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本文引用的文献

1
FOXP3+ regulatory T cells in the human immune system.FOXP3+ 调节性 T 细胞在人类免疫系统中的作用。
Nat Rev Immunol. 2010 Jul;10(7):490-500. doi: 10.1038/nri2785. Epub 2010 Jun 18.
2
Monocyte chemoattractant protein-1 is generated via TGF-beta by myofibroblasts in gastric intestinal metaplasia and carcinoma without H. pylori infection.单核细胞趋化蛋白-1 通过 TGF-β由无 H. pylori 感染的胃肠化生和癌中的肌纤维母细胞产生。
Cancer Sci. 2010 Aug;101(8):1783-9. doi: 10.1111/j.1349-7006.2010.01609.x. Epub 2010 Apr 29.
3
Distribution of Th17 cells and FoxP3(+) regulatory T cells in tumor-infiltrating lymphocytes, tumor-draining lymph nodes and peripheral blood lymphocytes in patients with gastric cancer.胃癌患者肿瘤浸润淋巴细胞、肿瘤引流淋巴结和外周血淋巴细胞中 Th17 细胞和 FoxP3(+)调节性 T 细胞的分布。
Cancer Sci. 2010 Sep;101(9):1947-54. doi: 10.1111/j.1349-7006.2010.01624.x.
4
Distribution of Foxp3-, CD4- and CD8-positive lymphocytic cells in benign and malignant prostate tissue.Foxp3、CD4 和 CD8 阳性淋巴细胞在良性和恶性前列腺组织中的分布。
APMIS. 2010 May;118(5):360-5. doi: 10.1111/j.1600-0463.2010.02604.x.
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Pathology of gastric intestinal metaplasia: clinical implications.胃肠化生的病理学:临床意义
Am J Gastroenterol. 2010 Mar;105(3):493-8. doi: 10.1038/ajg.2009.728.
6
Elevated expression of Foxp3 in tumor-infiltrating Treg cells suppresses T-cell proliferation and contributes to gastric cancer progression in a COX-2-dependent manner.肿瘤浸润调节性 T 细胞中 Foxp3 的高表达抑制 T 细胞增殖,并以 COX-2 依赖的方式促进胃癌的进展。
Clin Immunol. 2010 Mar;134(3):277-88. doi: 10.1016/j.clim.2009.10.005. Epub 2009 Nov 8.
7
The number of Foxp3-positive regulatory T cells is increased in Helicobacter pylori gastritis and gastric cancer.Foxp3 阳性调节 T 细胞在幽门螺杆菌胃炎和胃癌中增多。
Pathol Res Pract. 2010 Jan 15;206(1):34-8. doi: 10.1016/j.prp.2009.07.019. Epub 2009 Oct 12.
8
Coadaptation of Helicobacter pylori and humans: ancient history, modern implications.幽门螺杆菌与人类的共同适应:古老历史,现代影响。
J Clin Invest. 2009 Sep;119(9):2475-87. doi: 10.1172/JCI38605.
9
FOXP3-expressing CD4(+) T-cell numbers increase in areas of duodenal gastric metaplasia and are associated to CD4(+) T-cell aggregates in the duodenum of Helicobacter pylori-infected duodenal ulcer patients.在十二指肠胃化生区域,表达FOXP3的CD4(+) T细胞数量增加,且与幽门螺杆菌感染的十二指肠溃疡患者十二指肠中的CD4(+) T细胞聚集物相关。
Helicobacter. 2009 Jun;14(3):192-201. doi: 10.1111/j.1523-5378.2009.00673.x.
10
Effect of Helicobacter pylori eradication on incidence of gastric cancer in human and animal models: underlying biochemical and molecular events.幽门螺杆菌根除对人类和动物模型胃癌发病率的影响:潜在的生化和分子事件
Helicobacter. 2009 Jun;14(3):159-71. doi: 10.1111/j.1523-5378.2009.00677.x.

