Human Organ-on-a-Chip Project Launched to Model Influenza Infection
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Project aims to mimic human influenza infection and pathogenesis in vitro, and identify new drug leads that target host response factors.
The Wyss Institute for Biologically Inspired Engineering has received funding from the National Institutes of Health (NIH) to leverage its human Organ-on-a-Chip (Organ Chip) microfluidic cell culture technology to develop clinically relevant in vitro models of influenza infection of human lung, and to identify new anti-viral therapeutics that act by modulating the host response to infection.
The multi-disciplinary project led by Principal Investigator (PI) and Wyss Founding Director, Donald Ingber, M.D., Ph.D., will be one of several projects within the “Tissue Chip for Disease Modeling and Efficacy Testing” initiative funded by NIH’s National Center for Advancing Translational Sciences (NCATS) in an effort to explore human microphysiological systems as potential facilitators of drug development in various disease areas. Recognizing that more than 60% of drugs fail in human clinical trials, the agency hopes to push development of better pre-clinical human models by awarding about $15 million annually to 13 two-year projects.
The development of anti-influenza drugs has been limited by the fact that animal models do not accurately reflect the infection mechanisms influenza viruses engage in humans. In the proposed studies, the Wyss Institute’s team will use lung Small Airway and Alveolus Chip devices lined by living human lung cells that they previously showed to faithfully reproduce normal lung physiology as well as lung diseases that affect these regions, including chronic obstructive pulmonary disease (COPD), asthma and pulmonary edema.
The Lung Chips are microengineered devices the size of a computer memory stick that contain two parallel hollow channels, each less than 1 millimeter wide, separated by a porous membrane. Lung alveolar cells or airway epithelial cells are cultured on the porous membrane in one channel, and lung capillary endothelial cells are grown on the opposite side of the same membrane in the second channel to recreate the characteristic tissue-tissue interface found within these lung regions. With air streaming through the lung epithelial channels and growth medium continuously streaming through the ‘vascular channels’, the team can maintain, study and manipulate the re-engineered organ units over the course of weeks to months. Deforming forces also can be applied to the tissue-tissue interface of the Alveolus Chip to mimic breathing motions of the living lung.
“Virtually all existing anti-viral drugs target the virus itself, however, the ability to study influenza infection in human Lung Chips also allows us to study the host response to infection in a highly controlled way,” said Ingber, who is also the Judah Folkman Professor of Vascular Biology at Harvard Medical School and Vascular Biology Program at Boston Children’s Hospital, as well as Professor of Bioengineering at Harvard’s John A. Paulson School of Engineering and Applied Sciences. “We hope to leverage this new capability to develop a new class of anti-influenza drugs that effectively make the lung tissues resistant to viral infection.”
By first linking the lung Airway and Alveolus Chips together, the Institute’s influenza team envisions to mimic the natural course of influenza infection, where the virus mostly infects small airway cells first and then propagates further to the lung’s alveoli to cause tissue break down, and edema. The Wyss Institute’s influenza team also will expand the lung infection model by fluidically coupling the Lung Chips to a human Liver Chip because many drugs, including the most commonly used anti-viral drugs, are known to be chemically transformed into their active metabolites in the liver.
By first linking the lung Airway and Alveolus Chips together, the Institute’s influenza team envisions to mimic the natural course of influenza infection, where the virus mostly infects small airway cells first and then propagates further to the lung’s alveoli to cause tissue break down, and edema. The Wyss Institute’s influenza team also will expand the lung infection model by fluidically coupling the Lung Chips to a human Liver Chip because many drugs, including the most commonly used anti-viral drugs, are known to be chemically transformed into their active metabolites in the liver.
To enable new drug discovery, the team will access the expertise of Co-Investigator and Wyss Institute Core Faculty member James Collins, Ph.D., a world-leading expert in synthetic biology. The team will use integrated multi-omic analysis and bioinformatics approaches to assess genome-wide changes in gene expression and alterations in the synthesis of proteins and metabolites that result from infection in the different lung Organ Chips. The analysis aims to pinpoint key changes in the host response to viral infections that may be targeted to develop new anti-influenza therapeutics. Collins is also the Termeer Professor of Medical Engineering & Science and Professor of Biological Engineering at the Massachusetts Institute of Technology’s Department of Biological Engineering.
This article has been republished from materials provided by The Wyss Institute for Biologically Inspired Engineering. Note: material may have been edited for length and content. For further information, please contact the cited source.
