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  • 1
    Online-Ressource
    Online-Ressource
    New York, NY : Springer-Verlag New York
    UID:
    gbv_613898753
    Umfang: Online-Ressource , v.: digital
    Ausgabe: Online-Ausg. Springer eBook Collection. Biomedical and Life Sciences Electronic reproduction; Available via World Wide Web
    ISBN: 9781441901699
    Inhalt: "The principle of cancer immune therapy remains the stimulation of the immune system to control and destroy tumors, but the scope is expanded in steady and fast pace, the approach is modernized every few years, new molecules are revealed annually, and the understanding of the mechanisms is getting deeper and deeper. Targeted Cancer Immune Therapy covers cytokine immune therapy, cell-based immune therapy, and targeted immune therapy. In each of these three sections, only the novel aspects of immune therapy were selectively described instead of attempting to cover any historical achievement. In the first section, Cytokine Immune Therapy, the IL12 family, IL18, IL21, IL24, IL28, and IL29 were heavily discussed in regard to the anti-tumor function and application in treating tumors. In the second section, Cell-based Immune Therapy, the focus was given to engineering potent immune regulatory or effector cells such as dendritic cells, T cells, and stem cells. The cell engineering design is primarily based on the increased understanding of the interaction of tumor antigen presenting cells, antigen specific effector cells, and the tumor microenvironment. In the third section, Targeted Immune Therapy, the focus was given on rearticulating the antibody therapy for boosting immune response, which includes immunocytokines, ""T-body"", and tumor targeted CpG ODN. Immunocytokines represent a new class of biopharmaceuticals composed of two well known immune components - antibodies and cytokines - with the unique ability to target cytokines to the tumor microenvironment and thereby activate antitumor responses. Some or all of these innovative approaches may ultimately become the future effective immune therapy for treating malignancy."
    Anmerkung: Includes bibliographical references and index , Targeted Cancer Immune Therapy; Preface; Contents; Contributors; Role of IL12 Family in Regulation of Antitumor Immune Response; IL-18 in Regulation of Antitumor Immune Response and Clinical Application; Interleukin-21 and Cancer Therapy; IL-24 in Regulation of Antitumor Immune Response and in Signaling; IL-28 and IL-29 in Regulation of Antitumor Immune Response and Induction of Tumor Regression; Passive and Active Tumor Homing Cytokine Therapy; New Strategies to Improve Tumor Cell Vaccine Therapy; Modification of Dendritic Cells to Enhance Cancer Vaccine Potency , Dendritic Cell Vaccines for Immunotherapy of Cancer: Challenges in Clinical TrialsA "Toll Bridge" for Tumor-Specific T Cells; Engineering Adult Stem Cells for Cancer Immunotherapy; Animal Models for Evaluating Immune Responses of Human Effector Cells In Vivo; CD40 Stimulation and Antitumor Effects; Immunocytokines: A Novel Approach to Cancer Immune Therapy; Immune Escape: Role of Indoleamine 2,3-Dioxygenase in Tumor Tolerance; Adoptive Transfer of T-Bodies: Toward an Effective Cancer Immunotherapy; Targeting Toll-Like Receptor for the Induction of Immune and Antitumor Responses , Manipulating TNF Receptors to Enhance Tumor Immunity for the Treatment of CancerIndex , Electronic reproduction; Available via World Wide Web
    Weitere Ausg.: ISBN 9781441901705
    Weitere Ausg.: ISBN 9781441901699
    Sprache: Englisch
    URL: Volltext  (lizenzpflichtig)
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    UID:
    almahu_9949419186302882
    Umfang: XI, 343 p. , online resource.
    Ausgabe: 1st ed. 2009.
    ISBN: 9781441901705
    Inhalt: Cancer has surpassed heart disease as the number one killer in the world, and standard cancer therapy such as radiation, chemotherapy, and surgery may have reached its plateau in further improving the outcome of treated patients. Biological therapies combined with other treatment approaches may be the next X-factor to greatly extend survival time and improve patients' quality of life. One of the most developed fields in biological therapy is immune therapy, which has stemmed into many branches due to its significance and the tremendous effort by a large population of scientists. Tumor-targeted antibody therapy has been successfully used for treating some types of tumors, and the first tumor vaccine against ovarian cancer has been developed for clinical application. Targeted Cancer Immune Therapy provides comprehensive coverage of novel immune therapeutic approaches, including cytokine therapy, engineered cell therapy, and the application of tumor-targeted antibodies for generating tumor-specific cell therapy, TLR ligand therapy, and cytokine therapy. In the section "Cytokine Immune Therapy," the authors review relatively new cytokine family members, such as the IL12 family, IL18, IL21, IL24, IL28, and IL29, in regard to the anti-tumor function and application in treating tumors. The strategy for targeting and retaining cytokines in the tumor microenvironment is also reviewed. The section "Cell-based Immune Therapy" focuses on reviewing "state of the art" approaches for engineering potent immune regulatory or effector cells, such as dendritic cells, T cells, and stem cells, for tumor targeting and initiation of tumor specific immune response. In the section "Targeted Immune Therapy," the authors rearticulate antibody therapy for boosting immune response, which includes immunocytokines, "T-body," and tumor targeted CpG ODN. Some or all of these innovative approaches may ultimately become effective future immune therapies for treating malignancy.
    Anmerkung: Cytokine Immune Therapy -- Role of IL12 Family in Regulation of Antitumor Immune Response -- IL-18 in Regulation of Antitumor Immune Response and Clinical Application -- Interleukin-21 and Cancer Therapy -- IL-24 in Regulation of Antitumor Immune Response and in Signaling -- IL-28 and IL-29 in Regulation of Antitumor Immune Response and Induction of Tumor Regression -- Passive and Active Tumor Homing Cytokine Therapy -- Cell-based Immune Therapy -- New Strategies to Improve Tumor Cell Vaccine Therapy -- Modification of Dendritic Cells to Enhance Cancer Vaccine Potency -- Dendritic Cell Vaccines for Immunotherapy of Cancer: Challenges in Clinical Trials -- A "Toll Bridge" for Tumor-Specific T Cells -- Engineering Adult Stem Cells for Cancer Immunotherapy -- Animal Models for Evaluating Immune Responses of Human Effector Cells In Vivo -- Targeted Immune Therapy -- CD40 Stimulation and Antitumor Effects -- Immunocytokines: A Novel Approach to Cancer Immune Therapy -- Immune Escape: Role of Indoleamine 2,3-Dioxygenase in Tumor Tolerance -- Adoptive Transfer of T-Bodies: Toward an Effective Cancer Immunotherapy -- Targeting Toll-Like Receptor for the Induction of Immune and Antitumor Responses -- Manipulating TNF Receptors to Enhance Tumor Immunity for the Treatment of Cancer.
    In: Springer Nature eBook
    Weitere Ausg.: Printed edition: ISBN 9781441901897
    Weitere Ausg.: Printed edition: ISBN 9781441901699
    Weitere Ausg.: Printed edition: ISBN 9781493939916
    Sprache: Englisch
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Buch
    Buch
    New York, NY [u.a.] : Springer-Verlag
    UID:
    kobvindex_ZLB15065939
    Umfang: XI, 343 Seiten , Ill., graph. Darst. , 235 mm x 155 mm
    Ausgabe: 1. ed.
    ISBN: 9781441901699
    Anmerkung: Text engl.
    Sprache: Englisch
    Schlagwort(e): Krebs 〈Medizin〉 ; Therapie
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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