Role of bone marrow T helper 17 cells in patients with immune-related pancytopenia

被引:0
|
作者
Li, Zhengfa [1 ]
Zhao, Xiaochen [2 ]
Li, Rui [1 ]
Zhang, Qin [3 ]
Jiang, Yaxian [3 ]
Hu, Peng [1 ]
Wang, Yajie [1 ]
He, Haiping [1 ]
Zhao, Renbin [1 ]
Guan, Xin [1 ]
Pei, Qiang [1 ]
Yang, Tonghua [1 ]
Feng, Jiakun [1 ]
Liu, Wei [1 ]
Gu, Shian [1 ]
Dong, Ting [3 ]
机构
[1] Kunming Univ Sci & Technol, Peoples Hosp Yunnan Prov 1, Affiliated Hosp, Dept Hematol, Kunming 650034, Yunnan, Peoples R China
[2] Yunnan Univ Tradit Chinese Med, Kunming 650500, Yunnan, Peoples R China
[3] Kunming Univ Sci & Technol, Affiliated Hosp, Dept Lab Med, Peoples Hosp Yunnan Prov 1, Kunming 650034, Yunnan, Peoples R China
关键词
Immune-Related Pancytopenia; Flow Cytometry; IL-23R(+)CD4(+)/CD4(+) Ratio; Th17; Cells; IL-6; IL-17; IL-23; TGF-BETA; ELECTROCHEMICAL BIOSENSOR; DIFFERENTIATION; PATHWAYS; T(H)17;
D O I
10.1166/mex.2021.1896
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To investigate the immunoregulatory effect of bone marrow IL-23R(+)CD4(+) T helper 17 cells and the secretion of IL-6, IL-17, and IL-23 cytokines in patients with immune-related pancytopenia (IRP). We used samples from patients with IRP, hematopoietic failure diseases (HDDs), or with complete remission after IRP immunotherapy (IRP-CR). The bone marrow IL-23R(+)CD4(+)/CD4(+) (Th17 cells) cell ratio was measured by flow cytometry (FCM). IL-6, IL-17, and IL-23 expression levels in the bone marrow supernatants were measured by enzyme-linked immunosorbent assay (ELISA). Differences among the groups were assessed. The IL-23R(+)CD4(+)/CD4(+) cell ratio and the levels of IL-6, IL-17, and IL-23 in the bone marrow supernatant of patients with IRP were significantly higher than those in the HDD, IRP-CR, and healthy groups. The IRP group was compared with the remaining three groups and differences with P < 0.05 were considered significant. No significant differences were observed among the HDD, IRP-CR, and NC groups. Taken together, we firstly observed the role of Th17 cells in the occurrence and development of IRP, which provided a new target for the therapy of IRP.
引用
收藏
页码:204 / 210
页数:7
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