Immunohistochemical localization of programmed death-1 ligand-1 (PD-L1) in gastric carcinoma and its clinical significance

被引:462
作者
Wu, Changping
Zhu, Yibei
Jiang, Jingting
Zhao, Jiemin
Zhang, Xue-Guang
Xu, Ning [1 ]
机构
[1] Lund Univ, Inst Lab Med, Sect Clin Chem & Pharmacol, S-22185 Lund, Sweden
[2] Suzhou Univ, Inst Biotechnol, Suzhou 215007, Peoples R China
[3] Suzhou Univ, Affiliated Hosp 3, Changzhou 213003, Peoples R China
关键词
programmed death-1 ligand-1; PD-L1; gastric carcinoma; immunohistochemistry; prognostic marker;
D O I
10.1016/j.acthis.2006.01.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present study examined programmed death-1 ligand-1 (PD-L1) detected by immunohistochemical. labeling in 102 cases of human gastric carcinoma, 10 adenoma and 10 normal tissues. The relationship between PD-L1 immunolocalization and clinical pathological features, as well as the prognosis of gastric carcinoma, was explored. There was no PD-L1 detectable in normal gastric tissues and very weak immunolabeling in gastric adenomas, but it could be detected in 42.2% of gastric carcinoma tissues. There was no correlation between PD-L1 immunolocalization and patient age, sex, tumor location or the degree of tumor differentiation in the gastric carcinomas. However, PD-L1 immunodetection was significantly correlated to tumor size, invasion, lymph node metastasis and survival time of patients. PD-L1 immunolabeling was significantly enhanced (P<0.01) when the tumor infiltrated into the deep muscular layers, with lymph node metastasis or survival time of less than 2 years, Moreover, multivariate analysis demonstrated that PD-L1 immunodetection could be used as an independent factor to evaluate the prognosis of gastric carcinoma. (C) 2006 Elsevier GmbH. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
相关论文
共 21 条
[1]   Immunobiology of dendritic cells [J].
Banchereau, J ;
Briere, F ;
Caux, C ;
Davoust, J ;
Lebecque, S ;
Liu, YT ;
Pulendran, B ;
Palucka, K .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :767-+
[2]   Blockade of programmed death-1 Ligands on dendritic cells enhances T cell activation and cytokine production [J].
Brown, JA ;
Dorfman, DM ;
Ma, FR ;
Sullivan, EL ;
Munoz, O ;
Wood, CR ;
Greenfield, EA ;
Freeman, GJ .
JOURNAL OF IMMUNOLOGY, 2003, 170 (03) :1257-1266
[3]   Costimulatory regulation of T cell function [J].
Chambers, CA ;
Allison, JP .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (02) :203-210
[4]  
Chen Zengchun, 2000, Zhonghua Zhongliu Zazhi, V22, P311
[5]   Blockade of B7-H1 improves myeloid dendritic cell-mediated antitumor immunity [J].
Curiel, TJ ;
Wei, S ;
Dong, HD ;
Alvarez, X ;
Cheng, P ;
Mottram, P ;
Krzysiek, R ;
Knutson, KL ;
Daniel, B ;
Zimmermann, MC ;
David, O ;
Burow, M ;
Gordon, A ;
Dhurandhar, N ;
Myers, L ;
Berggren, R ;
Hemminki, A ;
Alvarez, RD ;
Emilie, D ;
Curiel, DT ;
Chen, LP ;
Zou, WP .
NATURE MEDICINE, 2003, 9 (05) :562-567
[6]  
Dong HD, 1999, NAT MED, V5, P1365
[7]  
Dong HD, 2002, NAT MED, V8, P793, DOI 10.1038/nm730
[8]   Dendritic cells in cancer immunotherapy [J].
Fong, L ;
Engleman, EG .
ANNUAL REVIEW OF IMMUNOLOGY, 2000, 18 :245-273
[9]   Involvement of PD-L1 on tumor cells in the escape from host immune system and tumor immunotherapy by PD-L1 blockade [J].
Iwai, Y ;
Ishida, M ;
Tanaka, Y ;
Okazaki, T ;
Honjo, T ;
Minato, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (19) :12293-12297
[10]   B7-H1 is expressed by human endothelial cells and suppresses T cell cytokine synthesis [J].
Mazanet, MM ;
Hughes, CCW .
JOURNAL OF IMMUNOLOGY, 2002, 169 (07) :3581-3588