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胃淋巴上皮瘤样癌中免疫相关调节因子分析 被引量:5

Analysis of immune regulatory factors in lymphoepithelioma-like gastric carcinoma
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摘要 目的分析胃淋巴上皮瘤样癌(LELGC)肿瘤微环境中肿瘤浸润淋巴细胞表型及程序性死亡分子-1(PD-1)/程序性死亡分子配体-1(PD-L1)的特点。方法分析4例LELGC患者的临床特征,对肿瘤石蜡组织免疫组织化学法检测CD3、CD4、CD8、CD20、Foxp3、PD-1、PD-L1,原位杂交法检测EB病毒编码RNA(EBER)。结果 4例肿瘤组织EBER均阳性,肿瘤浸润淋巴细胞以CD8阳性细胞为主。所有病例中PD-L1均高表达,其中2例以肿瘤浸润淋巴细胞表达为主,另2例以肿瘤细胞表达为主。结论 LELGC肿瘤微环境具有肿瘤浸润淋巴细胞丰富、PD-L1高表达等特点。PD-1/PD-L1抑制剂或许是治疗LELGC的一个有效手段。 Objective To investigate the features of the tumor infiltrating lymphocyte immunophenotype, programmed death ligand-1 and programmed death ligand-1 in lymphoepithelioma-like gastric carcinoma (LELGC). To discuss the theoretical foundations of using PD-1/PD-L1 inhibitors in LELGC. Method The clinical and histological data of four patients with LELGC were retrospectively analyzed. The expression of CD3, CD4, CDS, CD20, Foxp3, PD-1, PD- L1 in tumor microenvironment was detected by immunohistochemical methods. The Epstein-Barr virus-encoded small RNA(EBER) was detected by in situ hybridization. Result EBER was positive in all four tumors. The immunohisto- chemical examination indicated that the CD3 positive lymphocytes were much more than the CD20 positive lympho- cytes, especially the CD8 positive lymphocytes. Foxp3 positive lymphocytes are rare. The PD-L1 was over-expressed ( about 50% - 70% ) in all four tumors. The PD-L1 was expressed by tumor infiltrating lymphocytes in two tumors and by tumor cells in the other two tumors. The expression of PD-1 was about 10% - 20%. Conclusion There are a- bundant tumor infiltrating lymphocytes and over-expression of PD-L1 in the tumor microenvironment of LELGC. The inhibitors of PD-1/PD-L1 may be an effective treatment for the LELGC patients.
出处 《中国临床医生杂志》 2017年第6期25-29,共5页 Chinese Journal For Clinicians
基金 北京医院院级课题项目(BJ-2015-125)
关键词 胃肿瘤 淋巴上皮瘤样癌 肿瘤浸润淋巴细胞 程序性死亡分子-1 程序性死亡分子配体-1 Gastric cancer Lymphoepithelioma-like carcinoma Tumor infiltrating lymphocytes Programmed death-1 Programmed death ligand-1
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  • 1胡亚美 江载芳.诸福棠实用儿科学[M]第7版[M].北京:人民卫生出版社,2002.1514. 被引量:1201
  • 2Okano M, Kaka K, Kimura H, et al. Proposed guidelines for diag-nosing chronic active Epstein-Barr virus infection [ J ]. Am J Hemo-tol, 2005 , 80(1) :64-69. 被引量:1
  • 3Gulley ML, Tang W. Laboratory assays for Epstein-Barr virus-relat-ed disease [J]. J Mol Diagn, 2008,10(4) :279-292. 被引量:1
  • 4Klutts JS, Ford BA, Perez NR, et al. Evidence-based approach forinterpretation of Epstein-Barr virus serological patterns [ J ]. J ClinMicrobiol, 2009, 47(10) :3204-3210. 被引量:1
  • 5Delecluse HJ, Feederle R,0’ Sullivan B, et al. Epstein Barr virus-associated tumours : An update for the attention of the working pa-thologist [J]. J Clin Pathol, 2007, 60(12) =1358-1364. 被引量:1
  • 6Antonino C, Annunziata G, Giampietro D. EBV-Associated lympho-proliferative disorders: classification and treatment [ J]. The Oncolo-gist, 2008,13(5) =577-585. 被引量:1
  • 7Vine LJ, Shepherd K, Hunter JG, et al. Characteristics of Epstein-Barr virus hepatitis among patients with jaundice or acute hepatitis[J]. Aliment Pharmacol The, 2012, 36( 1 ) :16-21. 被引量:1
  • 8Yin CC, Medeiros LJ, Abruzzo LV, et al. EBV-associated B-and T-cell posttransplant lymphoproliferative disorders following primaryEBV infection in a kidney transplant recipient [ J ]. Am J ClinPathol, 2005, 123(2) :222-228. 被引量:1
  • 9S6nchez F,Gimeno-Bayon JL,Esgueva R,et al. Fatal liver failure:molecular evidence for chronic active Epstein-Barr virus infection[J], Ann Diagn Pathol, 2008, 12(5) :368-371. 被引量:1
  • 10Savoldo B, Huls MH, Liu Z, et al. Autologous Epstein-Barr virus(EBV) -specific cytotoxic T cells for the treatment of persistent activeEBV infection[J]. Blood 2003, 100(12) :4059-4066. 被引量:1

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