Anti-Cancer immunotherapy: Immunomodulating agents in clinical development

被引:0
|
作者
Loirat, D. [1 ,2 ,3 ]
Le Tourneau, C. [1 ,2 ,4 ]
机构
[1] Inst Curie, Dept Med Oncol, F-75005 Paris, France
[2] Inst Curie, Dept Med Oncol, F-92210 St Cloud, France
[3] Inst Curie, Translat Immunotherapy Team, Inserm U932, Dept Transferts, F-75005 Paris, France
[4] Inst Curie, Inserm U900, F-75005 Paris, France
关键词
Immunotherapy; Immune checkpoint; Clinical trials; Cancer; CELL LUNG-CANCER; 9 AGONIST IMO-2055; ADVANCED MELANOMA; ANTI-PD-L1; ANTIBODY; UNTREATED MELANOMA; ANTITUMOR-ACTIVITY; PHASE-3; TRIAL; SOLID TUMORS; DOUBLE-BLIND; IPILIMUMAB;
D O I
10.1007/s10269-015-2546-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immune response often fails to control tumor development due to the activation of inefficient lymphocyte or tolerization mechanisms. The goal of immunotherapeutics is to reverse the balance between the immune response and tumor growth. Targeting immune checkpoints involved in the activation or inhibition pathways of specific immune response is an emerging strategy. It has shown promising results for metastatic melanoma with antibodies targeting CTLA4, and more recently with antibodies targeting PD- 1/PD-L1 in melanoma and also other types of tumor. Therapies targeting B7 family members (CTLA4, PD-1, PD-L1/2, etc.) are the most advanced in clinical development, but molecules belonging to TNF-R family (OX40, CD40, GITR, CD137, etc.) also appear to be promising. In this article, we present a review of the different pathways involved in immune response modulation and corresponding therapeutic agents under clinical development.
引用
收藏
页码:379 / 389
页数:11
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