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      Bispecific Immunomodulatory Antibodies for Cancer Immunotherapy

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          Abstract

          The recent advances in the field of immuno-oncology have dramatically changed the therapeutic strategy against advanced malignancies. Bispecific antibody-based immunotherapies have gained momentum in preclinical and clinical investigations following the regulatory approval of the T cell–redirecting antibody blinatumomab. In this review, we focus on emerging and novel mechanisms of action of bispecific antibodies interacting with immune cells with at least one of their arms to regulate the activity of the immune system by redirecting and/or reactivating effector cells toward tumor cells. These molecules, here referred to as bispecific immunomodulatory antibodies, have the potential to improve clinical efficacy and safety profile and are envisioned as a second wave of cancer immunotherapies. Currently, there are more than 50 bispecific antibodies under clinical development for a range of indications, with promising signs of therapeutic activity. We also discuss two approaches for in vivo secretion, direct gene delivery, and infusion of ex vivo gene-modified cells, which may become instrumental for the clinical application of next-generation bispecific immunomodulatory antibodies.

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          Molecular and cellular insights into T cell exhaustion.

          In chronic infections and cancer, T cells are exposed to persistent antigen and/or inflammatory signals. This scenario is often associated with the deterioration of T cell function: a state called 'exhaustion'. Exhausted T cells lose robust effector functions, express multiple inhibitory receptors and are defined by an altered transcriptional programme. T cell exhaustion is often associated with inefficient control of persisting infections and tumours, but revitalization of exhausted T cells can reinvigorate immunity. Here, we review recent advances that provide a clearer molecular understanding of T cell exhaustion and reveal new therapeutic targets for persisting infections and cancer.
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            Fundamental Mechanisms of Immune Checkpoint Blockade Therapy

            Immune checkpoint blockade is able to induce durable responses across multiple types of cancer, which has enabled the oncology community to begin to envision potentially curative therapeutic approaches. However, the remarkable responses to immunotherapies are currently limited to a minority of patients and indications, highlighting the need for more effective and novel approaches. Indeed, an extraordinary amount of preclinical and clinical investigation is exploring the therapeutic potential of negative and positive costimulatory molecules. Insights into the underlying biological mechanisms and functions of these molecules have, however, lagged significantly behind. Such understanding will be essential for the rational design of next-generation immunotherapies. Here, we review the current state of our understanding of T-cell costimulatory mechanisms and checkpoint blockade, primarily of CTLA4 and PD-1, and highlight conceptual gaps in knowledge.Significance: This review provides an overview of immune checkpoint blockade therapy from a basic biology and immunologic perspective for the cancer research community. Cancer Discov; 8(9); 1069-86. ©2018 AACR.
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              Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma

              Nivolumab combined with ipilimumab resulted in longer progression-free survival and a higher objective response rate than ipilimumab alone in a phase 3 trial involving patients with advanced melanoma. We now report 3-year overall survival outcomes in this trial.
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                Author and article information

                Journal
                Clin Cancer Res
                Clin Cancer Res
                Clinical Cancer Research
                American Association for Cancer Research
                1078-0432
                1557-3265
                15 October 2021
                09 June 2021
                : 27
                : 20
                : 5457-5464
                Affiliations
                [1 ]Cancer Immunotherapy Unit (UNICA), Department of Immunology, Hospital Universitario 12 de Octubre, Madrid, Spain.
                [2 ]Immuno-Oncology and Immunotherapy Group, Instituto de Investigación Sanitaria 12 de Octubre (imas12), Madrid, Spain.
                Author notes
                [* ] Corresponding Author: Luis Alvarez-Vallina, Cancer Immunotherapy Unit, Hospital Universitario 12 de Octubre, Madrid, 28041, Spain. E-mail: lav.imas12@ 123456h12o.es

                Clin Cancer Res 2021;27:5457–64

                Author information
                https://orcid.org/0000-0001-5085-7756
                https://orcid.org/0000-0002-0446-9629
                https://orcid.org/0000-0003-3053-6757
                Article
                CCR-20-3770
                10.1158/1078-0432.CCR-20-3770
                9306338
                34108185
                18cae167-1b48-4cd0-9052-27700a6a2170
                ©2021 The Authors; Published by the American Association for Cancer Research

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs International 4.0 License.

                History
                : 01 March 2021
                : 25 April 2021
                : 21 May 2021
                Page count
                Pages: 8
                Funding
                Funded by: Carlos III Health Institute;
                Award ID: PI20/01030
                Funded by: Spanish Ministry of Science and Innovation;
                Award ID: SAF2017–89437-P
                Award ID: RTC-2017–5944–1
                Funded by: CRIS Cancer Foundation;
                Award ID: FCRIS-IFI-2018
                Funded by: Spanish Association Against Cancer;
                Award ID: 19084
                Funded by: Spanish Ministry of Science and Innovation;
                Award ID: PRE2018–083445
                Categories
                Review
                Biological Agents & Therapies
                Immunology
                Antibodies/Immunoconjugates
                Immunomodulation
                Immunotherapy
                Antibody Immunotherapy
                Protein Technologies

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