4.4 Article

Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention

Journal

ADVANCED THERAPEUTICS
Volume 3, Issue 7, Pages -

Publisher

WILEY
DOI: 10.1002/adtp.202000034

Keywords

artificial intelligence; combination therapy; COVID-19; digital medicine; infectious diseases

Funding

  1. Shanghai Municipal Science and Technology [2017SHZDZX01]
  2. National Key Research and Development Program of China [2017ZX10203205-006-002]
  3. National Natural Science Foundation of China [81871448]
  4. Office of the President, Office of the Senior Deputy President and Provost, and Office of the Deputy President of Research and Technology at the National University of Singapore
  5. Ministry of Education (MOE) Tier 1 FRC grant
  6. Singapore Ministry of Health's National Medical Research Council under its Open Fund-Large Collaborative Grant (OF-LCG) [MOH-OFLCG18May-0003]

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In 2019/2020, the emergence of coronavirus disease 2019 (COVID-19) resulted in rapid increases in infection rates as well as patient mortality. Treatment options addressing COVID-19 included drug repurposing, investigational therapies such as remdesivir, and vaccine development. Combination therapy based on drug repurposing is among the most widely pursued of these efforts. Multi-drug regimens are traditionally designed by selecting drugs based on their mechanism of action. This is followed by dose-finding to achieve drug synergy. This approach is widely-used for drug development and repurposing. Realizing synergistic combinations, however, is a substantially different outcome compared to globally optimizing combination therapy, which realizes the best possible treatment outcome by a set of candidate therapies and doses toward a disease indication. To address this challenge, the results of Project IDentif.AI (Identifying Infectious Disease Combination Therapy with Artificial Intelligence) are reported. An AI-based platform is used to interrogate a massive 12 drug/dose parameter space, rapidly identifying actionable combination therapies that optimally inhibit A549 lung cell infection by vesicular stomatitis virus within three days of project start. Importantly, a sevenfold difference in efficacy is observed between the top-ranked combination being optimally and sub-optimally dosed, demonstrating the critical importance of ideal drug and dose identification. This platform is disease indication and disease mechanism-agnostic, and potentially applicable to the systematic N-of-1 and population-wide design of highly efficacious and tolerable clinical regimens. This work also discusses key factors ranging from healthcare economics to global health policy that may serve to drive the broader deployment of this platform to address COVID-19 and future pandemics.

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