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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2018
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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 |
format | Online Article Text |
id | pubmed-6279318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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