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      Trial watch: chemotherapy-induced immunogenic cell death in immuno-oncology

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          ABSTRACT

          The term ‘immunogenic cell death’ (ICD) denotes an immunologically unique type of regulated cell death that enables, rather than suppresses, T cell-driven immune responses that are specific for antigens derived from the dying cells. The ability of ICD to elicit adaptive immunity heavily relies on the immunogenicity of dying cells, implying that such cells must encode and present antigens not covered by central tolerance (antigenicity), and deliver immunostimulatory molecules such as damage-associated molecular patterns and cytokines (adjuvanticity). Moreover, the host immune system must be equipped to detect the antigenicity and adjuvanticity of dying cells. As cancer (but not normal) cells express several antigens not covered by central tolerance, they can be driven into ICD by some therapeutic agents, including (but not limited to) chemotherapeutics of the anthracycline family, oxaliplatin and bortezomib, as well as radiation therapy. In this Trial Watch, we describe current trends in the preclinical and clinical development of ICD-eliciting chemotherapy as partner for immunotherapy, with a focus on trials assessing efficacy in the context of immunomonitoring.

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          Most cited references301

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          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.
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            Cell-surface calreticulin initiates clearance of viable or apoptotic cells through trans-activation of LRP on the phagocyte.

            Apoptotic-cell removal is critical for development, tissue homeostasis, and resolution of inflammation. Although many candidate systems exist, only phosphatidylserine has been identified as a general recognition ligand on apoptotic cells. We demonstrate here that calreticulin acts as a second general recognition ligand by binding and activating LDL-receptor-related protein (LRP) on the engulfing cell. Since surface calreticulin is also found on viable cells, a mechanism preventing inadvertent uptake was sought. Disruption of interactions between CD47 (integrin-associated protein) on the target cell and SIRPalpha (SHPS-1), a heavily glycosylated transmembrane protein on the engulfing cell, permitted uptake of viable cells in a calreticulin/LRP-dependent manner. On apoptotic cells, CD47 was altered and/or lost and no longer activated SIRPalpha. These changes on the apoptotic cell create an environment where "don't eat me" signals are rendered inactive and "eat me" signals, including calreticulin and phosphatidylserine, congregate together and signal for removal.
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              Insertion-and-deletion-derived tumour-specific neoantigens and the immunogenic phenotype: a pan-cancer analysis

              The focus of tumour-specific antigen analyses has been on single nucleotide variants (SNVs), with the contribution of small insertions and deletions (indels) less well characterised. We investigated whether the frameshift nature of indel mutations, which create novel open reading frames and a large quantity of mutagenic peptides highly distinct from self, might contribute to the immunogenic phenotype.
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                Author and article information

                Journal
                Oncoimmunology
                Oncoimmunology
                KONI
                koni20
                Oncoimmunology
                Taylor & Francis
                2162-4011
                2162-402X
                2020
                9 January 2020
                9 January 2020
                : 9
                : 1
                : 1703449
                Affiliations
                [a ]Cell Death Research & Therapy (CDRT) unit, Department of Cellular & Molecular Medicine, KU Leuven , Leuven, Belgium
                [b ]Maastricht University Medical Center, Department of Radiation Oncology (MAASTRO Clinic), GROW-School for Oncology and Developmental Biology , Maastricht, Netherlands
                [c ]Department of Oncology, KU Leuven , Leuven, Belgium
                [d ]UZ Leuven , Leuven, Belgium
                [e ]Department of Haematology, UZ Leuven, and Department of Human Genetics, KU Leuven , Leuven, Belgium
                [f ]Sotio , Prague, Czech Republic
                [g ]Department of Immunology, 2nd Faculty of Medicine and University Hospital Motol, Charles University , Prague, Czech Republic
                [h ]Gustave Roussy Comprehensive Cancer Institute , Villejuif, France
                [i ]INSERM, U1015 , Villejuif, France
                [j ]Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 1428 , Villejuif, France
                [k ]Université Paris Sud/Paris XI , Le Kremlin-Bicêtre, France
                [l ]Equipe labellisée par la Ligue contre le cancer, Centre de Recherche des Cordeliers, Université de Paris, Sorbonne Université, INSERM U1138 , Paris, France
                [m ]Metabolomics and Cell Biology Platforms, Gustave Roussy Comprehensive Cancer Institute , Villejuif, France
                [n ]Pôle de Biologie, Hôpital Européen Georges Pompidou, AP-HP , Paris, France
                [o ]Suzhou Institute for Systems Medicine, Chinese Academy of Medical Sciences , Suzhou, China
                [p ]Department of Women’s and Children’s Health, Karolinska University Hospital , Stockholm, Sweden
                [q ]Department of Radiation Oncology, Weill Cornell Medical College , New York, NY, USA
                [r ]Sandra and Edward Meyer Cancer Center , New York, NY, USA
                [s ]Caryl and Israel Englander Institute for Precision Medicine , New York, NY, USA
                [t ]Department of Dermatology, Yale School of Medicine , New Haven, CT, USA
                [u ]Université de Paris , Paris, France
                Author notes
                CONTACT Abhishek D. Garg abhishek.garg@ 123456med.kuleuven.be Cell Death Research & Therapy (CDRT) unit, Department of Cellular & Molecular Medicine, KU Leuven , Campus Gasthuisberg, O&N1, Herestraat 49, Leuven 3000, Belgium
                Lorenzo Galluzzi deadoc80@ 123456gmail.com Weill Cornell Medical College, Stich Radiation Oncology , 525 East 68th Street, New York, NY 10065, USA
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                Author information
                http://orcid.org/0000-0003-1596-0998
                http://orcid.org/0000-0002-9334-4405
                http://orcid.org/0000-0003-2257-8500
                http://orcid.org/0000-0002-9976-9922
                Article
                1703449
                10.1080/2162402X.2019.1703449
                6959434
                32002302
                8e98e751-5de6-415e-9981-ed2f90787bc8
                © 2020 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 License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 October 2019
                : 1 November 2019
                Page count
                Figures: 1, Tables: 2, References: 394, Pages: 24
                Categories
                Review

                Immunology
                antigen-presenting cell,autophagy,cytotoxic t lymphocyte,endoplasmic reticulum stress,car t cells,cytokines,chemokines,dendritic cell,immune checkpoint blocker,type i interferon

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