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-19
  • Start & end year

    2020
    2022
  • Known Financial Commitments (USD)

    $381,375
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    Robert E Schwartz
  • Research Location

    United States of America
  • Lead Research Institution

    Weill Cornell Medicine - Cornell University
  • Research 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.