Anti-PD-1 monoclonal antibody Cancer immunotherapy

被引:0
作者
da Silva, R. Moreira
机构
关键词
Tumor immunity; Melanoma; Renal cell cancer; Non-small cell lung cancer; Nivolumab; BMS-936558; T-CELL-ACTIVATION; PROGRAMMED DEATH-1; PD-1; EXPRESSION; BLOCKADE; LIGANDS; ANTIGEN; SAFETY; B7-H1; AUTOIMMUNITY; REGRESSION;
D O I
10.1358/dof.2014.39.1.2103754
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Mechanistic studies to understand how immune checkpoint blockade induces regressions in several types of cancer have identified therapies that enhance tumor immunity as a treatment strategy. The programmed cell death protein 1 (hPD-1) receptor is a co-inhibitory receptor expressed by activated T lymphocytes. Anti-hPD-1 and anti-programmed cell death 1 ligand 1 (PD-L1) antibodies potentiate immune responses by blocking the interaction between the PD-1 protein and one of its ligands (PD-L), thereby preventing activated cells from becoming anergic, while preserving antitumor immunological activity. Nivolumab, a fully human IgG(4) antibody that blocks this receptor, has been demonstrated to produce durable objective responses, particularly in patients with melanoma, renal cell cancer and non-small cell lung cancer, while exhibiting a better safety profile compared with similar agents acting upon other checkpoint receptors. Herewith, we review all available evidence to illustrate nivolumab's immunological mechanism of action, its pharmacokinetic/pharmacodynamic and safety profile, and preclinical and clinical trials to date with nivolumab alone or combined with other immunomodulators/chemotherapeutics.
引用
收藏
页码:15 / 24
页数:10
相关论文
共 70 条
[1]   Expression of the PD-1 antigen on the surface of stimulated mouse T and B lymphocytes [J].
Agata, Y ;
Kawasaki, A ;
Nishimura, H ;
Ishida, Y ;
Tsubata, T ;
Yagita, H ;
Honjo, T .
INTERNATIONAL IMMUNOLOGY, 1996, 8 (05) :765-772
[2]  
Agrawal S., 2012, 48 ANN M AM SOC CLIN
[3]  
Amin A., 2013, 49 ANN M AM SOC CLIN
[4]  
[Anonymous], 2011, NCC CLIN PRACT GUID
[5]  
[Anonymous], GEN CANC S ORL US FE
[6]  
[Anonymous], 2012, NCCN Clinical Practice Guidelines in Oncology: Breast Cancer
[7]  
[Anonymous], NCCN CLIN PRACT GUID
[8]   Autoimmunity correlates with tumor regression in patients with metastatic melanoma treated with anti-cytotoxic T-lymphocyte antigen-4 [J].
Attia, P ;
Phan, GQ ;
Maker, AV ;
Robinson, MR ;
Quezado, MM ;
Yang, JC ;
Sherry, RM ;
Topalian, SL ;
Kammula, US ;
Royal, RE ;
Restifo, NP ;
Haworth, LR ;
Levy, C ;
Mavroukakis, SA ;
Nichol, G ;
Yellin, MJ ;
Rosenberg, SA .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (25) :6043-6053
[9]   Final Version of 2009 AJCC Melanoma Staging and Classification [J].
Balch, Charles M. ;
Gershenwald, Jeffrey E. ;
Soong, Seng-jaw ;
Thompson, John F. ;
Atkins, Michael B. ;
Byrd, David R. ;
Buzaid, Antonio C. ;
Cochran, Alistair J. ;
Coit, Daniel G. ;
Ding, Shouluan ;
Eggermont, Alexander M. ;
Flaherty, Keith T. ;
Gimotty, Phyllis A. ;
Kirkwood, John M. ;
McMasters, Kelly M. ;
Mihm, Martin C., Jr. ;
Morton, Donald L. ;
Ross, Merrick I. ;
Sober, Arthur J. ;
Sondak, Vernon K. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (36) :6199-6206
[10]   Restoring function in exhausted CD8 T cells during chronic viral infection [J].
Barber, DL ;
Wherry, EJ ;
Masopust, D ;
Zhu, BG ;
Allison, JP ;
Sharpe, AH ;
Freeman, GJ ;
Ahmed, R .
NATURE, 2006, 439 (7077) :682-687