| Literature DB >> 28286199 |
Yang Song1, Min-Min Shi1, Yuan-Yuan Zhang2, Xiao-Dong Mo2, Yu Wang2, Xiao-Hui Zhang2, Lan-Ping Xu2, Xiao-Jun Huang1, Yuan Kong3.
Abstract
Prolonged isolated thrombocytopenia (PT) is a serious complication after allogeneic hematopoietic stem cell transplantation (allo-HSCT). Whether abnormalities of the bone marrow (BM) immune microenvironment are involved in the pathogenesis of PT remains unknown, however. Twenty patients with PT, 40 matched patients with good graft function (GGF) after allo-HSCT, and 20 healthy donors (HD) were enrolled in this nested case-control study. Th1, Th2, Tc1, Tc2, Th17, and Treg cells were analyzed by flow cytometry, and IFN-γ, IL-4, IL-17, IL-6, IL-21, and thrombopoietin levels in BM plasma were evaluated with a cytometric bead assay and ELISA. Relative to GGF patients and HD controls, PT patients had significantly higher proportions of Th1 and Tc1 cells, resulting in higher Th1/Th2 and Tc1/Tc2 ratios in the BM microenvironment. In addition, the excessive polarization of Th17 was observed in patients with PT. Changes in BM plasma cytokines were consistent with our cellular findings. These results suggest that dysregulated T cell responses in the BM microenvironment might play an important role in the pathogenesis of PT.Entities:
Keywords: Allogeneic hematopoietic stem cell transplantation; Bone marrow immune microenvironment; Prolonged isolated thrombocytopenia
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Year: 2017 PMID: 28286199 DOI: 10.1016/j.bbmt.2017.02.021
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742