期刊文献+

肺癌组织的HLA-Ⅰ类分子表达与临床病理因素关系 被引量:2

Expression of human leukocyte antigen-Ⅰ in lung cancer
下载PDF
导出
摘要 目的研究肺癌组织的人类白细胞抗原I类分子HLA-A,B,C,G的表达情况以及临床病理因素关系。方法抗HLA-A,B,C单克隆抗体(mAb)W6/32,抗HLA-G(mAb)GG11,以免疫组化S-P法检测49例肺癌中的HLA-A,B,C,G抗原表达情况,同时收集肺癌患者临床特征。结果小细胞肺癌、鳞癌和腺癌的HLA-A,B,C抗原表达有不同程度的下降或缺失,小细胞肺癌HLA-A,B,C抗原下降和缺失率最高(P<0.05);而不同病理分期、分级的肺癌HLA-A,B,C抗原表达并无差异(P>0.05)。HLA-G在49例原发肺癌癌细胞中均无阳性表达,但4例肿瘤组织旁的部分免疫细胞上有阳性表达。结论肺癌HLA-A,B,C抗原表达下降与肺癌组织类型相关,而与临床病理因素无关;HLA-G在肺癌细胞无表达,而部分免疫细胞表达HLA-G。 Objective To analyze the association of HLA-A, B, C, G expression status with clinical and pathologic characteristics of lung cancer. Methods Forty-nine tumor samples contained sufficient material were gathered for immunohistochemical analysis. HLA-A, B, C and HLA-G antigens were assayed using monoclonal antibody (W6/32 and GGll) respectively. A database of clinical and pathologic characteristics was established. Results A loss of HIA-A, B, C was obviously observed in cancer tissues, especially in small cell cancers ( P 〈 0.05). HIA G was existed in cancer tissues, but loss in some tumor infiltrating immune cell. No significant correlations were observed among HIA-A, B, C expression and tumor size, nodal involvement ( P 〉 O. 05). Conclusion Different histological types of lung cancer show a different loss of HIA-A,B,C, but loss of HIA-G only in some tumor infiltrating immune cell. HIA-A, B, C expression is not related with clinical and pathologic characteristics. Lung cancer could escape from the host immune system through HIA class I-induced immune tolerance.
出处 《免疫学杂志》 CAS CSCD 北大核心 2008年第1期73-75,78,共4页 Immunological Journal
关键词 HLA-I类分子 肺癌 局部浸润免疫细胞 Human leukocyte antigen class I antigen Lung cancer Tumor infiltrating immune cell
  • 相关文献

参考文献10

  • 1Garridl F, Cabera T, Coneha A, et al. Natural history of HLA expression during tumor development [ J ]. Immunol Today, 1993, 14(3) : 491 - 499.
  • 2Chang CC, Murphy SP, Ferrone S. Differential in vivo and in vitro HLA-G expression in melanoma cells: potential mechanisms [ J ]. Hum Immunol, 2003, 64 ( 11 ) : 1 057 - 1 063.
  • 3Pangauh C,Le Friec G, Caulet MS, et al. Lung macrophages and dendritic cells express HLA-G mole c2ules in pulmonary diseases [J]. Hum Immunol,2002,63(2) :83 - 90.
  • 4Doyle A, Martini J, Fana K, et al. Markedly decreased expression of class Ⅰ histocom-patibility antigens, protein and mRNA in human small-cell lung cancer[ J]. J Exp Med, 1985,161(6): 1 135-1 151.
  • 5Korkolopoulou P, Kaklamanis L, Pezzella F, et al. loss of antigen-presenting molecules (MHC class Ⅰ and TAP-1 ) in lung cancer [J]. Br J Cancer, 1996, 73(2) : 148 - 153.
  • 6Redondo M, Ruiz Cabello F, Concha A, et al. Altered HIA class I expression in non-small cell lung cancer is independent of c-myc activation [ J ]. Cancer Res, 1991, 51(9):2463-2468.
  • 7UICC. Lunge[A]//UICC ed. Report of TNM-prognostic factors project committee meeting[ R]. Geneva; Switzerland, 1997: 14- 15.
  • 8Ramnath N, Tan D, Li D, et al. Is downregulation of MHC class Ⅰ antigen expression in human non-small cell lung cancer associated with prolonged survival [ J ]. Cancer Immunol Immunother,2006,55(8) :891 - 899.
  • 9李文广,姚庆祥,畅继武.HLA-Ⅰ类分子与肿瘤逃逸[J].医学综述,2003,9(6):325-327. 被引量:1
  • 10Urosevic M, Kurrer MO, Kamarashev J, et al. Human leukocyte antigen G up-regulation in lung cancer associates with high-grade histology, human leukocyte antigen class Ⅰ loss and interleukin-10 production [ J ]. Am J Pathol, 2001, 159(3) :817 - 824.

