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      Trial watch: TLR3 agonists in cancer therapy

      review-article
      , , , ,
      Oncoimmunology
      Taylor & Francis
      Dendritic cells, immune checkpoint blockers, polyA:U, polyI:C, Riboxxol

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          ABSTRACT

          Toll-like receptor 3 (TLR3) is a pattern recognition receptor that senses exogenous (viral) as well as endogenous (mammalian) double-stranded RNA in endosomes. On activation, TLR3 initiates a signal transduction pathway that culminates with the secretion of pro-inflammatory cytokines including type I interferon (IFN). The latter is essential not only for innate immune responses to infection but also for the initiation of antigen-specific immunity against viruses and malignant cells. These aspects of TLR3 biology have supported the development of various agonists for use as stand-alone agents or combined with other therapeutic modalities in cancer patients. Here, we review recent preclinical and clinical advances in the development of TLR3 agonists for oncological disorders.

          Abbreviations

          cDC, conventional dendritic cell; CMT, cytokine modulating treatment; CRC, colorectal carcinoma; CTL, cytotoxic T lymphocyte; DC, dendritic cell; dsRNA, double-stranded RNA; FLT3LG, fms-related receptor tyrosine kinase 3 ligand; HNSCC, head and neck squamous cell carcinoma; IFN, interferon; IL, interleukin; ISV, in situ vaccine; MUC1, mucin 1, cell surface associated; PD-1, programmed cell death 1; PD-L1, programmed death-ligand 1; polyA:U, polyadenylic:polyuridylic acid; polyI:C, polyriboinosinic:polyribocytidylic acid; TLR, Toll-like receptor

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          Most cited references173

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          The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak

          Coronavirus disease (COVID-19) is caused by SARS-COV2 and represents the causative agent of a potentially fatal disease that is of great global public health concern. Based on the large number of infected people that were exposed to the wet animal market in Wuhan City, China, it is suggested that this is likely the zoonotic origin of COVID-19. Person-to-person transmission of COVID-19 infection led to the isolation of patients that were subsequently administered a variety of treatments. Extensive measures to reduce person-to-person transmission of COVID-19 have been implemented to control the current outbreak. Special attention and efforts to protect or reduce transmission should be applied in susceptible populations including children, health care providers, and elderly people. In this review, we highlights the symptoms, epidemiology, transmission, pathogenesis, phylogenetic analysis and future directions to control the spread of this fatal disease.
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            The diverse functions of the PD1 inhibitory pathway

            T cell activation is a highly regulated process involving peptide-MHC engagement of the T cell receptor and positive costimulatory signals. Upon activation, coinhibitory 'checkpoints', including programmed cell death protein 1 (PD1), become induced to regulate T cells. PD1 has an essential role in balancing protective immunity and immunopathology, homeostasis and tolerance. However, during responses to chronic pathogens and tumours, PD1 expression can limit protective immunity. Recently developed PD1 pathway inhibitors have revolutionized cancer treatment for some patients, but the majority of patients do not show complete responses, and adverse events have been noted. This Review discusses the diverse roles of the PD1 pathway in regulating immune responses and how this knowledge can improve cancer immunotherapy as well as restore and/or maintain tolerance during autoimmunity and transplantation.
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              Neoantigen vaccine generates intratumoral T cell responses in phase Ib glioblastoma trial

              Neoantigens, which are derived from tumour-specific protein-coding mutations, are exempt from central tolerance, can generate robust immune responses1,2 and can function as bona fide antigens that facilitate tumour rejection3. Here we demonstrate that a strategy that uses multi-epitope, personalized neoantigen vaccination, which has previously been tested in patients with high-risk melanoma4-6, is feasible for tumours such as glioblastoma, which typically have a relatively low mutation load1,7 and an immunologically 'cold' tumour microenvironment8. We used personalized neoantigen-targeting vaccines to immunize patients newly diagnosed with glioblastoma following surgical resection and conventional radiotherapy in a phase I/Ib study. Patients who did not receive dexamethasone-a highly potent corticosteroid that is frequently prescribed to treat cerebral oedema in patients with glioblastoma-generated circulating polyfunctional neoantigen-specific CD4+ and CD8+ T cell responses that were enriched in a memory phenotype and showed an increase in the number of tumour-infiltrating T cells. Using single-cell T cell receptor analysis, we provide evidence that neoantigen-specific T cells from the peripheral blood can migrate into an intracranial glioblastoma tumour. Neoantigen-targeting vaccines thus have the potential to favourably alter the immune milieu of glioblastoma.
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                Author and article information

                Journal
                Oncoimmunology
                Oncoimmunology
                Oncoimmunology
                Taylor & Francis
                2162-4011
                2162-402X
                2 June 2020
                2020
                2 June 2020
                : 9
                : 1
                : 1771143
                Affiliations
                [a ]Equipe Labellisée Par La Ligue Contre Le Cancer, Université De Paris, Sorbonne Université, INSERM U1138, Centre De Recherche Des Cordeliers; , Paris, France
                [b ]Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus; , Villejuif, France
                [c ]Gustave Roussy Cancer Campus; , Villejuif, France
                [d ]Faculty of Medicine Kremlin Bicêtre, Université Paris Sud, Paris Saclay; , Kremlin Bicêtre, France
                [e ]Department of Radiation Oncology, Weill Cornell Medical College; , New York, NY, USA
                [f ]Sandra and Edward Meyer Cancer Center; , New York, NY, USA
                [g ]Caryl and Israel Englander Institute for Precision Medicine; , New York, NY, USA
                [h ]Department of Dermatology, Yale School of Medicine; , New Haven, CT, USA
                [i ]Université De Paris; , Paris, France
                [j ]Equipe Labellisée Ligue Contre Le Cancer, INSERM; , Villejuif, France
                [k ]Center of Clinical Investigations in Biotherapies of Cancer (CICBT) 1428; , Villejuif, France
                [l ]AP-HP, Hôpital Européen Georges Pompidou; , Paris, France
                [m ]Suzhou Institute for Systems Medicine, Chinese Academy of Medical Sciences; , Suzhou, China
                [n ]Karolinska Institute, Department of Women’s and Children’s Health, Karolinska University Hospital; , Stockholm, Sweden
                Author notes
                CONTACT Guido Kroemer kroemer@ 123456orange.fr Equipe Labellisée Par La Ligue Contre Le Cancer, Université De Paris, Sorbonne Université, INSERM U1138, Centre De Recherche Des Cordeliers, Paris, France
                [*]

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                Author information
                https://orcid.org/0000-0003-2257-8500
                https://orcid.org/0000-0003-1596-0998
                https://orcid.org/0000-0002-9334-4405
                Article
                1771143
                10.1080/2162402X.2020.1771143
                7466857
                32934877
                5610aa32-c732-4c2b-a133-77f6cee0e2bd
                © 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.

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                Figures: 0, Tables: 1, References: 242, Pages: 1
                Categories
                Review
                Review

                Immunology
                dendritic cells,immune checkpoint blockers,polya:u,polyi:c,riboxxol
                Immunology
                dendritic cells, immune checkpoint blockers, polya:u, polyi:c, riboxxol

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