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调节性T细胞在新诊断慢性髓性白血病患者中的预后价值

Prognostic value of regulatory T cells in newly diagnosed chronic myeloid leukemia patients.

作者信息

Zahran Asmaa M, Badrawy Hosny, Ibrahim Abeer

机构信息

South Egypt Cancer Institute, Assiut University, EL-Mesak Street, Assiut, Egypt.

出版信息

Int J Clin Oncol. 2014 Aug;19(4):753-60. doi: 10.1007/s10147-013-0615-9. Epub 2013 Sep 26.

DOI:10.1007/s10147-013-0615-9
PMID:24068564
Abstract

BACKGROUND

Chronic myeloid leukemia (CML) is a clonal disease, characterized by a reciprocal t(9, 22) that results in a chimeric BCR/ABL fusion gene. Regulatory T cells (Tregs) constitute the main cell population that enables cancer cells to evade immune surveillance.

OBJECTIVE

The purpose of our study was to investigate the level of Tregs in newly diagnosed CML patients and to correlate it with the patients' clinical, laboratory and molecular data. We also aimed to assess the effect of treatment using tyrosine kinase inhibitor (TKI) on Treg levels.

METHODS

Tregs were characterized and quantified by flow cytometry in 63 newly diagnosed CML patients and 40 healthy controls. TKI was used in 45 patients with chronic phase CML, and the response to therapy was correlated with baseline Treg levels.

RESULTS

The percentages of Tregs were significantly increased in CML patients compared to the controls. Treg numbers were significantly lower in patients with chronic phase CML versus the accelerated and blast phases, and were significantly lower in patients with complete molecular remission (CMR) compared to those patients without CMR.

CONCLUSION

Tregs may play a role in the maintenance of CML. Moreover, the decrease of their levels in patients with CMR suggests that Tregs might have a clinical value in evaluating the effects of therapy.

摘要

背景

慢性髓性白血病(CML)是一种克隆性疾病,其特征为9号和22号染色体相互易位,导致嵌合性BCR/ABL融合基因。调节性T细胞(Tregs)是使癌细胞逃避免疫监视的主要细胞群体。

目的

本研究旨在调查新诊断的CML患者中Tregs的水平,并将其与患者的临床、实验室和分子数据相关联。我们还旨在评估使用酪氨酸激酶抑制剂(TKI)治疗对Treg水平的影响。

方法

通过流式细胞术对63例新诊断的CML患者和40例健康对照者的Tregs进行鉴定和定量。45例慢性期CML患者使用TKI治疗,并将治疗反应与基线Treg水平相关联。

结果

与对照组相比CML患者Tregs的百分比显著增加。慢性期CML患者的Treg数量显著低于加速期和急变期患者;与未达到完全分子缓解(CMR)的患者相比,达到CMR的患者Treg数量显著更低。

