Immunologic mechanisms in RCC and allogeneic renal transplant rejection

被引:12
作者
Bedke, Jens [1 ]
Stenzl, Arnulf [1 ]
机构
[1] Univ Tubingen, Dept Urol, D-72076 Tubingen, Germany
关键词
REGULATORY-T-CELLS; TUMOR-INFILTRATING MACROPHAGES; ANTI-CD28; MONOCLONAL-ANTIBODY; PHASE-III TRIAL; ALLOGRAFT-REJECTION; IN-VITRO; CANCER-IMMUNOTHERAPY; CHEMOKINE RECEPTORS; ANTITUMOR IMMUNITY; DENDRITIC CELLS;
D O I
10.1038/nrurol.2010.59
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The tolerance state that exists between renal cell carcinoma (RCC) and the host's immune system would be an ideal situation in the setting of human kidney transplantation, in which graft tolerance is the ultimate goal of immunosuppressive therapy. On the other hand, acute rejection, as it appears in renal allografts, would be the optimal immunologic situation in patients with RCC. Analysis of the underlying mechanisms of acute allograft rejection and local pro-tumor immunosuppression could help to identify potential therapeutic targets for inducing immune tolerance in allograft recipients and immune rejection in RCC patients. Experimental kidney transplantation might be a suitable model in which to analyze these processes. Macrophages are a prominent and vital cell type in the cellular infiltrate seen in both RCC and renal allografts. Depending on their polarization, they can initiate and promote either proinflammatory or pro-tumor responses, which lead to tissue rejection or acceptance, respectively. Improved understanding of macrophage biology could lead to therapeutic modification of their function in order to promote a desirable immunologic response in either RCC or transplant tissue.
引用
收藏
页码:339 / 347
页数:9
相关论文
共 96 条
[1]  
[Anonymous], DENILEUKIN DIFTITOX
[2]   Cancer and the chemokine network [J].
Balkwill, F .
NATURE REVIEWS CANCER, 2004, 4 (07) :540-550
[3]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[4]   Migration of human monocytes in response to vascular endothelial growth factor (VEGF) is mediated via the VEGF receptor flt-1 [J].
Barleon, B ;
Sozzani, S ;
Zhou, D ;
Weich, HA ;
Mantovani, A ;
Marme, D .
BLOOD, 1996, 87 (08) :3336-3343
[5]   Beneficial effects of CCR1 blockade on the progression of chronic renal allograft damage [J].
Bedke, J. ;
Kiss, E. ;
Schaefer, L. ;
Behnes, C. -L. ;
Bonrouhi, M. ;
Gretz, N. ;
Horuk, R. ;
Diedrichs-Moehring, M. ;
Wildner, G. ;
Nelson, P. J. ;
Groene, H. J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2007, 7 (03) :527-537
[6]   Anti-inflammatory effects of αv integrin antagonism in acute kidney allograft rejection [J].
Bedke, Jens ;
Kiss, Eva ;
Behnes, Carl-Ludwig ;
Popovic, Zoran V. ;
Heuser, Markus ;
Stojanovic, Tomislav ;
Sijmonsma, Tjeerd ;
Huber, Peter ;
Domhan, Sophie ;
Muschal, Stefan ;
Abdollahi, Amir ;
Gretz, Norbert ;
Groene, Hermann-Josef .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 171 (04) :1127-1139
[7]   A novel CXCL8 protein-based antagonist in acute experimental renal allograft damage [J].
Bedke, Jens ;
Nelson, Peter J. ;
Kiss, Eva ;
Muenchmeier, Niklas ;
Rek, Angelika ;
Behnes, Carl-Ludwig ;
Gretz, Norbert ;
Kungl, Andreas J. ;
Groene, Hermann-Josef .
MOLECULAR IMMUNOLOGY, 2010, 47 (05) :1047-1057
[8]   A distinct and unique transcriptional program expressed by tumor-associated macrophages (defective NF-κB and enhanced IRF-3/STAT1 activation) [J].
Biswas, SK ;
Gangi, L ;
Paul, S ;
Schioppa, T ;
Saccani, A ;
Sironi, M ;
Bottazzi, B ;
Doni, A ;
Vincenzo, B ;
Pasqualini, F ;
Vago, L ;
Nebuloni, M ;
Mantovani, A ;
Sica, A .
BLOOD, 2006, 107 (05) :2112-2122
[9]  
Brossart P, 1998, CANCER RES, V58, P732
[10]   ANTITUMOR AND ANTIMETASTATIC ACTIVITY OF INTERLEUKIN-12 AGAINST MURINE TUMORS [J].
BRUNDA, MJ ;
LUISTRO, L ;
WARRIER, RR ;
WRIGHT, RB ;
HUBBARD, BR ;
MURPHY, M ;
WOLF, SF ;
GATELY, MK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (04) :1223-1230