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High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies

We tested how to eradicate long-established immunogenic tumors that were resistant to the monoclonal antibody-mediated blockade of PD-L1 (PD-1 ligand 1) and cytotoxic T lymphocyte-associated protein 4 (CTLA4). Bacterial vaccination with a tumor-specific peptide exhibiting a high affinity for its res...

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Detalles Bibliográficos
Autores principales: Binder, David C, Schreiber, Hans
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923789/
https://www.ncbi.nlm.nih.gov/pubmed/24563823
http://dx.doi.org/10.4161/onci.26704
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author Binder, David C
Schreiber, Hans
author_facet Binder, David C
Schreiber, Hans
author_sort Binder, David C
collection PubMed
description We tested how to eradicate long-established immunogenic tumors that were resistant to the monoclonal antibody-mediated blockade of PD-L1 (PD-1 ligand 1) and cytotoxic T lymphocyte-associated protein 4 (CTLA4). Bacterial vaccination with a tumor-specific peptide exhibiting a high affinity for its respective MHC molecule consistently eradicated tumors when combined with a PD-L1 blocking antibody. This approach can be translated to the clinic by combining cancer cell whole-exome sequencing with algorithms to identify mutant peptides with high peptide-MHC binding affinity.
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spelling pubmed-39237892014-02-21 High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies Binder, David C Schreiber, Hans Oncoimmunology Author's View We tested how to eradicate long-established immunogenic tumors that were resistant to the monoclonal antibody-mediated blockade of PD-L1 (PD-1 ligand 1) and cytotoxic T lymphocyte-associated protein 4 (CTLA4). Bacterial vaccination with a tumor-specific peptide exhibiting a high affinity for its respective MHC molecule consistently eradicated tumors when combined with a PD-L1 blocking antibody. This approach can be translated to the clinic by combining cancer cell whole-exome sequencing with algorithms to identify mutant peptides with high peptide-MHC binding affinity. Landes Bioscience 2013-12-01 2013-10-22 /pmc/articles/PMC3923789/ /pubmed/24563823 http://dx.doi.org/10.4161/onci.26704 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/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 Author's View
Binder, David C
Schreiber, Hans
High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title_full High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title_fullStr High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title_full_unstemmed High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title_short High-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
title_sort high-affinity peptide-based anticancer vaccination to overcome resistance to immunostimulatory antibodies
topic Author's View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3923789/
https://www.ncbi.nlm.nih.gov/pubmed/24563823
http://dx.doi.org/10.4161/onci.26704
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