Synthetic Biology Approaches for Engineering Next-Generation Adenoviral Gene Therapies
Source abstract
Abstract
Synthetic biology centers on the design and modular assembly of biological parts so as to construct artificial biological systems. Over the past decade, synthetic biology has blossomed into a highly productive field, yielding advances in diverse areas such as neuroscience, cell-based therapies, and chemical manufacturing. Similarly, the field of gene therapy has made enormous strides both in proof-of-concept studies and in the clinical setting. One viral vector of increasing interest for gene therapy is the adenovirus (Ad). A major part of the Ad's increasing momentum comes from synthetic biology approaches to Ad engineering. Convergence of gene therapy and synthetic biology has enhanced Ad vectors by mitigating Ad toxicity in vivo, providing precise Ad tropisms, and incorporating genetic circuits to make smart therapies which adapt to environmental stimuli. Synthetic biology engineering of Ad vectors may lead to superior gene delivery and editing platforms which could find applications in a wide range of therapeutic contexts.
Source: europepmc · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: CRISPR and Genetic Engineering · Virus-based gene therapy research · Viral Infectious Diseases and Gene Expression in Insects
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, Missouri 63110, United States
Department of Radiation Oncology, Washington University in St. Louis, St. Louis, Missouri 63110, United States
Funding
National Cancer Institute · National Heart, Lung, and Blood Institute · Foundation for the National Institutes of Health · National Institute of Biomedical Imaging and Bioengineering
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