27
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Trial watch: Peptide-based vaccines in anticancer therapy

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          ABSTRACT

          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

          Related collections

          Most cited references203

          • Record: found
          • Abstract: found
          • Article: not found

          The blockade of immune checkpoints in cancer immunotherapy.

          Among the most promising approaches to activating therapeutic antitumour immunity is the blockade of immune checkpoints. Immune checkpoints refer to a plethora of inhibitory pathways hardwired into the immune system that are crucial for maintaining self-tolerance and modulating the duration and amplitude of physiological immune responses in peripheral tissues in order to minimize collateral tissue damage. It is now clear that tumours co-opt certain immune-checkpoint pathways as a major mechanism of immune resistance, particularly against T cells that are specific for tumour antigens. Because many of the immune checkpoints are initiated by ligand-receptor interactions, they can be readily blocked by antibodies or modulated by recombinant forms of ligands or receptors. Cytotoxic T-lymphocyte-associated antigen 4 (CTLA4) antibodies were the first of this class of immunotherapeutics to achieve US Food and Drug Administration (FDA) approval. Preliminary clinical findings with blockers of additional immune-checkpoint proteins, such as programmed cell death protein 1 (PD1), indicate broad and diverse opportunities to enhance antitumour immunity with the potential to produce durable clinical responses.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Cancer immunotherapy: moving beyond current vaccines.

            Great progress has been made in the field of tumor immunology in the past decade, but optimism about the clinical application of currently available cancer vaccine approaches is based more on surrogate endpoints than on clinical tumor regression. In our cancer vaccine trials of 440 patients, the objective response rate was low (2.6%), and comparable to the results obtained by others. We consider here results in cancer vaccine trials and highlight alternate strategies that mediate cancer regression in preclinical and clinical models.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Immunological aspects of cancer chemotherapy.

              Accumulating evidence indicates that the innate and adaptive immune systems make a crucial contribution to the antitumour effects of conventional chemotherapy-based and radiotherapy-based cancer treatments. Moreover, the molecular and cellular bases of the immunogenicity of cell death that is induced by cytotoxic agents are being progressively unravelled, challenging the guidelines that currently govern the development of anticancer drugs. Here, we review the immunological aspects of conventional cancer treatments and propose that future successes in the fight against cancer will rely on the development and clinical application of combined chemo- and immunotherapies.
                Bookmark

                Author and article information

                Journal
                Oncoimmunology
                Oncoimmunology
                KONI
                koni20
                Oncoimmunology
                Taylor & Francis
                2162-4011
                2162-402X
                2018
                6 September 2018
                6 September 2018
                : 7
                : 12
                : e1511506
                Affiliations
                [a ]Faculty of Medicine, University of Paris Sud/Paris XI , Le Kremlin-Bicêtre, France
                [b ]Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus , Villejuif, France
                [c ]Equipe 11 labellisée Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers ,Paris, France
                [d ]U1138, INSERM , Paris, France
                [e ]Université Paris Descartes/Paris V , Paris, France
                [f ]Université Pierre et Marie Curie/Paris VI , Paris, France
                [g ]Sotio , Prague, Czech Republic
                [h ]Dept. of Immunology, 2nd Faculty of Medicine and University Hospital Motol, Charles University , Prague, Czech Republic
                [i ]Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 1428 , Villejuif, France
                [j ]INSERM, U1015, Gustave Roussy Cancer Campus , Villejuif, France
                [k ]Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP , Paris, France
                [l ]Department of Women’s and Children’s Health, Karolinska University Hospital , Stockholm, Sweden
                [m ]Department of Radiation Oncology, Weill Cornell Medical College , New York, NY, USA
                [n ]Sandra and Edward Meyer Cancer Center , New York, NY, USA
                Author notes
                CONTACT Lorenzo Galluzzi deadoc@ 123456vodafone.it Weill Cornell Medical College, Department of Radiation Oncology , 525 East 68th Street, Box # 169, New York, NY 10065, USA
                Author information
                http://orcid.org/0000-0002-3569-6066
                http://orcid.org/0000-0002-6081-9558
                http://orcid.org/0000-0002-9334-4405
                Article
                1511506
                10.1080/2162402X.2018.1511506
                6279318
                30524907
                9b6e2f2e-e2c1-4a85-ba62-4e703dc0de78
                © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC.

                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.

                History
                : 10 August 2018
                Page count
                Tables: 1, References: 275, Pages: 15
                Categories
                Review

                Immunology
                car t cells,immune checkpoint blockers,magea3,mutational load,ny-eso-1,synthetic long peptides,tumor neoantigens

                Comments

                Comment on this article