Immunology and Biotherapies
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Page Ressources et Actualités du DIU immunologie et biothérapies
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Rescooped by Gilbert C FAURE from Cancer Vaccines Collection
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Clinical deployment of antibodies for treatment of melanoma

Abstract

The concept of using immunotherapy to treat melanoma has existed for decades. The rationale comes from the knowledge that many patients with melanoma have endogenous immune responses against their tumor cells and clinically meaningful tumor regression can be achieved in a minority of patients using cytokines such as interleukin-2 and adoptive cellular therapy. In the last 5 years there has been a revolution in the clinical management of melanoma in large measure based on the development of antibodies that influence T cell regulatory pathways by overcoming checkpoint inhibition and providing co-stimulation, either of which results in significantly more effective immune-mediated tumor destruction. This review will describe the pre-clinical and clinical application of antagonistic antibodies targeting the T-cell checkpoints cytotoxic T-lymphocyte antigen 4 (CTLA-4) and programmed death 1 (PD-1), and agonistic antibodies targeting the costimulatory pathways OX40 and 4-1BB. Recent progress and opportunities for future investigation of combination antibody therapy will be described.


Via Krishan Maggon
Krishan Maggon 's curator insight, March 9, 2015 3:56 AM

Highlights

 

Melanoma treatment has been transformed using T-cell checkpoint antibodies.

Antibodies to CTLA-4 and PD-1 have had the largest impact on melanoma management.

Combination T-cell checkpoint therapy holds great promise for clinical development.

OX40 and 4-1BB are T cell costimulators with clinical potential in melanoma.

 

 

Rescooped by Gilbert C FAURE from Cancer Immunotherapy Review and Collection
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Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodies

Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodies | Immunology and Biotherapies | Scoop.it
Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodies http://t.co/4XGxIKdg1U #immunotherapy #lungcancer #awareness #LCAM @OxfordJournals

 

Abstract

Despite extensive investigation over the past three decades, cancer immunotherapy has produced limited success, with few agents achieving approval by the Food and Drug Administration and even the most effective helping only a minority of patients, primarily with melanoma or renal cancer. In recent years, immune checkpoints that maintain physiologic self-tolerance have been implicated in the down-regulation of anti-tumor immunity. Efforts to restore latent anti-tumor immunity have focused on antibody-based interventions targeting CTL antigen 4 (CTLA-4) and programmed cell death protein 1 (PD-1) on T lymphocytes and its principal ligand (PD-L1) on tumor cells. Ipilimumab, an antibody targeting CTLA-4, appears to restore tumor immunity at the priming phase, whereas anti-PD-1/PD-L1 antibodies restore immune function in the tumor microenvironment. Although ipilimumab can produce durable long-term responses in patients with advanced melanoma, it is associated with significant immune-related toxicities. By contrast, antibodies targeting either PD-1 or PD-L1 have produced significant anti-tumor activity with considerably less toxicity. Activity was seen in patients with melanoma and renal cancer, as well as those with non-small-cell lung, bladder and head and neck cancers, tumors not previously felt to be sensitive to immunotherapy. The tolerability of PD-1-pathway blockers and their unique mechanism of action have made them ideal backbones for combination regimen development. Combination approaches involving cytotoxic chemotherapy, anti-angiogenic agents, alternative immune-checkpoint inhibitors, immunostimulatory cytokines and cancer vaccines are currently under clinical investigation. Current efforts focus on registration trials of single agents and combinations in various diseases and disease settings and identifying predictive biomarkers of response.

Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodiesTable 1.

Antibodies that target the PD-1 axis and are undergoing clinical investigation for cancer

 TargetAntibodyMolecular structureClinical development phaseTumor types in evaluationPD-1Nivolumab (BMS-936558)Fully human IgG4Phase IIIMelanoma, RCC, NSCLC, HNSCCPembrolizumab (MK-3475)Humanized IgG4Phase IIIMelanoma, NSCLCPidilizumab (CT-011)Humanized IgG1κPhase IIHEME, melanomaPD-L1BMS-936559Fully human IgG4Phase IAdvanced solid tumorsMPDL3280AFully human IgG1Phase IMelanoma, RCC, NSCLCPhase IIUROMEDI4736Fully human IgG1Phase IAdvanced solid tumorsPhase IIINSCLCMSB0010718CFully human IgG1Phase IAdvanced solid tumorsPhase IIMerkel cell carcinoma
Via Krishan Maggon
Krishan Maggon 's curator insight, November 15, 2014 1:38 AM

Review of the current status of active PD1/PDL1 projects                    

 

 

Int. Immunol. (2014)doi: 10.1093/intimm/dxu095                                     First published online: October 16, 2014

 

Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodiesGeorge K. Philips1 and Michael Atkins2

+Author Affiliations

1 Department of Medicine, Georgetown University Hospital, 3800 Reservoir Road NW, Washington DC 20007, USA2 Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Research Building-E501, 3970 Reservoir Road NW, Washington DC 20057, USACorrespondence to: G. K. Philips; E-mail: george.k.philips@gunet.georgetown.eduReceived September 4, 2014.Accepted October 3, 2014.
Krishan Maggon 's curator insight, November 15, 2014 2:06 AM

Review of the current status of active PD1/PDL1 projects                    

 

 

Int. Immunol. (2014)doi: 10.1093/intimm/dxu095                                     First published online: October 16, 2014

 

Therapeutic uses of anti-PD-1 and anti-PD-L1 antibodiesGeorge K. Philips1 and Michael Atkins2

+Author Affiliations

1 Department of Medicine, Georgetown University Hospital, 3800 Reservoir Road NW, Washington DC 20007, USA2 Department of Oncology, Georgetown-Lombardi Comprehensive Cancer Center, Research Building-E501, 3970 Reservoir Road NW, Washington DC 20057, USACorrespondence to: G. K. Philips; E-mail: george.k.philips@gunet.georgetown.eduReceived September 4, 2014.Accepted October 3, 2014.