What's the place of immunotherapy in malignant mesothelioma treatments?

被引:28
作者
Gregoire, Marc [1 ]
机构
[1] Res Ctr Oncol Nantes Angers, INSERM, U892, Nantes, France
关键词
mesothelioma; immunotherapy; immune response; cancer virotherapy; chemo-immunotherapy;
D O I
10.4161/cam.4.1.11361
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Malignant pleural mesothelioma (MPM) is a rare malignancy of the pleura with a very poor prognosis. Treatments evaluated for malignant mesothelioma, including chemotherapy, radiotherapy and surgery are of limited efficacy. However, the fact that the tumors of some patients with MPM regress spontaneously or respond to immunotherapy suggests that the immune system may respond to MPM under some circumstances. In this respect, animal studies have demonstrated immunoreactivity of MPM to different immunotherapies. In the case of MPM, several clinical studies have demonstrated a correlation between the presence of a lymphocyte infiltrate and a better prognosis and humoral response directed against specific antigens related to tumor. Thus, MPM immunotherapy is undoubtedly a highly promising but also very challenging approach to the treatment of this disease that has slipped through the defense lines of the immune system. This article reviews past and recent developments of the clinical strategies that concern immunotherapy of mesothelioma.
引用
收藏
页码:153 / 161
页数:9
相关论文
共 103 条
[1]   Imaging and therapy of malignant pleural mesothelioma using replication-competent herpes simplex viruses [J].
Adusumilli, Prasad S. ;
Stiles, Brendon M. ;
Chan, Mei-Ki ;
Mullerad, Michael ;
Eisenberg, David P. ;
Ben-Porat, Leah ;
Huq, Rumana ;
Rusch, Valerie W. ;
Fong, Yuman .
JOURNAL OF GENE MEDICINE, 2006, 8 (05) :603-615
[2]   Cisplatin-induced GADD34 upregulation potentiates oncolytic viral therapy in the treatment of malignant pleural mesothelioma [J].
Adusumilli, PS ;
Chan, MK ;
Chun, YS ;
Hezel, M ;
Chou, TC ;
Rusch, VW ;
Fong, YM .
CANCER BIOLOGY & THERAPY, 2006, 5 (01) :48-53
[3]   IL-2 administration increases CD4+CD25hi Foxp3+ regulatory T cells in cancer patients [J].
Ahmadzadeh, M ;
Rosenberg, ST .
BLOOD, 2006, 107 (06) :2409-2414
[4]   Gene therapy for lung cancer and mesothelioma [J].
Albelda, SM .
CHEST, 1997, 111 (06) :S144-S149
[5]   The interaction between HMGB1 and TLR4 dictates the outcome of anticancer chemotherapy and radiotherapy [J].
Apetoh, Lionel ;
Ghiringhelli, Francois ;
Tesniere, Antoine ;
Criollo, Alfredo ;
Ortiz, Carla ;
Lidereau, Rosette ;
Mariette, Christophe ;
Chaput, Nathalie ;
Mira, Jean-Paul ;
Delaloge, Suzette ;
Andre, Fabrice ;
Tursz, Thomas ;
Kroemer, Guido ;
Zitvogel, Laurence .
IMMUNOLOGICAL REVIEWS, 2007, 220 :47-59
[6]   Characterization of effusion-infiltrating T cells:: Benign versus malignant effusions [J].
Atanackovic, D ;
Block, A ;
de Weerth, A ;
Faltz, C ;
Hossfeld, DK ;
Hegewisch-Becker, S .
CLINICAL CANCER RESEARCH, 2004, 10 (08) :2600-2608
[7]   Toll-like receptors, transduction-effector pathways, and disease diversity: Evidence of an immunobiological paradigm explaining all human illness? [J].
Atkinson, Timothy J. .
INTERNATIONAL REVIEWS OF IMMUNOLOGY, 2008, 27 (04) :255-281
[8]  
Boisgerault N, 2010, IMMUNOTHERA IN PRESS
[9]   Interleukin-12 induces an effective antitumor response in malignant mesothelioma [J].
Caminschi, I ;
Venetsanakos, E ;
Leong, CC ;
Garlepp, MJ ;
Scott, B ;
Robinson, BWS .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1998, 19 (05) :738-746
[10]   Evolving aspects of mesothelioma carcinogenesis: SV40 and genetic predisposition [J].
Carbone, Michele ;
Pass, Harvey I. .
JOURNAL OF THORACIC ONCOLOGY, 2006, 1 (02) :169-171