Optimization of the engineered 3D hepatic microenvironment enhances pluripotent stem cell derived hepatocyte
- Funded by National Institutes of Health (NIH)
- Total publications:0 publications
Grant number: 3R01DK121072-01A1S1
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Key facts
Disease
COVID-19Start & end year
20202022Known Financial Commitments (USD)
$381,375Funder
National Institutes of Health (NIH)Principal Investigator
Robert E SchwartzResearch Location
United States of AmericaLead Research Institution
Weill Cornell Medicine - Cornell UniversityResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Disease pathogenesis
Special Interest Tags
N/A
Study Type
Non-Clinical
Clinical Trial Details
N/A
Broad Policy Alignment
Pending
Age Group
Not Applicable
Vulnerable Population
Not applicable
Occupations of Interest
Not applicable
Abstract
Project summaryIn late 2019, COVID-19, a disease caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged in Wuhan, China and has rapidly impacted almost all countries around the world. Officiallydeclared a global pandemic by the WHO, COVID-19 is a worldwide emergency and bymillion United with directly , current in vitro model platforms are so distinct from human infection that they may not capture key components of viral infection or virus-host interactions. May 29, 2020, over 5.8 COVID-19 cases were reported with over 360,000 deaths globally. Although originating in China the States has emerged as an epicenter of this pandemic with over 1.75 million COVID-19 cases reportedover 103,000 deaths. Unfortunately there is no vaccine that can prevent SARS-CoV-2 infection or robustactiving antivirals that can mitigate infection or alter disease progression. MoreoverGiven this local, national, and global emergency our near-term goal is on the development of novel and robustexperimental cell culture models, virological tools, and to identify novel therapeutics for SARS-CoV-2 treatment.Our long-term goal is to elucidate the complex interactions and mechanisms underlying SARS-CoV-2 infectionand host response. Given that our institution has been at the center of the COVID-19 pandemic here in the U.S.we have generated a wide database of clinical data that has revealed that a high prevalence of initial COVID-19 presentations are with GI manifestations with over one-half of patients noted to have biochemical evidenceof liver injury at presentation. The impact of SARS-CoV-2 infection on hepatocellular and cholangiocytefunction remains unclear. To address these knowledge gaps we have generated several novel technologiesand have assembled a robust team with complimentary expertise in stem cell biology, tissue engineering andvirology, chemical screening and stem cell biology, and in virology/BSL3 expertise. We aim to identify drugcandidates that impact SARS-CoV-2 viral infection while we evaluate host-virus interactions.Our work is urgently needed given the impacts SARS-CoV-2 has had on our local, national, and globalcommunities and its potential impact on millions of people who already, or will in the future will developCOVID19 infection by shedding light on mechanisms, molecular targets, and potential drugs that could leaddirectly to the development of new antiviral treatments and therapies.