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Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)

The interface between malignant melanoma and patient immunity has long been recognised and efforts to treat this most lethal form of skin cancer by activating immune responses with cytokine, vaccine and also antibody immunotherapies have demonstrated promise in limited subsets of patients. In the pr...

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Autores principales: MALAS, SADEK, HARRASSER, MICAELA, LACY, KATIE E., KARAGIANNIS, SOPHIA N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121424/
https://www.ncbi.nlm.nih.gov/pubmed/24969320
http://dx.doi.org/10.3892/or.2014.3275
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author MALAS, SADEK
HARRASSER, MICAELA
LACY, KATIE E.
KARAGIANNIS, SOPHIA N.
author_facet MALAS, SADEK
HARRASSER, MICAELA
LACY, KATIE E.
KARAGIANNIS, SOPHIA N.
author_sort MALAS, SADEK
collection PubMed
description The interface between malignant melanoma and patient immunity has long been recognised and efforts to treat this most lethal form of skin cancer by activating immune responses with cytokine, vaccine and also antibody immunotherapies have demonstrated promise in limited subsets of patients. In the present study, we discuss different antibody immunotherapy approaches evaluated in the context of melanoma, each designed to act on distinct targets and to employ different mechanisms to restrict tumour growth and spread. Monoclonal antibodies recognising melanoma-associated antigens such as CSPG4/MCSP and targeting elements of tumour-associated vasculature (VEGF) have constituted long-standing translational approaches aimed at reducing melanoma growth and metastasis. Recent insights into mechanisms of immune regulation and tumour-immune cell interactions have helped to identify checkpoint molecules on immune (CTLA4, PD-1) and tumour (PD-L1) cells as promising therapeutic targets. Checkpoint blockade with antibodies to activate immune responses and perhaps to counteract melanoma-associated immunomodulatory mechanisms led to the first clinical breakthrough in the form of an anti-CTLA4 monoclonal antibody. Novel modalities to target key mechanisms of immune suppression and to redirect potent effector cell subsets against tumours are expected to improve clinical outcomes and to provide previously unexplored avenues for therapeutic interventions.
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spelling pubmed-41214242014-08-12 Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review) MALAS, SADEK HARRASSER, MICAELA LACY, KATIE E. KARAGIANNIS, SOPHIA N. Oncol Rep Articles The interface between malignant melanoma and patient immunity has long been recognised and efforts to treat this most lethal form of skin cancer by activating immune responses with cytokine, vaccine and also antibody immunotherapies have demonstrated promise in limited subsets of patients. In the present study, we discuss different antibody immunotherapy approaches evaluated in the context of melanoma, each designed to act on distinct targets and to employ different mechanisms to restrict tumour growth and spread. Monoclonal antibodies recognising melanoma-associated antigens such as CSPG4/MCSP and targeting elements of tumour-associated vasculature (VEGF) have constituted long-standing translational approaches aimed at reducing melanoma growth and metastasis. Recent insights into mechanisms of immune regulation and tumour-immune cell interactions have helped to identify checkpoint molecules on immune (CTLA4, PD-1) and tumour (PD-L1) cells as promising therapeutic targets. Checkpoint blockade with antibodies to activate immune responses and perhaps to counteract melanoma-associated immunomodulatory mechanisms led to the first clinical breakthrough in the form of an anti-CTLA4 monoclonal antibody. Novel modalities to target key mechanisms of immune suppression and to redirect potent effector cell subsets against tumours are expected to improve clinical outcomes and to provide previously unexplored avenues for therapeutic interventions. D.A. Spandidos 2014-09 2014-06-20 /pmc/articles/PMC4121424/ /pubmed/24969320 http://dx.doi.org/10.3892/or.2014.3275 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
MALAS, SADEK
HARRASSER, MICAELA
LACY, KATIE E.
KARAGIANNIS, SOPHIA N.
Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title_full Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title_fullStr Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title_full_unstemmed Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title_short Antibody therapies for melanoma: New and emerging opportunities to activate immunity (Review)
title_sort antibody therapies for melanoma: new and emerging opportunities to activate immunity (review)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4121424/
https://www.ncbi.nlm.nih.gov/pubmed/24969320
http://dx.doi.org/10.3892/or.2014.3275
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