Literature DB >> 17882720

Number of megakaryocytic progenitors and adhesion molecule expression of stem cells predict platelet engraftment after allogeneic hematopoietic stem cell transplantation.

K S Woo1, R Y Goh, S H Kim, H C Kwon, H J Kim, Y H Lee, J Y Han.   

Abstract

BACKGROUND: The mechanism of platelet recovery after hematopoietic stem cell transplantation and the factors that influence its time-course are not fully understood. Rapid hematopoietic recovery results in a reduction of transplantation-related complications. In the present study, we questioned and analyzed whether there were important factors predicting the speed of platelet engraftment.
METHODS: Thirty-seven patients with various hematologic diseases transplanted with allogeneic BM between January 2002 and December 2005 were included. We investigated the differences in mononuclear cell counts (MNC), numbers of infused CD34(+), CD34(+) CD41(+) and CD34(+) CD61(+) cells and phenotypic analysis of homing-associated cell adhesion molecules (CXCR4, CD49d and CD49e). The number of megakaryocytes formed in vitro (colony-forming unit-megakaryocytes; CFU-Mk) was also measured.
RESULTS: Median days of ANC >/=0.5x10(9)/L and platelet count >/=20x10(9)/L were 14.8 and 17.3, respectively. The number of infused CD34(+) CD41(+) and CD34(+) CD61(+) cells correlated much better with the time to platelet engraftment than that of infused CD34(+)cells (P<0.05 each). Rapid platelet recovery also occurred in patients receiving both higher homing-associated cell adhesion molecule doses and CFU-Mk (P<0.05 each). DISCUSSION: Rapid platelet recovery has several advantages, including reducing the cost of supportive therapy and reducing the risk of fatal bleeding as a result of severe thrombocytopenia. Our findings suggest that phenotypic and clonogenic assessment of infused progenitor cells can identify patients in whom platelet engraftment is likely to be significantly delayed, and new strategies to overcome related problems might be employed in the very near future.

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Year:  2007        PMID: 17882720     DOI: 10.1080/14653240701561337

Source DB:  PubMed          Journal:  Cytotherapy        ISSN: 1465-3249            Impact factor:   5.414


  4 in total

1.  A hyperactive Mpl-based cell growth switch drives macrophage-associated erythropoiesis through an erythroid-megakaryocytic precursor.

Authors:  Eyayu Belay; Chris P Miller; Amanda N Kortum; Beverly Torok-Storb; C Anthony Blau; David W Emery
Journal:  Blood       Date:  2014-10-24       Impact factor: 22.113

2.  Eltrombopag post autologous hematopoietic stem cell transplant - an emerging indication in younger pediatric patients.

Authors:  Aditya Kumar Gupta; Prasanth Srinivasan; Gargi Das; Jagdish Prasad Meena; Pranay Tanwar; Rachna Seth
Journal:  Am J Blood Res       Date:  2021-04-15

3.  Human NOTCH4 is a key target of RUNX1 in megakaryocytic differentiation.

Authors:  Yueying Li; Chen Jin; Hao Bai; Yongxing Gao; Shu Sun; Lei Chen; Lei Qin; Paul P Liu; Linzhao Cheng; Qian-Fei Wang
Journal:  Blood       Date:  2017-11-03       Impact factor: 22.113

4.  Safety and Efficacy of Megakaryocytes Induced from Hematopoietic Stem Cells in Murine and Nonhuman Primate Models.

Authors:  Xin Guan; Meng Qin; Yu Zhang; Yanan Wang; Bin Shen; Zhihua Ren; Xinxin Ding; Wei Dai; Yongping Jiang
Journal:  Stem Cells Transl Med       Date:  2016-10-07       Impact factor: 6.940

  4 in total

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