Hide or defend, the two strategies of lymphoma immune evasion: potential implications for immunotherapy

被引:79
作者
de Charette, Marie [1 ]
Houot, Roch [1 ,2 ]
机构
[1] CHU Rennes, Serv Hematol Clin, F-35033 Rennes, France
[2] INSERM, U1236, F-35043 Rennes, France
关键词
B-CELL LYMPHOMA; NON-HODGKIN-LYMPHOMA; CLASS-II EXPRESSION; TUMOR-ASSOCIATED MACROPHAGES; FAS LIGAND EXPRESSION; INDEPENDENT PROGNOSTIC-FACTOR; PROGRESSION-FREE SURVIVAL; ANTIGEN-G MOLECULES; REGULATORY T-CELLS; FOLLICULAR LYMPHOMA;
D O I
10.3324/haematol.2017.184192
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Evading immune eradication is a prerequisite for neoplastic progression and one of the hallmarks of cancer. Here, we review the different immune escape strategies of lymphoma and classify them into two main mechanisms. First, lymphoma cells may "hide" to become invisible to the immune system. This can be achieved by losing or down-regulating MHC and/or molecules involved in antigen presentation (including antigen processing machinery and adhesion molecules), thereby preventing their recognition by the immune system. Second, lymphoma cells may "defend" themselves to become resistant to immune eradication. This can be achieved in several ways: by becoming resistant to apoptosis, by expressing inhibitory ligands that deactivate immune cells and/or by inducing an immunosuppressive (humoral and cellular) microenvironment. These immune escape mechanisms may have therapeutic implications. Their identification may be used to guide "personalized immunotherapy" for lymphoma.
引用
收藏
页码:1256 / 1268
页数:13
相关论文
共 182 条
[1]   Fas ligand-mediated immune surveillance by T cells is essential for the control of spontaneous B cell lymphomas [J].
Afshar-Sterle, Shoukat ;
Zotos, Dimitra ;
Bernard, Nicholas J. ;
Scherger, Anna K. ;
Roedling, Lisa ;
Alsop, Amber E. ;
Walker, Jennifer ;
Masson, Frederick ;
Belz, Gabrielle T. ;
Corcoran, Lynn M. ;
O'Reilly, Lorraine A. ;
Strasser, Andreas ;
Smyth, Mark J. ;
Johnstone, Ricky ;
Tarlinton, David M. ;
Nutt, Stephen L. ;
Kallies, Axel .
NATURE MEDICINE, 2014, 20 (03) :283-290
[2]   Prognostic significance of MYC, BCL2, and BCL6 rearrangements in patients with diffuse large B-cell lymphoma treated with cyclophosphamide, doxorubicin, vincristine, and prednisone plus rituximab [J].
Akyurek, Nalan ;
Uner, Aysegul ;
Benekli, Mustafa ;
Barista, Ibrahim .
CANCER, 2012, 118 (17) :4173-4183
[3]  
[Anonymous], ANN REV IMMUNOL
[4]  
[Anonymous], BLOOD ABSTR
[5]  
[Anonymous], ADV IMMUNOLOGY
[6]  
[Anonymous], SEMIN CANC BIOL
[7]  
[Anonymous], EUR J CANC
[8]  
[Anonymous], INT J CANC
[9]   Low Expression of the CIITA Gene Predicts Poor Outcome in Diffuse Large B-Cell Lymphoma [J].
Autio, Matias ;
Jantti, Kirsi ;
Cervera, Alejandra ;
Hautaniemi, Sampsa ;
Leppa, Sirpa .
BLOOD, 2016, 128 (22)
[10]   T-cell defect in diffuse large B-cell lymphomas involves expansion of myeloid-derived suppressor cells [J].
Azzaoui, Imane ;
Uhel, Fabrice ;
Rossille, Delphine ;
Pangault, Celine ;
Dulong, Joelle ;
Le Priol, Jerome ;
Lamy, Thierry ;
Houot, Roch ;
Le Gouill, Steven ;
Cartron, Guillaume ;
Godmer, Pascal ;
Bouabdallah, Krimo ;
Milpied, Noel ;
Damaj, Gandhi ;
Tarte, Karin ;
Fest, Thierry ;
Roussel, Mikael .
BLOOD, 2016, 128 (08) :1081-1092