Vector Targeting for Therapeutic Gene Delivery

Vector Targeting for Therapeutic Gene Delivery

Curiel, David T.; Douglas, Joanne T.

John Wiley and Sons Ltd

08/2002

710

Dura

Inglês

9780471434795

0471434795

15 a 20 dias

1133

This book presents the most recent advances in target definition technology and provides a detailed overview on the rational design of targeted vectors for gene therapy. This unique reference integrates all of the allied sciences relevant to vector targeting by providing a theoretical framework for advanced vector design.
Preface. Contributors. PART I: TRANSDUCTIONALLY TARGETED VECTORS--NONVIRAL. Alternative Strategies for Targeted Delivery of Nucleic Acid-Liposome Complexes (N. Templeton). Targeted Gene Delivery via Lipidic Vectors (S. Li, et al.). Immunoliposomes: A Targeted Delivery Tool for Cancer Treatment (K. Pirollo, et al.). Receptor-Directed Gene Delivery Using Molecular Conjugates (A. Ziady & P. Davis). PART II: TRANSDUCTIONALLY TARGETED VECTORS--VIRAL. Pseudotyping of Adenoviral Vectors (M. Havenga, et al.). Targeting of Adenoviral Gene Therapy Vectors: The Flexibility of Chemical and Molecular Conjugation (H. Haisma & M. Rots). Genetic Targeting of Adenoviral Vectors (T. Wickham). Strategies to Alter the Tropism of Adenoviral Vectors via Genetic Capsid Modification (D. Curiel). Conjugate-Based Targeting of Adeno-Associated Virus Vectors (S. Ponnazhagan, et al.). Receptor Targeting of Adeno-Associated Virus Vectors (H. Buning, et al.). Mechanisms of Retroviral Particle Maturation and Attachment (A. Miyanohara & T. Friedmann). Targeting Retroviral Vectors Using Molecular Bridges (J. Young). Genetic Targeting of Retroviral Vectors (D. Dingli & S. Russell). Genetic Engineering of Targeted Retroviral Vectors (E. Gordon, et al.). Targeting Measles Virus Entry (A. Hammond, et al.). Targeting of Poliovirus Replicons to Neurons in the Central Nervous System (C. Morrow, et al.). Generation of Safe, Targetable Sindbis Vectors that Have the Potential for Direct In Vivo Gene Therapy (D. Meruelo, et al.). Redirecting the Tropism of HSV-1 for Gene Therapy Applications (Q. Bai, et al.). Engineering Targeted Bacteriophage as Evolvable Vectors for Therapeutic Gene Delivery (D. Larocca & A. Baird). Targeting Bacteriophage Vectors (I. Saggio). PART III: TRANSCRIPTIONAL TARGETING. Tumor/Tissue Selective Promoters (M. Fernandez & N. Lemoine). Promoter Optimization and Artificial Promoters for Transcriptional Targeting in Gene Therapy (D. Nettelbeck, et al.). Physiological Targeting (K. Binley). Clostridium-Mediated Transfer of Therapeutic Proteins to Solid Tumors (P. Lambin, et al.). PART IV: TARGET DEFINITION. Selection of Peptides on Phage (M. Barry, et al.). Antibody Phage Display Libraries for Use in Therapeutic Gene Targeting (P. Rohrbach & S. Dubel). Single-Chain Fv Fragments from Phage Display Libraries (R. Kontermann). Retroviral Particle Display for Complex Glycosylated and Disulfide-Bonded Protein Domains (S. Kayman). Cell Surface Display and Cytometric Screening for Protein Ligand Isolation and Engineering (P. Daugherty). PART V: MONITORING OF TARGETING. Monitoring Gene Therapy By Positron Emission Tomography (H. Herschman, et al.). Index.
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