TY - JOUR
T1 - Not all stem cells are created equal the case for prospective assessment of stem cell potency in the cardiamp heart failure trial
AU - Johnston, Peter V.
AU - Duckers, Henricus J.
AU - Raval, Amish N.
AU - Cook, Thomas D.
AU - Pepine, Carl J.
N1 - Funding Information:
CardiAMP-HF is funded by BioCardia, Inc, San Carlos, CA, and by the Maryland Stem Cell Research Fund (2016-MSCRFP-2804). C.J. Pepine receives funding from the Cardiovascular Cell Therapy Research Network NIH/NHLBI UM1 HL087366.
Funding Information:
CardiAMP-HF is funded by BioCardia, Inc, San Carlos, CA, and by the Maryland Stem Cell Research Fund (2016-MSCRFP-2804).
Funding Information:
C.J. Pepine receives funding from the Cardiovascular Cell Therapy Research Network NIH/NHLBI UM1 HL087366.
Publisher Copyright:
© 2018 American Heart Association, Inc.
PY - 2018
Y1 - 2018
N2 - Stem ure (CHF) cell therapy management holds promise as animal for chronic studies heart document fail-that these cells modify local inflammatory conditions, release factors that stimulate angiogenesis and intrinsic tissue repair, modify adverse ventricular remodeling, and restore function.1 Clinical trial results, however, are more variable with some showing beneficial effects and others without.2,3 Preclinical studies are conducted in otherwise healthy animals, but clinical studies enroll CHF patients with multiple comorbidities (aging, diabetes mellitus, hypertension, inflammation, etc) that negatively affect regenerative capacity.4 Significant variability in regenerative response is linked with variations in cell characteristics (eg, migratory and adhesion capacity, clonogenicity, surface marker expression, and paracrine factor release).5,6 Using a personalized medicine approach (ie, tailoring treatment to patient characteristics to optimize benefit), we propose to optimize cardiac cell therapy efficacy by prospectively selecting patients most likely to benefit using a cell potency assay to assess inherent regenerative capacity.
AB - Stem ure (CHF) cell therapy management holds promise as animal for chronic studies heart document fail-that these cells modify local inflammatory conditions, release factors that stimulate angiogenesis and intrinsic tissue repair, modify adverse ventricular remodeling, and restore function.1 Clinical trial results, however, are more variable with some showing beneficial effects and others without.2,3 Preclinical studies are conducted in otherwise healthy animals, but clinical studies enroll CHF patients with multiple comorbidities (aging, diabetes mellitus, hypertension, inflammation, etc) that negatively affect regenerative capacity.4 Significant variability in regenerative response is linked with variations in cell characteristics (eg, migratory and adhesion capacity, clonogenicity, surface marker expression, and paracrine factor release).5,6 Using a personalized medicine approach (ie, tailoring treatment to patient characteristics to optimize benefit), we propose to optimize cardiac cell therapy efficacy by prospectively selecting patients most likely to benefit using a cell potency assay to assess inherent regenerative capacity.
KW - Bone marrow cells
KW - Clinical trial
KW - Heart failure
KW - Regeneration
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=85055600929&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85055600929&partnerID=8YFLogxK
U2 - 10.1161/CIRCRESAHA.118.313425
DO - 10.1161/CIRCRESAHA.118.313425
M3 - Review article
C2 - 30355037
AN - SCOPUS:85055600929
SN - 0009-7330
VL - 123
SP - 944
EP - 946
JO - Circulation Research
JF - Circulation Research
IS - 8
ER -