Hematopoietic stem-cell senescence and myocardial repair - Coronary artery disease genotype/phenotype analysis of post-MI myocardial regeneration response induced by CABG/CD133+ bone marrow hematopoietic stem cell treatment in RCT PERFECT Phase 3

Bone marrow stem cell clonal dysfunction by somatic mutation is suspected to affect post-infarction myocardial regeneration after coronary bypass surgery (CABG). Transcriptome and variant expression analysis was studied in the phase 3 PERFECT trial post myocardial infarction CABG and CD133+ bone mar...

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Veröffentlicht in:EBioMedicine 2020-07, Vol.57, p.102862-102862, Article 102862
Hauptverfasser: Wolfien, Markus, Klatt, Denise, Salybekov, Amankeldi A., Ii, Masaaki, Komatsu-Horii, Miki, Gaebel, Ralf, Philippou-Massier, Julia, Schrinner, Eric, Akimaru, Hiroshi, Akimaru, Erika, David, Robert, Garbade, Jens, Gummert, Jan, Haverich, Axel, Hennig, Holger, Iwasaki, Hiroto, Kaminski, Alexander, Kawamoto, Atsuhiko, Klopsch, Christian, Kowallick, Johannes T., Krebs, Stefan, Nesteruk, Julia, Reichenspurner, Hermann, Ritter, Christian, Stamm, Christof, Tani-Yokoyama, Ayumi, Blum, Helmut, Wolkenhauer, Olaf, Schambach, Axel, Asahara, Takayuki, Steinhoff, Gustav
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Sprache:eng
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Zusammenfassung:Bone marrow stem cell clonal dysfunction by somatic mutation is suspected to affect post-infarction myocardial regeneration after coronary bypass surgery (CABG). Transcriptome and variant expression analysis was studied in the phase 3 PERFECT trial post myocardial infarction CABG and CD133+ bone marrow derived hematopoetic stem cells showing difference in left ventricular ejection fraction (∆LVEF) myocardial regeneration Responders (n=14; ∆LVEF +16% day 180/0) and Non-responders (n=9; ∆LVEF -1.1% day 180/0). Subsequently, the findings have been validated in an independent patient cohort (n=14) as well as in two preclinical mouse models investigating SH2B3/LNK antisense or knockout deficient conditions. 1. Clinical: R differed from NR in a total of 161 genes in differential expression (n=23, q
ISSN:2352-3964
2352-3964
DOI:10.1016/j.ebiom.2020.102862