Isbn: 9781493924318 - gene therapy for hiv and chronic infections (advances in experimental medicine and biology, 848, band 848) (3 Ergebnisse)

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  • Sprache: Englisch

    Verlag: Springer, 2015

    1493924311 / 9781493924318

    Serie: Buch 65 von 490 - Advances in Experimental Medicine and Biology

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    Zustand: New. In English.

  • Sprache: Englisch

    Verlag: Springer, 2015

    1493924311 / 9781493924318

    Serie: Buch 65 von 490 - Advances in Experimental Medicine and Biology

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    Hardcover. Zustand: Brand New. 1st edition. 236 pages. 9.50x6.00x0.75 inches. In Stock.

  • Sprache: Englisch

    Verlag: Springer New York, 2015

    1493924311 / 9781493924318

    Serie: Buch 65 von 490 - Advances in Experimental Medicine and Biology

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    Zustand: Sehr gut. Zustand: Sehr gut | Sprache: Englisch | Produktart: Bücher | This book centers  on gene therapy and gene transfer approaches to prevent or treat chronic virus infections. The main focus is on the Big Three: human immunodeficiency virus (HIV-1), hepatitis B virus (HBV) and hepatitis C virus (HCV). Ample anti-HIV drugs are currently available in the clinic and the development of an effective combination therapy has dramatically improved the lifespan and quality of life of infected individuals. A similar trend can already be recognized for HBV and HCV: the development of multiple (directly acting) antiviral drugs and plans to control or even cure the infection. However, approaches that help prevent infection, or which provide long-lasting treatment (such as a cure) remain important goals.   Immunization through gene transfer vehicles encoding immunogenic viral proteins shows promise in preventing infections with complex, highly variable, viruses such as HIV-1 or HCV. Gene therapy applications for virus infections have been discussed since the early 1990¿s. Whereas a true cure seems difficult to achieve for HIV-1 due to its intrinsic property to deposit its genome into that of the host, such attempts may be within reach for HCV where spontaneous viral clearance occurs in a small percentage of the infected individuals. The prospect of original gene therapy approaches may provide alternative ways to reach the same endpoint by, for example, silencing of CCR5 expression post-transcriptionally. Many alternative antiviral strategies have been developed based on a variety of novel molecular methods: e.g. ribozymes. Some studies have progressed towards pre-clinical animal models and a few antiviral gene therapies have progressed towards clinical trials. This book provides an overview of this rapidly progressing field, while focusing on the interface of gene therapy and immunology/vaccinology.…