Elevated Th22 cells correlated with Th17 cells in peripheral blood of patients with acute myeloid leukemia.

Elevated Th22 cells correlated with Th17 cells in peripheral blood of patients with acute myeloid leukemia.
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急性髓系白血病患者外周血中 th22 细胞升高与 th17 细胞相关。

DOI:
10.3390/ijms15021927
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发表时间:
2014-01-27
影响因子:
5.6
通讯作者:
Ma D
Ma D
中科院分区:
生物学2区
文献类型:
--
作者:
Yu S;Liu C;Zhang L;Shan B;Tian T;Hu Y;Shao L;Sun Y;Ji C;Ma D

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Acute myeloid leukemia (AML) is a hematological tumor in which progress T helper (Th) subsets including Th22, Th17, and Th1 cells play a pivotal role. However, the role of T helper (Th) subsets in the immune pathogenesis of AML remains unclear. Here, we investigated frequencies of Th22, Th17, pure Th17, and Th1 cells in the peripheral blood (PB) of AML patients. We demonstrated that Th22, Th17, and pure Th17 in newly-diagnosed (ND) and non-complete remission (Non-CR) AML patients and plasma IL-22 in ND AML patients were significantly increased. Retinoid-related orphan receptor C (RORC) expression was significantly elevated in CR and Non-CR AML patients. However, Th1 in ND AML patients and IL-17 in ND, Non-CR or CR AML patients was significantly decreased compared with controls. Moreover, Th22 and IL-22 showed positive correlation with pure Th17, but Th22 showed negative correlation with Th1 in ND AML patients. RORC showed positive correlation with Th22 and approximately positive correlation with pure Th17 in Non-CR patients. PB blast cell showed positive correlation with Th22 and negative correlation with Th1 in ND AML patients. Our results indicate that Th22 and pure Th17 cells conjointly contribute to the pathogenesis of AML and might be promising novel clinical index for AML.
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