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Trial watch: Peptide-based vaccines in anticancer therapy

Peptide-based anticancer vaccination aims at stimulating an immune response against one or multiple tumor-associated antigens (TAAs) following immunization with purified, recombinant or synthetically engineered epitopes. Despite high expectations, the peptide-based vaccines that have been explored i...

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Autores principales: Bezu, Lucillia, Kepp, Oliver, Cerrato, Giulia, Pol, Jonathan, Fucikova, Jitka, Spisek, Radek, Zitvogel, Laurence, Kroemer, Guido, Galluzzi, Lorenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279318/
https://www.ncbi.nlm.nih.gov/pubmed/30524907
http://dx.doi.org/10.1080/2162402X.2018.1511506
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author Bezu, Lucillia
Kepp, Oliver
Cerrato, Giulia
Pol, Jonathan
Fucikova, Jitka
Spisek, Radek
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
author_facet Bezu, Lucillia
Kepp, Oliver
Cerrato, Giulia
Pol, Jonathan
Fucikova, Jitka
Spisek, Radek
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
author_sort Bezu, Lucillia
collection PubMed
description Peptide-based anticancer vaccination aims at stimulating an immune response against one or multiple tumor-associated antigens (TAAs) following immunization with purified, recombinant or synthetically engineered epitopes. Despite high expectations, the peptide-based vaccines that have been explored in the clinic so far had limited therapeutic activity, largely due to cancer cell-intrinsic alterations that minimize antigenicity and/or changes in the tumor microenvironment that foster immunosuppression. Several strategies have been developed to overcome such limitations, including the use of immunostimulatory adjuvants, the co-treatment with cytotoxic anticancer therapies that enable the coordinated release of damage-associated molecular patterns, and the concomitant blockade of immune checkpoints. Personalized peptide-based vaccines are also being explored for therapeutic activity in the clinic. Here, we review recent preclinical and clinical progress in the use of peptide-based vaccines as anticancer therapeutics.Abbreviations: CMP: carbohydrate-mimetic peptide; CMV: cytomegalovirus; DC: dendritic cell; FDA: Food and Drug Administration; HPV: human papillomavirus; MDS: myelodysplastic syndrome; MHP: melanoma helper vaccine; NSCLC: non-small cell lung carcinoma; ODD: orphan drug designation; PPV: personalized peptide vaccination; SLP: synthetic long peptide; TAA: tumor-associated antigen; TNA: tumor neoantigen
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spelling pubmed-62793182018-12-06 Trial watch: Peptide-based vaccines in anticancer therapy Bezu, Lucillia Kepp, Oliver Cerrato, Giulia Pol, Jonathan Fucikova, Jitka Spisek, Radek Zitvogel, Laurence Kroemer, Guido Galluzzi, Lorenzo Oncoimmunology Review Peptide-based anticancer vaccination aims at stimulating an immune response against one or multiple tumor-associated antigens (TAAs) following immunization with purified, recombinant or synthetically engineered epitopes. Despite high expectations, the peptide-based vaccines that have been explored in the clinic so far had limited therapeutic activity, largely due to cancer cell-intrinsic alterations that minimize antigenicity and/or changes in the tumor microenvironment that foster immunosuppression. Several strategies have been developed to overcome such limitations, including the use of immunostimulatory adjuvants, the co-treatment with cytotoxic anticancer therapies that enable the coordinated release of damage-associated molecular patterns, and the concomitant blockade of immune checkpoints. Personalized peptide-based vaccines are also being explored for therapeutic activity in the clinic. Here, we review recent preclinical and clinical progress in the use of peptide-based vaccines as anticancer therapeutics.Abbreviations: CMP: carbohydrate-mimetic peptide; CMV: cytomegalovirus; DC: dendritic cell; FDA: Food and Drug Administration; HPV: human papillomavirus; MDS: myelodysplastic syndrome; MHP: melanoma helper vaccine; NSCLC: non-small cell lung carcinoma; ODD: orphan drug designation; PPV: personalized peptide vaccination; SLP: synthetic long peptide; TAA: tumor-associated antigen; TNA: tumor neoantigen Taylor & Francis 2018-09-06 /pmc/articles/PMC6279318/ /pubmed/30524907 http://dx.doi.org/10.1080/2162402X.2018.1511506 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Review
Bezu, Lucillia
Kepp, Oliver
Cerrato, Giulia
Pol, Jonathan
Fucikova, Jitka
Spisek, Radek
Zitvogel, Laurence
Kroemer, Guido
Galluzzi, Lorenzo
Trial watch: Peptide-based vaccines in anticancer therapy
title Trial watch: Peptide-based vaccines in anticancer therapy
title_full Trial watch: Peptide-based vaccines in anticancer therapy
title_fullStr Trial watch: Peptide-based vaccines in anticancer therapy
title_full_unstemmed Trial watch: Peptide-based vaccines in anticancer therapy
title_short Trial watch: Peptide-based vaccines in anticancer therapy
title_sort trial watch: peptide-based vaccines in anticancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279318/
https://www.ncbi.nlm.nih.gov/pubmed/30524907
http://dx.doi.org/10.1080/2162402X.2018.1511506
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