Prognostic significance of cytokine modulation in non-small cell lung cancer

被引:45
作者
Neuner, A
Schindel, M
Wildenberg, U
Muley, T
Lahm, H
Fischer, JR
机构
[1] Thoraxklin Heidelberg GGMBH, Immunol Mol Biol Lab, D-69126 Heidelberg, Germany
[2] Thoraxklin Heidelberg GGMBH, Dept Surg, D-69126 Heidelberg, Germany
[3] Thoraxklin Heidelberg GGMBH, Dept Med Oncol, D-69126 Heidelberg, Germany
关键词
non-small cell lung cancer; immunosuppression; interleukin-2; interleukin-10; tumor-derived factors; prognosis;
D O I
10.1002/ijc.10604
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increased production of immunosuppressive interleukin-10 (IL-10) by non-small cell lung cancer (NSCLC) and increased serum IL-10 concentrations in NSCLC-patients have recently been correlated to reduced survival. We earlier demonstrated suppression of IL-2 secretion in whole blood cell cultures of NSCLC-patients. We now analyzed the influence of IL-2 secretion on survival in NSCLC-patients and the influence of IL-10 on IL-2 secretion. The correlation of the IL-2 producing ability of whole blood cells in response to PHA in 90 NSCLC-patients at the time of diagnosis to survival was calculated by Crit-level, the Kaplan-Meier method and the log-rank test. With a cut-off value of IL-2 production of 1, 100 pg/ml by whole blood cells the difference in survival was significant with a p-value of 0.014. In the group with high and low IL-2, median survival was 14.1 and 9.7 months, respectively. In the subgroup of 33 surgically-treated patients the difference in survival was significant with a p-value of 0.011. In 14 patients with surgical resection of the tumor and high IL-2 at diagnosis and 19 patients with surgical resection, but low IL-2 at diagnosis, median survival was 86.2 and 11.3 months, respectively. Secretion of IL-2 in whole blood cell cultures from healthy individuals was inhibited in a dose-dependent manner upon addition of IL-10. Taken together, suppression of IL-2 secretion has prognostic significance for survival of NSCLC-patients and may be mediated by tumor-derived IL-10. (C) 2002 Wiley-Liss, Inc.
引用
收藏
页码:287 / 292
页数:6
相关论文
共 41 条
[21]   INTERLEUKIN-10, A NOVEL B-CELL STIMULATORY FACTOR - UNRESPONSIVENESS OF X-CHROMOSOME LINKED IMMUNODEFICIENCY-B CELLS [J].
GO, NF ;
CASTLE, BE ;
BARRETT, R ;
KASTELEIN, R ;
DANG, W ;
MOSMANN, TR ;
MOORE, KW ;
HOWARD, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1625-1631
[22]   Clinical implications of interleukin (IL)-10 induced by non-small-cell lung cancer [J].
Hatanaka, H ;
Abe, Y ;
Kamiya, T ;
Morino, F ;
Nagata, J ;
Tokunaga, T ;
Oshika, Y ;
Suemizu, H ;
Kijima, H ;
Tsuchida, T ;
Yamazaki, H ;
Inoue, H ;
Nakamura, M ;
Ueyama, Y .
ANNALS OF ONCOLOGY, 2000, 11 (07) :815-819
[23]  
Huang M, 1998, CANCER RES, V58, P1208
[24]  
HUANG M, 1995, CANCER RES, V55, P3847
[25]  
Huang M, 1996, J IMMUNOL, V157, P5512
[26]  
HUETTNER C, 1995, AM J PATHOL, V146, P317
[27]   NONPARAMETRIC-ESTIMATION FROM INCOMPLETE OBSERVATIONS [J].
KAPLAN, EL ;
MEIER, P .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1958, 53 (282) :457-481
[28]  
Khuri FR, 2001, CLIN CANCER RES, V7, P861
[29]  
KIM J, 1995, J IMMUNOL, V155, P2240
[30]   A WHOLE-BLOOD TECHNIQUE FOR TESTING PRODUCTION OF HUMAN INTERFERON BY LEUKOCYTES [J].
KIRCHNER, H ;
KLEINICKE, C ;
DIGEL, W .
JOURNAL OF IMMUNOLOGICAL METHODS, 1982, 48 (02) :213-219