期刊文献+

共刺激分子PD-L1在鼻咽癌组织中的表达和意义 被引量:3

Expression and significance of costimulatory molecule PD-L1 in nasopharyngeal carcinoma
原文传递
导出
摘要 目的探讨共刺激分子PD-L1在鼻咽癌组织的表达和临床意义,以及PD-L1的表达和鼻咽癌Foxp3+淋巴细胞增多的相关性。方法采用免疫组化方法检测共刺激分子PD-L1在64例鼻咽癌的肿瘤组织和20例慢性鼻咽炎组织的表达情况及Foxp3+淋巴细胞的分布。结果 PD-L1在鼻咽癌组织中阳性表达率为67.2%,明显高于其在慢性鼻咽炎组织中的表达,差异具有统计学意义(P<0.05)。PD-L1的阳性表达与鼻咽癌病人性别、年龄、临床分期及是否转移等指标均无显著相关性(P>0.05),但与鼻咽癌组织中Foxp3+淋巴细胞增加有关,差异有统计学意义(P<0.05),并且鼻咽癌PD-L1的表达也与Foxp3+/CD8+淋巴细胞比率增加正相关(P<0.05)。结论鼻咽癌组织PD-L1在鼻咽癌组织中高表达,并与瘤内的调节性T细胞升高及CD8+细胞下降有关,其可能在鼻咽癌的发展中起到一定作用,有望成为免疫治疗的一个新靶点。 Objective To investigate the expression and significance of PD-L1 and explore the relationship between PD-L1 protein expression and the Foxp3 expression in nasopharyngeal carcinoma (NPC). Methods Immunohistochemistry method was used to detect PD-L1 and Foxp3 expression in 64 nasopharyngeal carcinomas and 20 chronic nasopharyngitis. Results Comparing with chronic nasopharyngitis, PD-L1 were increased in NPC specimens (P0.05), but it was not significantly correlated with gender, age, lymph node metastasis and clinical stage (P0.05). The lymphocytes with Foxp3 in NPC were also increased (P0.05), and the density of Foxp3+ TIL was positively associated with PD-L1 (P0.05). The ratio of Foxp3+ / CD8+ TIL was significantly up-regulated in PD-L1+ nasopharyngeal carcinoma compare to PD-L1- nasopharyngeal carcinoma (P0.05). Conclusion These results suggest that PD-L1 may play a role in immune evasion of nasopharyngeal carcinoma and may be considered as a new therapy target.
出处 《热带医学杂志》 CAS 2012年第2期154-156,F0004,共4页 Journal of Tropical Medicine
基金 广东省自然科学基金(8451008901000710) 广东省医学科研基金(A2008156 A2008141)
关键词 鼻咽癌 PD-L1 FOXP3 nasopharyngeal carcinoma PD-L1 Foxp3
  • 相关文献

参考文献3

二级参考文献25

共引文献13

同被引文献39

  • 1中华医学会感染病学分会艾滋病学组.艾滋病诊疗指南(2011版)[J].中华临床感染病杂志,2011,4(6). 被引量:379
  • 2Hull MW, Phillips P, Montaner JS. Changing global epidemiology of pulmonary manifestations of HIV/AIDS[J]. Chest, 2008, 134(6) : 1287-1298.
  • 3Saresella M, Rainone V, A1-Daghri NM, et al. The PD-1/PD- L1 pathway in human pathology[J]. Curt Mol Med, 2012, 12 (3) : 259-267.
  • 4Jin HT, Ahmed R, Okazaki T. Role of PD-1 in regulating T- cell immunity [J]. Curr Top Microbiol Immunol,2011, 350: 17-37.
  • 5Blank C,Maekensen &Contribution of the PD-L1/PD-1 pathway to T-cell exhaustion: an update on implications for chronic infections and tumor evasion [J]. Cancer Immunol Immunother, 2007, 56(5) :739-745.
  • 6Walker-Sperling VE, Buckheit RW 3rd, Blankson JN. Comparative Analysis of the Capacity of Elite Suppressor CD4+ and CD8+ T Ceils To Inhibit HIV-1 Replication in Monocyte- Derived Macrophages [ J ]. J Virol, 2014,88 ( 17 ) : 9789-9798.
  • 7Boni C, Fisicaro P, Valdatta C,et al. Characterization of hepatitis B virus (HBV)-specific T-cell dysfunction in chronic HBV infection[J]. J Virol, 2007, 81(8):4215-4225.
  • 8Bandaru A, Devalraju KP, Paidipally P, et al.Phosphorylated STAT3 and PD-1 regulate IL-17 production and IL-23 receptor expression in Mycohacterium tuberculosis infection[J ].Eur JImmunol, 2014,44(7) :2013-2024.
  • 9Jurado JO, Alvarez JB, Pasquinelli V, et al. Programmed death (PD)-l:PD-ligand 1/PD-ligand 2 pathway inhibits T cell effector functions during human tuberculosis [J].The Journal of Immunology, 2008,181 : 116-125.
  • 10Ishida Y,Agata Y,Shibahara K,et al.Induced expression of PD-1,a novel member of the immunoglobulin gene superfamily,upon programmed cell death[J].EMBO J,1992,11(11):3887-3895.

引证文献3

二级引证文献16

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