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|a Translational immunotherapy of brain tumors /
|c edited by John H. Sampson.
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|a London, United Kingdom :
|b Academic Press, an imprint of Elsevier,
|c 2017.
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|a 1 online resource
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|a Front Cover; TRANSLATIONALIMMUNOTHERAPY OFBRAIN TUMORS; TRANSLATIONALIMMUNOTHERAPYOF BRAINTUMORS; Copyright; Contents; List of Contributors; Introduction to Translational Immunotherapy for Brain Tumors; TRANSLATIONAL IMMUNOTHERAPY FOR BRAIN TUMORS SUMMARY; PRIMER ON MALIGNANT GLIOMAS; THE POTENTIAL OF CANCER IMMUNOTHERAPY; CHALLENGES OF BRAIN TUMOR IMMUNOTHERAPY; CHAPTER OVERVIEW; References; I -- IIMMUNOLOGICALFEATURES OF BRAINTUMORS; 1 -- An Introduction to Immunotherapy in the Treatment of Brain Tumors; INTRODUCTION; THE IMMUNE RESPONSE; IMMUNE TOLERANCE
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|a UNIQUE ASPECTS OF THE CENTRAL NERVOUS SYSTEM IMMUNE RESPONSEThe Blood-Brain Barrier; The CNS Lymphatic System; Antigen Presentation in the CNS; CANCER IMMUNOTHERAPIES; References; 2 -- Immune Constitution of Patients With Brain Tumors; BACKGROUND AND DISCOVERY; CURRENT UNDERSTANDING: ANALYZING SYSTEMIC IMMUNE DYSFUNCTION; Lymphopenia; Lymphocyte Dysfunction; Regulatory T Cells; CURRENT UNDERSTANDING: ANALYZING THE TUMOR; Cytokine Dysregulation; Signal Transducer and Activator of Transcription-3; Indoleamine 2,3 Dioxygenase; CLINICAL OPPORTUNITIES
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|a Countering T Cell Dysfunction: Immune Checkpoint BlockadeCountering Regulatory T Cells and Lymphopenia; Countering Cytokine Dysregulation; Countering Tumor STAT3 and IDO Expression; CONCLUSION; References; 3 -- The Role of Regulatory T Cells and Indoleamine-2,3-dioxygenase in Brain Tumor Immunosuppression; BACKGROUND AND DISCOVERY; ORIGIN OF TREGS; FUNCTION OF TREGS; TREGS IN THE CANCER IMMUNITY CYCLE; TREGS AND GLIOMA; TRYPTOPHAN CATABOLISM IN IMMUNITY AND IN CANCER; IDO1, IDO2, AND TDO; THE AHR; MECHANISMS OF IMMUNE REGULATION BY THE IDO PATHWAY; THE IDO PATHWAY IN CANCER AND IN GLIOMA
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|a TARGETING TREGS IN PRECLINICAL MODELTARGETING IDO IN PRECLINICAL MODELS; CLINICAL TRIAL DATA; CONCLUSION; References; 4 -- The Role of Myeloid-Derived Suppressor Cells in Immunosuppression in Brain Tumors; BACKGROUND AND DISCOVERY OF THE MYELOID CELL; MDSCs in Mice; MDSCs in Humans; MDSC Activation, Proliferation, Migration, and Expansion; Suppressive Mechanisms Mediated by MDSCs; Suppression via Arg1 and iNOS; Suppression via Reactive Oxygen Species; Suppression via Peroxynitrite; Other Immunosuppressive Mechanisms; MDSCs in Glioma Development; PRECLINICAL DATA: TARGETING THE MDSC POPULATION
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|a Includes index.
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|a Online resource; title from PDF title page (ScienceDirect, viewed February 17, 2017).
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|a Includes bibliographical references and index.
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650 |
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|a Brain
|x Tumors
|x Immunotherapy.
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1 |
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|a Brain Neoplasms
|x therapy
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|a Electronic books.
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|a Internet Resources.
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|a Sampson, John H.,
|e editor.
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|i Print version:
|t Translational immunotherapy of brain tumors.
|d London, United Kingdom : Academic Press, an imprint of Elsevier, 2017
|z 0128024208
|z 9780128024201
|w (OCoLC)959874904
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|a Chemokine and Cytokine ApproachesDifferentiation; IL-4Rα Targeting; Arginase 1; Fibrinogen-Like Protein 2 Targeting; M1 Polarization or M2 Blockade; CLINICAL APPROACHES TO TARGETING MDSCS; References; 5 -- Tumor-Specific Mutations in Gliomas and Their Implications for Immunotherapy; INTRODUCTION; MUTATIONS AS IMMUNOTHERAPEUTIC TARGETS; ISOCITRATE DEHYDROGENASE 1 MUTATIONS IN GLIOMAS; IDH1 MUTATIONS AS AN IMMUNOTHERAPEUTIC TARGET; PRECLINICAL INVESTIGATIONS: IDH1-R132H PEPTIDE VACCINES; CLINICAL INVESTIGATIONS: IDH1-R132H PEPTIDE VACCINES
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