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

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...

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Autores principales: Abdulla, Aynur, Wang, Boqian, Qian, Feng, Kee, Theodore, Blasiak, Agata, Ong, Yoong Hun, Hooi, Lissa, Parekh, Falgunee, Soriano, Rafael, Olinger, Gene G., Keppo, Jussi, Hardesty, Chris L., Chow, Edward K., Ho, Dean, Ding, Xianting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235487/
https://www.ncbi.nlm.nih.gov/pubmed/32838027
http://dx.doi.org/10.1002/adtp.202000034
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author Abdulla, Aynur
Wang, Boqian
Qian, Feng
Kee, Theodore
Blasiak, Agata
Ong, Yoong Hun
Hooi, Lissa
Parekh, Falgunee
Soriano, Rafael
Olinger, Gene G.
Keppo, Jussi
Hardesty, Chris L.
Chow, Edward K.
Ho, Dean
Ding, Xianting
author_facet Abdulla, Aynur
Wang, Boqian
Qian, Feng
Kee, Theodore
Blasiak, Agata
Ong, Yoong Hun
Hooi, Lissa
Parekh, Falgunee
Soriano, Rafael
Olinger, Gene G.
Keppo, Jussi
Hardesty, Chris L.
Chow, Edward K.
Ho, Dean
Ding, Xianting
author_sort Abdulla, Aynur
collection PubMed
description 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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spelling pubmed-72354872020-05-19 Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention Abdulla, Aynur Wang, Boqian Qian, Feng Kee, Theodore Blasiak, Agata Ong, Yoong Hun Hooi, Lissa Parekh, Falgunee Soriano, Rafael Olinger, Gene G. Keppo, Jussi Hardesty, Chris L. Chow, Edward K. Ho, Dean Ding, Xianting Adv Ther (Weinh) Full Papers 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. John Wiley and Sons Inc. 2020-04-16 2020-07 /pmc/articles/PMC7235487/ /pubmed/32838027 http://dx.doi.org/10.1002/adtp.202000034 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Full Papers
Abdulla, Aynur
Wang, Boqian
Qian, Feng
Kee, Theodore
Blasiak, Agata
Ong, Yoong Hun
Hooi, Lissa
Parekh, Falgunee
Soriano, Rafael
Olinger, Gene G.
Keppo, Jussi
Hardesty, Chris L.
Chow, Edward K.
Ho, Dean
Ding, Xianting
Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title_full Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title_fullStr Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title_full_unstemmed Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title_short Project IDentif.AI: Harnessing Artificial Intelligence to Rapidly Optimize Combination Therapy Development for Infectious Disease Intervention
title_sort project identif.ai: harnessing artificial intelligence to rapidly optimize combination therapy development for infectious disease intervention
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7235487/
https://www.ncbi.nlm.nih.gov/pubmed/32838027
http://dx.doi.org/10.1002/adtp.202000034
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