Analysis of the natural killer mediated immune response in metastatic renal cell carcinoma patients

被引:28
作者
Gati, A
Da Rocha, S
Guerra, N
Escudier, B
Moretta, A
Chouaib, S
Angevin, E
Caignard, A
机构
[1] Inst Gustave Roussy, INSERM, U 487 Cytokines & Immunite Antitumorale, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Unite Therapies Innovantes, Villejuif, France
[3] Univ Genoa, Dipartimento Med Sperimentale, Genoa, Italy
关键词
renal tumors; immune response; NK cells; immunotherapy;
D O I
10.1002/ijc.11730
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastatic renal cell carcinomas (MRCC) are considered as immunogeneic tumors on the basis of the clinical responses observed in patients treated by IL-2. However, renal cell carcinoma patients are also characterized by alterations of the immune response that may compromise the immunotherapeutic approaches. In our study, we have studied the phenotype and the functional capacities of peripheral NK cells in a panel of neprectomized metastatic renal cell carcinoma patients. NK cells were harvested by negative immunoselection from fresh peripheral blood samples. In most of MRCC patients analysed (23/28), the expression of NCR (NKp46 and NKp30) was similar to that of donors. Lytic capacities by activated immunoselected NK cells from MRCC patients assessed against K562 and 3 renal tumor cell lines were in the range of that observed in NK cells from normal donors. HLA-I- renal tumor cells UOK23 were killed with a good efficiency, whereas HLA-I renal tumor cells were more resistant. Although LFA-1/ICAM-1 interaction potentiates RCC cell lysis, HLA-I/NKR interaction clearly decreased RCC cell susceptibility to NK cells. In addition, proliferation of NK cells from MRCC patients in response to cytokines was altered. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:393 / 401
页数:9
相关论文
共 33 条
[1]  
ANGLARD P, 1992, CANCER RES, V52, P348
[2]   Leukemic target susceptibility to natural killer cytotoxicity: relationship with BCR-ABL expression [J].
Baron, F ;
Turhan, AG ;
Giron-Michel, J ;
Azzarone, B ;
Bentires-Alj, M ;
Bours, V ;
Bourhis, JH ;
Chouaib, S ;
Caignard, A .
BLOOD, 2002, 99 (06) :2107-2113
[3]   Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire [J].
Campbell, JJ ;
Qin, SX ;
Unutmaz, D ;
Soler, D ;
Murphy, KE ;
Hodge, MR ;
Wu, LJ ;
Butcher, EC .
JOURNAL OF IMMUNOLOGY, 2001, 166 (11) :6477-6482
[4]  
Carayol G, 1998, EUR J IMMUNOL, V28, P1991, DOI 10.1002/(SICI)1521-4141(199806)28:06<1991::AID-IMMU1991>3.0.CO
[5]  
2-7
[6]   Altered natural killer cell differentiation in CD34+ progenitors from chronic myeloid leukemia patients [J].
Carayol, G ;
Giron-Michel, J ;
Azzarone, B ;
Castagna, L ;
Cambier, N ;
Mishal, Z ;
Bourhis, JH ;
Chouaib, S ;
Caignard, A .
ONCOGENE, 2000, 19 (23) :2758-2766
[7]   Transforming growth factor β1 inhibits expression of NKp30 and NKG2D receptors:: Consequences for the NK-mediated killing of dendritic cells [J].
Castriconi, R ;
Cantoni, C ;
Della Chiesa, M ;
Vitale, M ;
Marcenaro, E ;
Conte, R ;
Biassoni, R ;
Bottino, C ;
Moretta, L ;
Moretta, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :4120-4125
[8]  
Childs RW, 2001, CRIT REV IMMUNOL, V21, P191
[9]   Human natural killer cells:: a unique innate immunoregulatory role for the CD56bright subset [J].
Cooper, MA ;
Fehniger, TA ;
Turner, SC ;
Chen, KS ;
Ghaheri, BA ;
Ghayur, T ;
Carson, WE ;
Caligiuri, MA .
BLOOD, 2001, 97 (10) :3146-3151
[10]  
Cosman D, 2001, IMMUNITY, V14, P123, DOI 10.1016/S1074-7613(01)00095-4