Bone marrow cell characteristics associated with patient profile and cardiac performance outcomes in the LateTIME-Cardiovascular Cell Therapy Research Network (CCTRN) trial

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• 作者：Aruni Bhatnagar ; PhD^a ; Roberto Bolli ; MD^a ; Brian H. Johnstone ; PhD^b ; Jay H. Traverse ; MD^c ; Timothy D. Henry ; MD^d ; Carl J. Pepine ; MD^e ; James T. Willerson ; MD^f ; Emerson C. Perin ; MD ; PhD^f ; Stephen G. Ellis ; MD^g ; David X.M. Zhao ; MD^h ; Phillip C. Yang ; MDⁱ ; John P. Cooke ; MD ; PhD^j ; Robert C. Schutt ; MD ; MS^j ; Barry H. Trachtenberg ; MD^j ; Aaron Orozco ; PhD^f ; Micheline Resende ; PhD^f ; Ray F. Ebert ; PhD^k ; Shelly L. Sayre ; MPH^l ; Robert D. Simari ; MD^m ; Lem Moyé ; MD ; PhD^l ; ^{Lemmoye@msn.com" class="auth_mail" title="E-mail the corresponding author} ; Christopher R. Cogle ; MD^e ; Doris A. Taylor ; PhD^f ; for the Cardiovascular Cell Therapy Research Network (CCTRN)
• 刊名：American Heart Journal
• 出版年：2016
• 出版时间：September 2016
• 年：2016
• 卷：179
• 期：Complete
• 页码：142-150
• 全文大小：243 K

文摘

Although several preclinical studies have shown that bone marrow cell (BMC) transplantation promotes cardiac recovery after myocardial infarction, clinical trials with unfractionated bone marrow have shown variable improvements in cardiac function.

Methods

To determine whether in a population of post–myocardial infarction patients, functional recovery after BM transplant is associated with specific BMC subpopulation, we examined the association between BMCs with left ventricular (LV) function in the LateTIME-CCTRN trial.

Results

In this population, we found that older individuals had higher numbers of BM CD133⁺ and CD3⁺ cells. Bone marrow from individuals with high body mass index had lower CD45^dim/CD11b^dim levels, whereas those with hypertension and higher C-reactive protein levels had higher numbers of CD133⁺ cells. Smoking was associated with higher levels of CD133⁺/CD34⁺/VEGFR2⁺ cells and lower levels of CD3⁺ cells. Adjusted multivariate analysis indicated that CD11b^dim cells were negatively associated with changes in LV ejection fraction and wall motion in both the infarct and border zones. Change in LV ejection fraction was positively associated with CD133⁺, CD34⁺, and CD45⁺/CXCR4^dim cells as well as faster BMC growth rates in endothelial colony forming assays.

Conclusions

In the LateTIME population, BM composition varied with patient characteristics and treatment. Irrespective of cell therapy, recovery of LV function was greater in patients with greater BM abundance of CD133⁺ and CD34⁺ cells and worse in those with higher levels of CD11b^dim cells. Bone marrow phenotype might predict clinical response before BMC therapy and administration of selected BM constituents could potentially improve outcomes of other future clinical trials.