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Adeno-Associated Virus [electronic resource] : Methods and Protocols / edited by Richard O. Snyder, Philippe Moullier.

Contributor(s): Series: Methods in Molecular Biology, Methods and Protocols ; 807Publisher: Totowa, NJ : Humana Press, 2011Description: XIII, 462 p. 43 illus., 20 illus. in color. online resourceContent type:
  • text
Media type:
  • computer
Carrier type:
  • online resource
ISBN:
  • 9781617793707
Subject(s): Genre/Form: Additional physical formats: Printed edition:: No titleDDC classification:
  • 591.35 23
LOC classification:
  • QH432
Online resources:
Contents:
Adeno-Associated Virus Biology -- Design and Construction of Functional AAV Vectors -- AAV Capsid Structure and Cell Interactions -- Exploiting Natural Diversity of AAV for the Design of Vectors With Novel Properties -- Gene Therapy in Skeletal Muscle Mediated by Adeno-Associated Virus (AAV) Vectors -- AAV-Mediated Liver-Directed Gene Therapy -- Recombinant AAV Delivery to the Central Nervous System -- AAV Mediated Gene Therapy for Retinal Degenerative Diseases -- Adeno-Associated Virus Vector Delivery to the Heart -- Evaluation of the Fate of rAAV Genomes Following in vivo Administration -- Measuring Immune Responses to Recombinant AAV Gene Transfer -- Modification and Labeling of AAV Vector Particles -- AAV-mediated Gene Targeting -- Preclinical Study Design for rAAV -- Biodistribution and Shedding of AAV Vectors -- Production and Purification of Recombinant Adeno-Associated Vectors -- rAAV Vector Product Characterization and Stability Studies -- rAAV Human Trial Experience.
In: Springer eBooksSummary: Today, progress in rAAV-mediated gene transfer is so robust that long-term, efficient, and regulatable transgene expression is reproducibly achieved in large animal models. The complexity of  gene transfer agents in the context of their clinical use requires investigators from a wide variety of backgrounds to have an understanding — or at least an appreciation of — the regulatory environment and constraints that affect vector design, manufacturing, pre-clinical testing, and clinical use, with an emphasis on patient protection. In Adeno-Associated Virus: Methods and Protocols, experts from the United States and Europe have contributed current knowledge of this multi-dimensional field relating to the biology of AAV, rAAV vector design, vector manufacturing and product testing, performance of rAAV vectors in major organs, rAAV-related immunological issues, design of animal and clinical studies, and clinical experience. Written in the successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.   Authoritative and accessible, Adeno-Associated Virus: Methods and Protocols provides a complete and comprehensive understanding of this multi-disciplinary and rapidly progressing field.
Item type: eBooks
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Adeno-Associated Virus Biology -- Design and Construction of Functional AAV Vectors -- AAV Capsid Structure and Cell Interactions -- Exploiting Natural Diversity of AAV for the Design of Vectors With Novel Properties -- Gene Therapy in Skeletal Muscle Mediated by Adeno-Associated Virus (AAV) Vectors -- AAV-Mediated Liver-Directed Gene Therapy -- Recombinant AAV Delivery to the Central Nervous System -- AAV Mediated Gene Therapy for Retinal Degenerative Diseases -- Adeno-Associated Virus Vector Delivery to the Heart -- Evaluation of the Fate of rAAV Genomes Following in vivo Administration -- Measuring Immune Responses to Recombinant AAV Gene Transfer -- Modification and Labeling of AAV Vector Particles -- AAV-mediated Gene Targeting -- Preclinical Study Design for rAAV -- Biodistribution and Shedding of AAV Vectors -- Production and Purification of Recombinant Adeno-Associated Vectors -- rAAV Vector Product Characterization and Stability Studies -- rAAV Human Trial Experience.

Today, progress in rAAV-mediated gene transfer is so robust that long-term, efficient, and regulatable transgene expression is reproducibly achieved in large animal models. The complexity of  gene transfer agents in the context of their clinical use requires investigators from a wide variety of backgrounds to have an understanding — or at least an appreciation of — the regulatory environment and constraints that affect vector design, manufacturing, pre-clinical testing, and clinical use, with an emphasis on patient protection. In Adeno-Associated Virus: Methods and Protocols, experts from the United States and Europe have contributed current knowledge of this multi-dimensional field relating to the biology of AAV, rAAV vector design, vector manufacturing and product testing, performance of rAAV vectors in major organs, rAAV-related immunological issues, design of animal and clinical studies, and clinical experience. Written in the successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.   Authoritative and accessible, Adeno-Associated Virus: Methods and Protocols provides a complete and comprehensive understanding of this multi-disciplinary and rapidly progressing field.

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