Evaluating mesenchymal stem cell therapy for sepsis with preclinical meta-analyses prior to initiating a first-in-human trial

Author:

Lalu Manoj M123ORCID,Sullivan Katrina J2,Mei Shirley HJ3,Moher David24,Straus Alexander2,Fergusson Dean A2,Stewart Duncan J35ORCID,Jazi Mazen26,MacLeod Malcolm7,Winston Brent8,Marshall John9,Hutton Brian2,Walley Keith R10,McIntyre Lauralyn211ORCID,

Affiliation:

1. Department of Anesthesiology and Pain Medicine, The Ottawa Hospital, Ottawa, Canada

2. Clinical Epidemiology Program, The Ottawa Hospital Research Institute, Ottawa, Canada

3. Regenerative Medicine Program, The Ottawa Hospital Research Institute, Ottawa, Canada

4. School of Epidemiology, Public Health and Preventive Medicine, University of Ottawa, Ottawa, Canada

5. Department of Cell and Molecular Medicine, University of Ottawa, Ottawa, Canada

6. Faculty of Medicine, University of Ottawa, Ottawa, Canada

7. Centre for Clinical Brain Sciences, The University of Edinburgh, Edinburgh, United Kingdom

8. Department of Critical Care Medicine, University of Calgary, Calgary, Canada

9. Departments of Surgery and Critical Care Medicine, Keenan Research Centre of the Li KaShing Knowledge Institute, St. Michaels Hospital, The University of Toronto, Toronto, Canada

10. Department of Medicine, Centre for Heart Lung Innovation, University of British Columbia, Vancouver, Canada

11. Department of Medicine, University of Ottawa, Ottawa, Canada

Abstract

Evaluation of preclinical evidence prior to initiating early-phase clinical studies has typically been performed by selecting individual studies in a non-systematic process that may introduce bias. Thus, in preparation for a first-in-human trial of mesenchymal stromal cells (MSCs) for septic shock, we applied systematic review methodology to evaluate all published preclinical evidence. We identified 20 controlled comparison experiments (980 animals from 18 publications) of in vivo sepsis models. Meta-analysis demonstrated that MSC treatment of preclinical sepsis significantly reduced mortality over a range of experimental conditions (odds ratio 0.27, 95% confidence interval 0.18–0.40, latest timepoint reported for each study). Risk of bias was unclear as few studies described elements such as randomization and no studies included an appropriately calculated sample size. Moreover, the presence of publication bias resulted in a ~30% overestimate of effect and threats to validity limit the strength of our conclusions. This novel prospective application of systematic review methodology serves as a template to evaluate preclinical evidence prior to initiating first-in-human clinical studies.

Funder

Heart and Stroke Foundation of Canada

University of Ottawa

National Centre for the Replacement, Refinement and Reduction of Animals in Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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