Metabolomics Analysis of Mesenchymal Stem Cell (MSC) Therapy in a Phase I Clinical Trial of Septic Shock: An Exploratory Study

Author:

Banoei Mohammad1,McIntyre Lauralyn234,Stewart Duncan35,Mei Shirley36,Courtman David36,Watpool Irene3,Granton John7,Marshall John8,dos Santos Claudia8,Walley Keith9,Schlosser Kenny36,Fergusson Dean34,Winston Brent110ORCID, ,

Affiliation:

1. Department of Critical Care Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4Z6, Canada

2. Department of Medicine (Division of Critical Care), University of Ottawa, Ottawa, ON K1H 8L6, Canada

3. Ottawa Hospital Research Institute, Ottawa, ON K1H 8M5, Canada

4. Department of Epidemiology and Community Medicine, University of Ottawa, Ottawa, ON K1H 8L6, Canada

5. Department of Cell and Molecular Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada

6. Department of Regenerative Medicine, Ottawa Hospital Research Institute, Ottawa, ON K1H 8M5, Canada

7. Department of Medicine, University of Toronto, Toronto, ON M5G 2N2, Canada

8. Department of Surgery and Critical Care Medicine, Keenan Research Centre of the Li Ka Shing Knowledge Institute, St. Michael’s Hospital, The University of Toronto, Toronto, ON M5B 1W8, Canada

9. Centre for Heart Lung Innovation, University of British Columbia, Vancouver, BC V6Z 1Y6, Canada

10. Departments of Medicine and Biochemistry and Molecular Biology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4Z6, Canada

Abstract

Sepsis is the result of an uncontrolled host inflammatory response to infection that may lead to septic shock with multiorgan failure and a high mortality rate. There is an urgent need to improve early diagnosis and to find markers identifying those who will develop septic shock and certainly a need to develop targeted treatments to prevent septic shock and its high mortality. Herein, we explore metabolic alterations due to mesenchymal stromal cell (MSC) treatment of septic shock. The clinical findings for this study were already reported; MSC therapy was well-tolerated and safe in patients in this phase I clinical trial. In this exploratory metabolomics study, 9 out of 30 patients received an escalating dose of MSC treatment, while 21 patients were without MSC treatment. Serum metabolomics profiling was performed to detect and characterize metabolite changes due to MSC treatment and to help determine the sample size needed for a phase II clinical trial and to define a metabolomic response to MSC treatment. Serum metabolites were measured using 1H-NMR and HILIC-MS at times 0, 24 and 72 h after MSC infusion. The results demonstrated the significant impact of MSC treatment on serum metabolic changes in a dose- and time-dependent manner compared to non-MSC-treated septic shock patients. This study suggests that plasma metabolomics can be used to assess the response to MSC therapy and that treatment-related metabolomics effects can be used to help determine the sample size needed in a phase II trial. As this study was not powered to detect outcome, how the treatment-induced metabolomic changes described in this study of MSC-treated septic shock patients are related to outcomes of septic shock in the short and long term will need to be explored in a larger adequately powered phase II clinical trial.

Funder

Faculty of Medicine, University of Calgary, Alberta Health Services and Alberta’s Health Research Innovation Strategy

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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