Gamma-delta T-cells in patients with squamous cell carcinoma of the head and neck

被引:24
作者
Bas, Murat
Bier, Henning
Schirlau, Kerstin
Friebe-Hoffmann, Ulrike
Scheckenbach, Kathrin
Balz, Vera
Whiteside, Theresa L.
Hoffmann, Thomas K.
机构
[1] Univ Dusseldorf, Dept Otorhinolaryngol, D-40225 Dusseldorf, Germany
[2] Univ Dusseldorf, Dept Obstet & Gynecol, D-40225 Dusseldorf, Germany
[3] Univ Pittsburgh, Hillman Canc Ctr, Pittsburgh, PA USA
关键词
gamma-delta T-cells; cancer immunology; squamous cell carcinoma of the head and neck;
D O I
10.1016/j.oraloncology.2005.11.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In our attempt to characterize a general immune-suppression found in patients with squamous cell carcinoma of the head and neck (SCCHN) we now focused on a subset of CD3 lymphocytes described as gamma/delta-T-celts, a cell type with potential relevance in non-MHC restricted anti-tumor immune responses. Peripheral blood of 33 SCCHN patients and 33 age-matched controls (CON) was evaluated for the frequency of gamma/delta-T-cells among CD3(+) T-cells and their onset of apoptosis (Annexin V binding) by multicolor flow cytometry. Results were correlated with clinical parameters. Patients with SCCHN had a significantly higher proportion of gamma/delta-T-cells compared to healthy controls (4.4 +/- 0.4% for SCCHN vs. 3.0 +/- 0.3% for CON, p = 0.01). However, this increase was not paralleled with a difference in the onset of apoptosis if compared to CON. There was also no correlation between the proportion of gamma/delta-T-cells and tumor stage. However, a significantly higher proportion of gamma/delta-T-cells was found in patients with recurrent or metachronous second primary SCCHN (6.0 +/- 1.0%) if compared to the other SCCHN (3.8 +/- 0.4%, p = 0.02). In a follow up 3-6 months post-treatment patients showed a decrease of gamma/delta-T-cells among CD3(+) cells (2.7 +/- 0.4%, n = 4) if they were operated only and an increase if primary radio-chemotherapy (6.7 +/- 1.7%, n = 8) or a combination of operation plus radio-chemotherapy (6.8 +/- 2.3%, n = 3) was applied. Furthermore, patients receiving palliative treatment including radio-chemotherapy had highest values Of gamma/delta-T-cells (9.1 +/- 2.7%, n = 4) overall implicating that the treatment modality significantly influences the proportion Of gamma/delta-T-cells. Since patients with SCCHN, particularly those with recurrent or second primary disease after treatment, had a higher proportion of gamma/delta-T-cells without signs of a reduced onset of apoptosis this could be due to an increased de novo generation. The current study implies that increased frequencies of gamma/delta-T-cells in patients with SCCHN may not only be the result of tumor-host interactions but the consequence of applied treatment modalities. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:691 / 697
页数:7
相关论文
共 30 条
[1]   Reduced number and impaired function of circulating γδ T cells in patients with cutaneous primary melanoma [J].
Argentati, K ;
Re, F ;
Serresi, S ;
Tucci, MG ;
Bartozzi, B ;
Bernardini, G ;
Provinciali, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (05) :829-834
[2]   A FUNCTIONAL T3 MOLECULE ASSOCIATED WITH A NOVEL HETERODIMER ON THE SURFACE OF IMMATURE HUMAN THYMOCYTES [J].
BANK, I ;
DEPINHO, RA ;
BRENNER, MB ;
CASSIMERIS, J ;
ALT, FW ;
CHESS, L .
NATURE, 1986, 322 (6075) :179-181
[3]   2 FORMS OF THE T-CELL RECEPTOR GAMMA-PROTEIN FOUND ON PERIPHERAL-BLOOD CYTOTOXIC T-LYMPHOCYTES [J].
BRENNER, MB ;
MCLEAN, J ;
SCHEFT, H ;
RIBERDY, J ;
ANG, SL ;
SEIDMAN, JG ;
DEVLIN, P ;
KRANGEL, MS .
NATURE, 1987, 325 (6106) :689-694
[4]   COMPARISON OF CYTOLYTIC AND PROLIFERATIVE ACTIVITIES OF HUMAN-GAMMA-DELTA AND ALPHA-BETA-T-CELLS FROM PERIPHERAL-BLOOD AGAINST VARIOUS HUMAN TUMOR-CELL LINES [J].
ENSSLIN, AS ;
FORMBY, B .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (21) :1564-1569
[5]  
FALINI B, 1989, J IMMUNOL, V143, P2480
[6]   Killing of laminin receptor-positive human lung cancers by tumor-infiltrating lymphocytes bearing gamma delta(+) T-cell receptors [J].
Ferrarini, M ;
Heltai, S ;
Pupa, SM ;
Menard, S ;
Zocchi, MR .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (07) :436-441
[7]   Cisplatin triggers apoptotic or nonapoptotic cell death in Fanconi anemia lymphoblasts in a concentration-dependent manner [J].
Ferrer, M ;
Izeboud, T ;
Ferreira, CG ;
Span, SW ;
Giaccone, G ;
Kruyt, FAE .
EXPERIMENTAL CELL RESEARCH, 2003, 286 (02) :381-395
[8]  
Hoffmann TK, 2002, CLIN CANCER RES, V8, P1787
[9]  
Hoffmann TK, 2002, CLIN CANCER RES, V8, P2553
[10]  
HOFFMANN TK, 2004, CANC IMMUNOL IMMUNOT