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Synthetic Biology Approaches for Engineering Next-Generation Adenoviral Gene Therapies

期刊

ACS NANO
卷 15, 期 9, 页码 13970-13979

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.1c04556

关键词

adenovirus; CRISPR; gene therapy; genetic circuits; protein engineering; synthetic biology; viral capsids; viral tropisms

资金

  1. National Institutes of Health [R01 CA211096-04, R01 EB026468-03, UG3 TR002851-02, T32 HL007317-43]

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Synthetic biology focuses on designing and assembling biological parts to construct artificial biological systems, leading to advances in diverse fields like neuroscience, cell-based therapies, and chemical manufacturing; gene therapy has made significant progress in proof-of-concept studies and clinical applications, with adenovirus showing increasing interest as a viral vector for gene therapy.
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.

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