Titlebook: Inflammation and Immunity in Cancer; Tsukasa Seya,Misako Matsumoto,Noriyuki Sato Book 2015 Springer Japan 2015 Immunotherapy.adjuvant.anti

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Host Factors Involved in the Propagation and Pathogenesis of Hepatitis C Virus,apies. Furthermore, it remains unclear whether elimination of HCV by DAAs can protect against HCV-induced liver diseases. In this review, we summarize our current data regarding molecular mechanisms of HCV-induced liver diseases.

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Development of Immunotherapy for Hepatocellular Carcinoma, HCC patients with peptide vaccine. In this chapter, we summarize the results of previous studies using DC and peptide vaccine, including our own data, and describe the prospects of immunotherapy for HCC.

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,Enhancement of Efficacy of Wilms’ Tumor Gene , Product-derived Peptide Cancer Vaccine by Co-adminisall skeleton (BCG-CWS), which is well-known to activate dendritic cells (DCs), i.e., activate innate immunity, could induce and/or activate WT1-specific CTLs in combination with WT1 peptide vaccination. Interferon (IFN)-β is a type I IFN, and is known for its various anticancer properties. Co-admini

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Regulation of Antigen Presentation by Dendritic Cells and Its Application to Cancer Immunotherapy,-receptor (TLR) ligands, type 1 cytokines, and CD40/40L interaction. On the other hand, IL-6 produced in tumor microenvironments caused dysfunction of DCs through reduction of MHC class II expression and IL-12 production. It has recently been reported that zinc transporter-mediated intracellular zin

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Progress in Clinical Use of CC Chemokine Receptor 4 Antibody for Regulatory T Cell Suppression,n immune regulation, just as the regulatory molecules in the immune checkpoint become targets for the development of novel tumor immunotherapy, they may also become a target for development. Several reports have suggested that Tregs that infiltrate tumor sites as well as regulatory signals for immun

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theory and its application to the modeling of the constitutive and the evolution equations of damaged materials are descried as a systematic basis for the subsequent development throughout the book.  . .Part I978-94-007-9960-8978-94-007-2666-6Series ISSN 0925-0042 Series E-ISSN 2214-7764