{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,2]],"date-time":"2026-07-02T15:53:00Z","timestamp":1783007580440,"version":"3.54.5"},"reference-count":72,"publisher":"Oxford University Press (OUP)","issue":"11","license":[{"start":{"date-parts":[[2021,11,3]],"date-time":"2021-11-03T00:00:00Z","timestamp":1635897600000},"content-version":"vor","delay-in-days":473,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"funder":[{"name":"Faculty of Medicine, University of Ottawa"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2020,11,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:p>Endothelial colony-forming cells (ECFCs) hold significant promise as candidates for regenerative therapy of vascular injury. Existing studies remain largely preclinical and exhibit marked design heterogeneity. A systematic review of controlled preclinical trials of human ECFCs is needed to guide future study design and to accelerate clinical translation. A systematic search of Medline and EMBASE on 1 April 2019 returned 3131 unique entries of which 66 fulfilled the inclusion criteria. Most studies used ECFCs derived from umbilical cord or adult peripheral blood. Studies used genetically modified immunodeficient mice (n = 52) and\/or rats (n = 16). ECFC phenotypes were inconsistently characterized. While &amp;gt;90% of studies used CD31+ and CD45\u2212, CD14\u2212 was demonstrated in 73% of studies, CD146+ in 42%, and CD10+ in 35%. Most disease models invoked ischemia. Peripheral vascular ischemia (n = 29), central nervous system ischemia (n = 14), connective tissue injury (n = 10), and cardiovascular ischemia and reperfusion injury (n = 7) were studied most commonly. Studies showed predominantly positive results; only 13 studies reported \u22651 outcome with null results, three reported only null results, and one reported harm. Quality assessment with SYRCLE revealed potential sources of bias in most studies. Preclinical ECFC studies are associated with benefit across several ischemic conditions in animal models, although combining results is limited by marked heterogeneity in study design. In particular, characterization of ECFCs varied and aspects of reporting introduced risk of bias in most studies. More studies with greater focus on standardized cell characterization and consistency of the disease model are needed.<\/jats:p>\n               <jats:sec>\n                  <jats:title\/>\n               <\/jats:sec>","DOI":"10.1002\/sctm.20-0141","type":"journal-article","created":{"date-parts":[[2020,7,18]],"date-time":"2020-07-18T18:40:00Z","timestamp":1595097600000},"page":"1344-1352","source":"Crossref","is-referenced-by-count":20,"title":["Human endothelial colony-forming cells in regenerative therapy: A systematic review of controlled preclinical animal studies"],"prefix":"10.1093","volume":"9","author":[{"given":"Gary","family":"Liao","sequence":"first","affiliation":[{"name":"1 Clinical Epidemiology and Regenerative Medicine Programs Ottawa Hospital Research Institute, Ottawa, Ontario, Canada"},{"name":"2 Faculty of Medicine University of Ottawa, Ottawa, Ontario, 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