结论

Tregs可能在CML维持中发挥作用;此外,CMR患者Treg水平降低表明Tregs在评估治疗效果方面可能具有临床价值。

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本文引用的文献

1
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Indian J Endocrinol Metab. 2012 Nov;16(6):952-7. doi: 10.4103/2230-8210.102998.
2
CD4+ CD25+High Foxp3+ regulatory T cells, B lymphocytes, and T lymphocytes in patients with acute ITP in Assiut Children Hospital.CD4+ CD25+High Foxp3+ 调节性 T 细胞、B 淋巴细胞和 T 淋巴细胞在 Assiut 儿童医院急性 ITP 患者中的变化。
Clin Appl Thromb Hemost. 2014 Jan;20(1):61-7. doi: 10.1177/1076029612454937. Epub 2012 Aug 7.
3
CD4+CD25highFoxP3+ regulatory T-cells in hematologic diseases.
Chimeric antigen-receptor (CAR) engineered natural killer cells in a chronic myeloid leukemia (CML) blast crisis model.
嵌合抗原受体 (CAR) 修饰的自然杀伤细胞在慢性髓细胞白血病 (CML) 急变期模型中的作用。
Front Immunol. 2024 Jan 8;14:1309010. doi: 10.3389/fimmu.2023.1309010. eCollection 2023.
4
Differential inhibition of T-cell receptor and STAT5 signaling pathways determines the immunomodulatory effects of dasatinib in chronic phase chronic myeloid leukemia.达沙替尼通过抑制 T 细胞受体和 STAT5 信号通路来发挥其在慢性期慢性髓性白血病中的免疫调节作用。
Haematologica. 2023 Jun 1;108(6):1555-1566. doi: 10.3324/haematol.2022.282005.
5
Assessment of regulatory T cells (Tregs) and Foxp3 methylation level in chronic myeloid leukemia patients on tyrosine kinase inhibitor therapy.酪氨酸激酶抑制剂治疗的慢性髓性白血病患者中调节性T细胞(Tregs)及Foxp3甲基化水平的评估
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6
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7
Tnfrsf4-expressing regulatory T cells promote immune escape of chronic myeloid leukemia stem cells.表达 Tnfrsf4 的调节性 T 细胞促进慢性髓性白血病干细胞的免疫逃逸。
JCI Insight. 2021 Dec 8;6(23):e151797. doi: 10.1172/jci.insight.151797.
8
The TNF-α/TNFR2 Pathway: Targeting a Brake to Release the Anti-tumor Immune Response.肿瘤坏死因子-α/肿瘤坏死因子受体2通路:靶向一个制动器以释放抗肿瘤免疫反应。
Front Cell Dev Biol. 2021 Oct 12;9:725473. doi: 10.3389/fcell.2021.725473. eCollection 2021.
9
Treatment-Free Remission-A New Aim in the Treatment of Chronic Myeloid Leukemia.无治疗缓解——慢性髓性白血病治疗的新目标。
J Pers Med. 2021 Jul 22;11(8):697. doi: 10.3390/jpm11080697.
10
Immunosuppressive Cell Subsets and Factors in Myeloid Leukemias.髓系白血病中的免疫抑制细胞亚群和因素
Cancers (Basel). 2021 Mar 10;13(6):1203. doi: 10.3390/cancers13061203.
血液系统疾病中的CD4+CD25高表达FoxP3+调节性T细胞
Korean J Lab Med. 2011 Oct;31(4):231-7. doi: 10.3343/kjlm.2011.31.4.231. Epub 2011 Oct 3.
4
Evaluation of monocyte-derived dendritic cells, T regulatory and Th17 cells in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors.酪氨酸激酶抑制剂治疗的慢性髓性白血病患者中单核细胞来源的树突状细胞、调节性T细胞和Th17细胞的评估
Folia Histochem Cytobiol. 2011;49(1):153-60. doi: 10.5603/fhc.2011.0022.
5
Quantitative and functional analyses of CD4(+) CD25(+) FoxP3(+) regulatory T cells in chronic phase chronic myeloid leukaemia patients at diagnosis and on imatinib mesylate.
Br J Haematol. 2011 Apr;153(1):139-43. doi: 10.1111/j.1365-2141.2010.08453.x. Epub 2011 Jan 31.
6
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Exp Hematol. 2010 Dec;38(12):1209-18. doi: 10.1016/j.exphem.2010.09.004. Epub 2010 Sep 18.
7
The role of regulatory T cells in cancer.调节性 T 细胞在癌症中的作用。
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8
Regulatory T cells: major players in the tumor microenvironment.调节性T细胞:肿瘤微环境中的主要参与者。
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9
Reduced circulating CD4+CD25+ cell populations in haemorrhagic fever with renal syndrome.肾综合征出血热患者循环中CD4+CD25+细胞群减少。
Clin Exp Immunol. 2009 Apr;156(1):88-96. doi: 10.1111/j.1365-2249.2008.03858.x. Epub 2008 Dec 11.
10
Imatinib mesylate inhibits CD4+ CD25+ regulatory T cell activity and enhances active immunotherapy against BCR-ABL- tumors.甲磺酸伊马替尼抑制CD4+ CD25+调节性T细胞活性,并增强针对BCR-ABL肿瘤的主动免疫治疗。
J Immunol. 2008 Nov 15;181(10):6955-63. doi: 10.4049/jimmunol.181.10.6955.