered airway model with a physiologically relevant microstructure for the study of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Infection dynamics. This model exhibited clear cell-cell junctions and mucus secretion with an efficient expression of angiotensin-converting Enzyme 2 (ACE2) and transmembrane serine Protease 2 (TMPRSS2). Having infected air-exposed epithelial cells in the upper layer with a minimum multiplicity of Infection of 0.01, the airway model showed a marked susceptibility to SARS-CoV-2 within one-day post-infection (dpi). Furthermore, the unique longevity allowed the observation of cytopathic effects and barrier degradation for 21 dpi. The in-depth transcriptomic analysis revealed dramatic changes in gene expression affecting the Infection pathway, viral proliferation, and host immune response which are consistent with COVID-19 patient data. Finally, the treatment of Antiviral agents, such as remdesivir and molnupiravir, through the culture medium underlying the endothelium resulted in a marked inhibition of viral replication within the epithelium. The bioprinted airway model can be used as a manufacturable physiological platform to study disease pathogeneses and drug efficacy.

Keywords

3D airway model; Antiviral therapeutics; Inkjet bioprinting; SARS-CoV-2.

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