二级参考文献19

  • 1Groettrup M, Soza A, Kuckelkorn U, et al. Peptide antigen production by the protea- some; complexity provides eficiency [J]. Immunol Today, 1996,17(9) :429-435.
  • 2Roelse J,Gromme M,Momburg F, et al. Trimming of TAP-translocated peptides in the endoplasmic reticulum and in the cytosol during recycling. [J] . Exp Med, 1994,180(5) : 1591-1597.
  • 3Ortmann B,Copeman J, Lehner PJ.A Critical Role for Tapasin in the Assembly and Function of Multimeric MHC I TAP Complexes[ J] .Science, 1997,277 (5330) : 1306-1309.
  • 4Wei ML,Cresswell P. HLA-A2 Molecules in an antigen-processing mutant cell contain signal sequence-derived peptides[J]. Nature, 1992,356(6368) :443-446.
  • 5Garrido F, Ruiz-Cabello F, Cabrera T, et al. Implication for immunnosurveillance of altered HLA class I phenotypes in human tumors[J].Immunol Today, 1997,18 (2) : 89-95.
  • 6Torres MJ,Ruiz-Cabello F,Skopdy A,et al.Loss of an HLA haplotype in pancease cancer tissue and its corresponding tumor derived cell line.[J] .Tissue Antigen. 1996,47(5) :372-381.
  • 7Ruiz-Cabello F, Garrido F. HLA and cancer: from research to clinical impact[ J]. Immunol Today, 1998,19(12) : 539-542.
  • 8Browning M, Kransa P. Genetic diversity of HLA-A2: evolutionary and functional significance[J]. Immunology Today, 1996,17(4) : 165-170.
  • 9Sidney J, Grey HM, Kubo RT, et al. Practical, biochemical and evolutionary implication of the discovery of HLA class I supermotifs[ J]. Immunology today, 1996,17 (6) : 261-266.
  • 10Restifo NP, Esquivel F, Kawakami Y, et al. Identification of human cancers defi- cient in antigen processing[ J]. Exp Med, 1993,177 (2) :265-272.

同被引文献27

  • 1刘华,马文丽,郑文岭.GEO(Gene Expression Omnibus):高通量基因表达数据库[J].中国生物化学与分子生物学报,2007,23(3):236-244. 被引量:9
  • 2Giardina SL, Anderson SK, Sayers TJ, et al. Selective loss of NK cytotoxicity in antisense NK-TR1 rat LGL cell lines. Abrogation of antibody-independent tumor and virusinfected target cell killing [J]. J Immunol, 1995, 154 (1): 80-87.
  • 3Kubach J, Lutter P, Bopp T, et al. Human CD4+CD25+ regulatory T cells: proteome analysis identifies galectin-10 as a novel marker essential for their anergy and suppressive function [J]. Blood, 2007, 110 (5): 1550-1558.
  • 4Evans PC, Smith TS, Lai MJ, et al. A novel type of deubiquitinating enzyme [J]. J Biol Chem, 2003, 278 (25): 23180-23186.
  • 5Zitvogel L, Tesniere A, Kroemer G. Cancer despite immunosurveillance: immunoselection and immunosubversion [J]. Nat Rev Immunol, 2006, 6 (10): 715-727.
  • 6Galon J, Costes A, Sanchez Cabo F, et al. Type, density, and location of immune cells within human colorectal tumors predict clinical outcome [J]. Science, 2006, 313 (5795): 1960-1964.
  • 7Dejean AS, Beisner DR, Ch'en IL. et al. Transcription factor Foxo3 controls the magnitude of T cell immune responses by modulating the function of dendritic cells [J]. Nat Immunol, 2009, 10 (5): 504-513.
  • 8Manicassamy S, Reizis B, Ravindran R, et al. Activation of β-catenin in dendritic cells regulates immunity versus tolerance in the intestine [J]. Science, 2010, 329 (5993): 849-853.
  • 9Grivennikov SI, Greten FR, Karin M. Immunity, inflammation, and cancer [J]. Cell, 2010, 140 (6): 883-899.
  • 10Guo F, Hildeman D, Tripathi P, et al. Coordination of IL-7 receptor and T-cell receptor signaling by cell-division cycle 42 in T-cell homeostasis [J]. Proc Natl Sci USA, 2010, 107 (43): 18505-18510.

引证文献2

二级引证文献5

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部