-
摘要: 目的: 研究慢性粒细胞白血病(CML)患者外周血中Th22细胞的比例、相关转录因子芳香烃受体(AHR)的表达水平及细胞因子IL-22的浓度,探讨Th22细胞在CML免疫机制中的作用。方法: 应用流式细胞术检测Th22细胞在33例CML患者(初诊15例,伊马替尼治疗后的CML-CP 18例)外周血中的比例,实时荧光定量PCR技术检测CML患者Th22相关转录因子AHR mRNA的表达水平,ELISA法检测细胞因子IL-22的浓度。同时以15例正常者作为对照。结果: CML初诊患者外周血的Th22细胞比例(0.43%±0.23%)明显低于伊马替尼治疗后的CML-CP患者(3.19%±1.76%,P<0.05)和对照者(2.58%±0.98%,P<0.05)。CML初诊患者外周血单个核细胞的AHR基因转录水平(0.2129±0.1746)与伊马替尼治疗后的CML-CP患者(0.8171±0.3887,P<0.05)和对照者(0.4681±0.1804,P<0.05)比较均明显降低。伊马替尼治疗后的CML-CP患者外周血AHR mRNA表达水平较对照者显著升高(P<0.05)。CML-CP患者的外周血IL-22浓度较对照者显著升高[(100.94±18.48) pg/ml:(85.14±13.46) pg/ml,P<0.05]。Th22细胞的比例与CML患者外周血白细胞计数及BCR-ABL%均呈负相关。结论: Th22细胞下调,Th22免疫功能受损可能有助于CML的发生和发展。
-
关键词:
- 白血病,粒细胞,慢性 /
- Th22细胞 /
- IL-22
Abstract: Objective: To explore the ratio of Th22 cells,the expression of transcription factors AHR and their related cytokines IL-22 in peripheral blood of chronic myeloid leukemia (CML) patients,and to further investigate the role of Th22 cells in hematological tumor immune mechanisms.Method: The proportions of Th22 cells in peripheral blood of 33 patients with CML were evaluated by flow cytometry analysis.AHR mRNA expressions were examined by RT-PCR.The levels of cytokines IL-22 were measured by ELISA.Fifteen normal subjects were used as controls.Result: The ratio of Th22 cells was significantly decreased in newly-diagnosed CML (CML-NP) patients (0.43%±0.23%) than those in chronic phase CML (CML-CP) patients (3.19%±1.76%,P<0.05) and controls (2.58%±0.98%,P<0.05).The expression of AHR was significantly decreased in CML-ND patients (0.212 9±0.174 6) compared with CML-CP patients (0.817 1±0.388 7,P<0.05) and controls (0.468 1±0.180 4,P<0.05).The mRNA level of AHR was increased in CML-CP patients than that in controls (P<0.05).The level of IL-22 in CML-CP patients was slightly higher than controls[(100.94±18.48) pg/ml vs.(85.14±13.46) pg/ml,P<0.05].There were significantly negative correlations between Th22 cells and peripheral white blood cell counts and BCR-ABL%.Conclusion: Down-regulation of Th22 cellular immunity and impaired Th22 immune function may contribute to the occurrence and development of CML.-
Key words:
- chronic myeloid leukemia /
- Th22cells /
- IL-22
-
-
[1] Duhen T,Geiger R,Jarrossay D,et al.Production of interleukin 22 but not interleukin 17 by a subset of human skin-homing memory T cells[J].Nat Immunol,2009,10:857-863.
[2] Shao LL,Zhang L,Hou Y,et al.Th22 cells as well as Th17 cells expand differentially in patients with early-stage and late-stage myelodysplastic syndrome[J].PLoS One,2012,7:e51339.
[3] Yu S,Liu C,Zhang L,et al.Elevated Th22 cells correlated with Th17 cells in peripheral blood of patients with acute myeloid leukemia[J].Int J Mol Sci,2014,15:1927-1945.
[4] Qin S,Ma S,Huang X,et al.Th22 cells are associated with hepatocellular carcinoma development and progression[J].Chin J Cancer Res,2014,26:135-141.
[5] Zhuang Y,Peng LS,Zhao YL,et al.Increased intratumoral IL-22-producing CD4(+) T cells and Th22 cells correlate with gastric cancer progression and predict poor patient survival[J].Cancer Immunol Immunother,2012,61:1965-1975.
[6] 周莉,徐运孝.调节性T细胞在慢性粒细胞白血病中的表达及临床意义[J].中国肿瘤临床,2012,39(9):502-505.
[7] Li Y,Geng S,Yin Q,et al.Decreased level of recent thymic emigrants in CD4+ and CD8+ T cells from CML patients[J].J Transl Med,2010,8:47.
[8] Trifari S,Kaplan CD,Tran EH,et al.Identification of a human helper T cell population that has abundant production of interleukin 22 and is distinct from T (H)-17,T (H)1 and T (H)2 cells[J].Nat Immunol,2009,10:864-871.
[9] Tian T,Yu S,Ma D.Th22 and related cytokines in inflammatory and autoimmune diseases[J].Expert Opin Ther Targets,2013,17:113-125.
[10] Nograles KE,Zaba LC,Shemer A,et al.IL-22-producing "T22" T cells account for upregulated IL-22 in atopic dermatitis despite reduced IL-17-producing TH17 T cells[J].J Allergy Clin Immunol,2009,123:1244-1252.
[11] Cella M,Fuchs A,Vermi W,et al.A human natural killer cell subset provides an innate source of IL-22 for mucosal immunity[J].Nature,2009,457:722-725.
-
计量
- 文章访问数: 210
- PDF下载数: 116
- 施引文献: 0