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本文引用的文献

1
Clinical significance and functional studies of myeloid-derived suppressor cells in chronic hepatitis C patients.慢性丙型肝炎患者骨髓来源抑制性细胞的临床意义及功能研究。
J Clin Immunol. 2013 May;33(4):798-808. doi: 10.1007/s10875-012-9861-2. Epub 2013 Jan 26.
2
Treating hepatitis C infection by targeting the host.针对宿主治疗丙型肝炎感染。
Transl Res. 2012 Jun;159(6):421-9. doi: 10.1016/j.trsl.2011.12.007. Epub 2012 Jan 10.
3
Myeloid suppressor cells induced by hepatitis C virus suppress T-cell responses through the production of reactive oxygen species.丙型肝炎病毒诱导的髓源性抑制细胞通过产生活性氧抑制 T 细胞反应。
Hepatology. 2012 Feb;55(2):343-53. doi: 10.1002/hep.24700.
4
Myeloid-derived suppressor cell inhibition of the IFN response in tumor-bearing mice.肿瘤荷瘤小鼠中髓源性抑制细胞对 IFN 反应的抑制作用。
Cancer Res. 2011 Aug 1;71(15):5101-10. doi: 10.1158/0008-5472.CAN-10-2670. Epub 2011 Jun 16.
5
Virus-induced tumor inflammation facilitates effective DC cancer immunotherapy in a Treg-dependent manner in mice.病毒诱导的肿瘤炎症以依赖 Treg 的方式促进了小鼠中有效的 DC 癌症免疫治疗。
J Clin Invest. 2011 Jul;121(7):2570-82. doi: 10.1172/JCI45585. Epub 2011 Jun 6.
6
Elevated myeloid-derived suppressor cells in pancreatic, esophageal and gastric cancer are an independent prognostic factor and are associated with significant elevation of the Th2 cytokine interleukin-13.在胰腺癌、食管癌和胃癌中,髓源性抑制细胞的升高是一个独立的预后因素,并且与 Th2 细胞因子白细胞介素-13 的显著升高相关。
Cancer Immunol Immunother. 2011 Oct;60(10):1419-30. doi: 10.1007/s00262-011-1028-0. Epub 2011 Jun 5.
7
Distinct myeloid suppressor cell subsets correlate with plasma IL-6 and IL-10 and reduced interferon-alpha signaling in CD4⁺ T cells from patients with GI malignancy.不同的髓系抑制细胞亚群与胃肠道恶性肿瘤患者 CD4+T 细胞中血浆 IL-6 和 IL-10 相关,并降低干扰素-α信号转导。
Cancer Immunol Immunother. 2011 Sep;60(9):1269-79. doi: 10.1007/s00262-011-1029-z. Epub 2011 May 21.
8
Interleukin-6 induces Gr-1+CD11b+ myeloid cells to suppress CD8+ T cell-mediated liver injury in mice.白细胞介素 6 诱导 Gr-1+CD11b+ 髓样细胞抑制小鼠 CD8+ T 细胞介导的肝损伤。
PLoS One. 2011 Mar 4;6(3):e17631. doi: 10.1371/journal.pone.0017631.
9
Hepatic stellate cells regulate immune response by way of induction of myeloid suppressor cells in mice.肝星状细胞通过诱导小鼠髓源性抑制细胞来调节免疫反应。
Hepatology. 2011 Mar;53(3):1007-19. doi: 10.1002/hep.24162.
10
Myeloid derived suppressor cells in human diseases.髓系来源的抑制细胞在人类疾病中的作用。
Int Immunopharmacol. 2011 Jul;11(7):802-7. doi: 10.1016/j.intimp.2011.01.003. Epub 2011 Jan 13.

慢性丙型肝炎患者接受4周抗病毒治疗后,外周血中髓源性抑制细胞的扩增减少。

Expansion of myeloid-derived suppressor cells from peripheral blood decreases after 4-week antiviral treatment in patients with chronic hepatitis C.

作者信息

Liu Ying, She Lan-Hui, Wang Xiang-Yang, Zhang Geng-Lin, Yan Ying, Lin Chao-Shuang, Zhao Zhi-Xin, Gao Zhi-Liang

机构信息

Department of Infectious Diseases, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.

Intranet of Guangzhou Woman and Children's Medical Center Guangzhou, China.

出版信息

Int J Clin Exp Med. 2014 Apr 15;7(4):998-1004. eCollection 2014.

PMID:24955173
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4057852/
Abstract

Myeloid-derived suppressor cells (MDSCs) are one of the most important regulators of anti-tumor T-cell responses in cancers. This study aimed to investigate MDSCs in the peripheral blood of patients with chronic hepatitis C (CHC) before and after 4-week treatment with pegylated interferon (PEG-IFN) and ribavirin, and to evaluate their correlation with CD4(+)CD25(high) regulatory T cells (Tregs) and clinical parameters. A total of 80 patients with CHC were enrolled into this study, 37 of whom were treated with PEG-IFN and ribavirin. Compared with healthy controls (0.462% [range 0.257%-0.634%]), the proportion of MDSCs in the peripheral blood of 80 CHC patients (0.601% [range 0.333%-1.027%]) increased significantly before therapy (P=0.011). For 37 HCV patients, the proportion of circulating MDSCs (0 w: 0.597% [range 0.296%-1.021%], 4 w: 0.126% [0.066%-0.239%], P<0.01) and Tregs (0 w: 2.467±0.927%, 4 w: 2.074±0.840%, P=0.047) decreased significantly after 4-week antiviral treatment. No significant correlation was found between MDSCs and Tregs. These findings suggest that MDSCs expand in the peripheral blood of CHC patients, but decrease after 4-week antiviral treatment.

摘要

髓源性抑制细胞(MDSCs)是癌症中抗肿瘤T细胞反应的最重要调节因子之一。本研究旨在调查慢性丙型肝炎(CHC)患者在接受聚乙二醇干扰素(PEG-IFN)和利巴韦林治疗4周前后外周血中的MDSCs,并评估它们与CD4(+)CD25(high)调节性T细胞(Tregs)及临床参数的相关性。共有80例CHC患者纳入本研究,其中37例接受PEG-IFN和利巴韦林治疗。与健康对照者(0.462%[范围0.257%-0.634%])相比,80例CHC患者治疗前外周血中MDSCs的比例(0.601%[范围0.333%-1.027%])显著升高(P=0.011)。对于37例丙型肝炎病毒(HCV)患者,抗病毒治疗4周后,循环MDSCs的比例(0周:0.597%[范围0.296%-1.021%],4周:0.126%[0.066%-0.239%],P<0.01)和Tregs的比例(0周:2.467±0.927%,4周:2.074±0.840%,P=0.047)显著降低。未发现MDSCs与Tregs之间存在显著相关性。这些发现表明,MDSCs在CHC患者外周血中增多,但在抗病毒治疗4周后减少。