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Hematopoietic Dysfunction during Graft-Versus-Host Disease: A Self-Destructive Process?
被引:14
作者:

Muskens, Konradin F.
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机构:
Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands

Lindemans, Caroline A.
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机构:
Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands
Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, NL-3584 EA Utrecht, Netherlands Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands

Belderbos, Mirjam E.
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h-index: 0
机构:
Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands
机构:
[1] Princess Maxima Ctr Pediat Oncol, NL-3584 CS Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Wilhelmina Childrens Hosp, NL-3584 EA Utrecht, Netherlands
来源:
基金:
荷兰研究理事会;
关键词:
hematopoietic stem cell transplantation;
graft-versus-host disease;
hematopoiesis;
bone marrow niche;
cytopenia;
poor graft function;
graft failure;
NECROSIS-FACTOR-ALPHA;
BONE-MARROW-TRANSPLANTATION;
STEM-CELL TRANSPLANTATION;
DONOR T-CELLS;
INTERFERON-GAMMA;
PROGENITOR CELLS;
FAS-LIGAND;
ACUTE GVHD;
FUNCTIONAL EXPRESSION;
REGULATES MAINTENANCE;
D O I:
10.3390/cells10082051
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
Graft-versus-host disease (GvHD) is a major complication of allogeneic hematopoietic (stem) cell transplantation (HCT). Clinically, GvHD is associated with severe and long-lasting hematopoietic dysfunction, which may contribute to the high mortality of GvHD after HCT. During GvHD, excessive immune activation damages both hematopoietic stem and progenitor cells and their surrounding bone marrow niche, leading to a reduction in cell number and functionality of both compartments. Hematopoietic dysfunction can be further aggravated by the occurrence-and treatment-of HCT-associated complications. These include immune suppressive therapy, coinciding infections and their treatment, and changes in the microbiome. In this review, we provide a structured overview of GvHD-mediated hematopoietic dysfunction, including the targets in the bone marrow, the mechanisms of action and the effect of GvHD-related complications and their treatment. This information may aid in the identification of treatment options to improve hematopoietic function in patients, during and after GvHD.
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