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A novel class of self-complementary AAV vectors with multiple advantages based on cceAAV lacking mutant ITR.
Zhang, Junping; Frabutt, Dylan A; Chrzanowski, Matthew; Li, Ning; Miller, Lohra M; Tian, Jiahe; Mulcrone, Patrick L; Lam, Anh K; Draper, Benjamin E; Jarrold, Martin F; Herzog, Roland W; Xiao, Weidong.
Afiliación
  • Zhang J; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Frabutt DA; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Chrzanowski M; Nikegen LLC, Wynnewood, PA 19096, USA.
  • Li N; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Miller LM; Megadalton Solutions, Bloomington, IN 47401, USA.
  • Tian J; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
  • Mulcrone PL; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Lam AK; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Draper BE; Megadalton Solutions, Bloomington, IN 47401, USA.
  • Jarrold MF; Chemistry Department, Indiana University, Bloomington, IN 47405, USA.
  • Herzog RW; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
  • Xiao W; Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
Mol Ther Methods Clin Dev ; 32(1): 101206, 2024 Mar 14.
Article en En | MEDLINE | ID: mdl-38390555
ABSTRACT
Self-complementary AAV vectors (scAAV) use a mutant inverted terminal repeat (mITR) for efficient packaging of complementary stranded DNA, enabling rapid transgene expression. However, inefficient resolution at the mITR leads to the packaging of monomeric or subgenomic AAV genomes. These noncanonical particles reduce transgene expression and may affect the safety of gene transfer. To address these issues, we have developed a novel class of scAAV vectors called covalently closed-end double-stranded AAV (cceAAV) that eliminate the mITR resolution step during production. Instead of using a mutant ITR, we used a 56-bp recognition sequence of protelomerase (TelN) to covalently join the top and bottom strands, allowing the vector to be generated with just a single ITR. To produce cceAAV vectors, the vector plasmid is initially digested with TelN, purified, and then subjected to a standard triple-plasmid transfection protocol followed by traditional AAV vector purification procedures. Such cceAAV vectors demonstrate yields comparable to scAAV vectors. Notably, we observed enhanced transgene expression as compared to traditional scAAV vectors. The treatment of mice with hemophilia B with cceAAV-FIX resulted in significantly enhanced long-term FIX expression. The cceAAV vectors hold several advantages over scAAV vectors, potentially leading to the development of improved human gene therapy drugs.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Ther Methods Clin Dev Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos