@article {Hu493, author = {Wei-Shau Hu and Vinay K. Pathak}, title = {Design of Retroviral Vectors and Helper Cells for Gene Therapy}, volume = {52}, number = {4}, pages = {493--512}, year = {2000}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {During the past decade, gene therapy has been applied to the treatment of disease in hundreds of clinical trials. Various tools have been developed to deliver genes into human cells; among them, genetically engineered retroviruses are currently the most popular tool for gene delivery. Most of the systems contain vectors that are capable of accommodating genes of interest and helper cells that can provide the viral structural proteins and enzymes to allow for the generation of vector-containing infectious viral particles. Retroviridae is a family of retroviruses that differs in nucleotide and amino acid sequence, genome structure, pathogenicity, and host range. This diversity provides opportunities to use viruses with different biological characteristics to develop different therapeutic applications. Currently, a variety of retroviruses that provide distinct advantages for gene delivery has been modified and used in clinical trials. In this review, the genome structures of oncoviruses, lentiviruses, and spumaviruses are reviewed and examples of vectors derived from these viruses are described. As with any delivery tool, the efficiency, the ability to target certain tissue or cell type, the expression of the gene of interest, and the safety of retroviral-based systems are important for successful application of gene therapy. Significant efforts have been dedicated to these areas of research in recent years. Various modifications have been made to retroviral-based vectors and helper cells to alter gene expression, target delivery, improve viral titers, and increase safety. The principles and design of these modifications are discussed in this review.}, issn = {0031-6997}, URL = {https://pharmrev.aspetjournals.org/content/52/4/493}, eprint = {https://pharmrev.aspetjournals.org/content/52/4/493.full.pdf}, journal = {Pharmacological Reviews} }