Why are Viruses Used in Gene Therapy

Gene therapy is the introduction of foreign genetic material into body cells to compensate for abnormal genes or to synthesize beneficial proteins. The efficient transfer of genetic material into the target cell is essential to achieve the desired therapeutic effect. In order to facilitate gene transfer, either viral-based or non-viral based vectors can be used as the delivery system. Viruses are a type of widely-used vectors to transfer foreign DNA into a cell. The most common types of viral vectors used in gene transfer are retrovirus, adenovirus, and adeno-associated virus. The ability of viruses to infect cells is the key feature that allows viruses to be used as vectors in gene therapy.

Key Areas Covered

1. What is Gene Therapy
     – Definition, Methods, Vectors
2. Why are Viruses Used in Gene Therapy
     – Viral Vectors for Gene Therapy

Key Terms: Alteration of Gene Expression, Functional Genes, Homologous Recombination, Infectious Life Cycle, Gene Therapy, Viruses, Vectors

What is Gene Therapy

Gene therapy is the insertion of normal DNA directly into a cell in order to correct genetic defects. The two main approaches to gene therapy are either introducing a gene that encodes for a functional protein or transferring of an entity that alters the expression of a gene in the genome.

Efficient delivery methods such as vectors facilitate gene transfer into the cells during gene therapy. Two types of vectors are used in gene therapy: viral vectors and non-viral vectors. The nonviral-based delivery systems can be plasmids or chemically-synthesized oligonucleotides. Optimal vector selection is based on several parameters:

Why are Viruses Used in Gene Therapy

Due to the infectious lifecycle, viruses are widely-used in gene transfer during gene therapy. Generally, viruses infect host cells and replicate inside the host cell by integrating viral DNA into the genome of the host. Hence, the interested DNA fragments can be introduced into the cell by packing it inside the viral particles. The three main types of viral vectors used in gene therapy are retroviruses, adenoviruses, and adeno-associated viruses (AAV). In addition, herpes simplex virus-1 (HSV-1), baculovirus, vaccine virus are also used as vectors. The use of adenoviruses in gene therapy is shown in figure 1.

Figure 1: Adenovirus in Gene Therapy

In order to use a virus as a vector during gene therapy, its virulent genes are replaced with the gene of interest. The rest of the viral genome remains the same. The infected viral elements govern the homologous recombination of the modified viral genome to the host genome. The location for homologous recombination can be determined by the sequence of the recombining elements. Once integrated into the genome, the introduced DNA is stably expressed and replicates along with the host’s genome.

Conclusion

Gene therapy is a technology to treat defective genes in the genome by introducing new DNA. Both viral and nonviral DNA delivery systems facilitate the transfer of new DNA into cells. Viral delivery systems introduce new DNA into the host cells during infection. New DNA stably integrates into the host’s genome by homologous recombination, expressing and replicating along with the genome.

Reference:

1. PONDER, KATHERINE PARKER. “Vectors of Gene Therapy.” An Introduction to Molecular Medicine and Gene Therapy., Wiley-Liss, Inc., 2001, pp. 77–112. Available here.

Image Courtesy:

1. “Gene therapy” (Public Domain) via Commons Wikimedia

ncG1vNJzZmiolZm2oq2NnKamZ6edxm6t0Z5kr6GiqsCmv4yuqp6cXZ67brPEp5xmrJiav6K82Gg%3D