Foxp3 阳性调节性 T 细胞在胃炎、消化性溃疡和胃腺癌中的数量增加。

Increased numbers of Foxp3-positive regulatory T cells in gastritis, peptic ulcer and gastric adenocarcinoma.

机构信息

Department of Life Sciences, Institute of Molecular and Cellular Biology, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

World J Gastroenterol. 2012 Jan 7;18(1):34-43. doi: 10.3748/wjg.v18.i1.34.

DOI:10.3748/wjg.v18.i1.34
PMID:22228968
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3251803/
Abstract

AIM

To determine the number of regulatory T cells (Tregs) in gastric mucosa of patients with gastritis, peptic ulcers and gastric cancer.

METHODS

This study was a retrospective analysis of gastric antrum biopsy specimens from healthy controls (n = 22) and patients with gastritis (n = 30), peptic ulcer (n = 83), or gastric cancer (n = 32). Expression of CD4, CD25 and Foxp3 was determined by immunohistochemistry in three consecutive sections per sample.

RESULTS

Compared with healthy controls, there was an increased number of CD25(+) and Foxp3(+) cells in patients with gastritis (P = 0.004 and P = 0.008), peptic ulcer (P < 0.001 and P < 0.001), and gastric cancer (P < 0.001 and P < 0.001). The ratio of CD25(+)/CD4(+) or Foxp3(+)/CD4(+) cells was also significantly higher in all disease groups (P < 0.001, respectively). The number of CD4(+), CD25(+), and Foxp3(+) cells, and the ratio of CD25(+)/CD4(+) and Foxp3(+)/CD4(+) cells, were associated with the histological grade of the specimens, including acute inflammation, chronic inflammation, lymphoid follicle number, and Helicobacter pylori infection. The number of CD4(+), CD25(+) and Foxp3(+) cells, and the ratio of CD25(+)/CD4(+) and Foxp3(+)/CD4(+) cells, were negatively associated with intestinal metaplasia among gastritis (P < 0.001, P < 0.001, P < 0.001, P = 0.002 and P = 0.002) and peptic ulcer groups (P = 0.013, P = 0.004, P < 0.001, P = 0.040 and P = 0.003).

CONCLUSION

Tregs are positively associated with endoscopic findings of gastroduodenal diseases and histological grade but negatively associated with intestinal metaplasia in gastritis and peptic ulcer groups.

摘要

目的

确定胃炎、消化性溃疡和胃癌患者胃黏膜中调节性 T 细胞(Tregs)的数量。

方法

本研究回顾性分析了 22 例健康对照者(对照组)和 30 例胃炎、83 例消化性溃疡和 32 例胃癌患者的胃窦活检标本。采用免疫组织化学法检测每例标本 3 个连续切片中 CD4、CD25 和 Foxp3 的表达。

结果

与对照组相比,胃炎(P=0.004 和 P=0.008)、消化性溃疡(P<0.001 和 P<0.001)和胃癌(P<0.001 和 P<0.001)患者的 CD25+和 Foxp3+细胞数量增加。所有疾病组 CD25+/CD4+或 Foxp3+/CD4+细胞的比值也显著升高(分别为 P<0.001)。CD4+、CD25+和 Foxp3+细胞的数量,以及 CD25+/CD4+和 Foxp3+/CD4+细胞的比值与标本的组织学分级有关,包括急性炎症、慢性炎症、淋巴滤泡数量和幽门螺杆菌感染。CD4+、CD25+和 Foxp3+细胞的数量,以及 CD25+/CD4+和 Foxp3+/CD4+细胞的比值与胃炎(P<0.001、P<0.001、P<0.001、P=0.002 和 P=0.002)和消化性溃疡组(P=0.013、P=0.004、P<0.001、P=0.040 和 P=0.003)的肠上皮化生呈负相关。

结论

Tregs 与胃十二指肠疾病的内镜发现和组织学分级呈正相关,但与胃炎和消化性溃疡组的肠上皮化生呈负相关。