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Exploring disease-causing traits for drug repurposing in critically ill COVID-19 patients: A causal inference approach.
Baukmann, Hannes A; Cope, Justin L; Bannard, Colin; Schwinges, Alexander R E C; Lamparter, Margaretha R J; Groves, Sarah; Ravarani, Charles N J; Amulic, Borko; Klinger, Joern E; Schmidt, Marco F.
Affiliation
  • Baukmann HA; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Cope JL; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Bannard C; University of Manchester, Oxford Road, Manchester M13 9PL, UK.
  • Schwinges AREC; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Lamparter MRJ; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Groves S; School of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol BS8 1DT, UK.
  • Ravarani CNJ; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Amulic B; School of Cellular and Molecular Medicine, Faculty of Life Sciences, University of Bristol, Bristol BS8 1DT, UK.
  • Klinger JE; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
  • Schmidt MF; biotx.ai GmbH, Am Mühlenberg 11, 14476 Potsdam, Germany.
iScience ; 26(11): 108185, 2023 Nov 17.
Article in En | MEDLINE | ID: mdl-37965141
ABSTRACT
Despite recent development of vaccines to prevent SARS-CoV-2 infection, treatment of critically ill COVID-19 patients remains an important goal. In principle, genome-wide association studies (GWASs) provide a shortcut to the clinical evidence needed to repurpose existing drugs; however, genes identified frequently lack a causal disease link. We report an alternative method for finding drug repurposing targets, focusing on disease-causing traits beyond immediate disease genetics. Sixty blood cell types and biochemistries, and body mass index, were screened on a cohort of critically ill COVID-19 cases and controls that exhibited mild symptoms after infection, yielding high neutrophil cell count as a possible causal trait for critical illness. Our methodology identified CDK6 and janus kinase (JAK) inhibitors as treatment targets that were validated in an ex vivo neutrophil extracellular trap (NET) formation assay. Our methodology demonstrates the increased power for drug target identification by leveraging large disease-causing trait datasets.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2023 Document type: Article Affiliation country: Germany