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Sökning: onr:"swepub:oai:lup.lub.lu.se:9083cd32-4c24-455a-b3f1-80d78ae05bda" > Hybrid biosynthetic...

Hybrid biosynthetic gene therapy vector development and dual engineering capacity

Jones, Charles H (författare)
The State University of New York
Ravikrishnan, Anitha (författare)
The State University of New York
Chen, Mingfu (författare)
The State University of New York
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Reddinger, Ryan (författare)
The State University of New York
Kamal Ahmadi, Mahmoud (författare)
The State University of New York
Rane, Snehal (författare)
The State University of New York
Hakansson, Anders P (författare)
Lund University,Lunds universitet,Experimentell infektionsmedicin, Malmö,Forskargrupper vid Lunds universitet,Experimental Infection Medicine, Malmö,Lund University Research Groups
Pfeifer, Blaine A (författare)
The State University of New York
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 (creator_code:org_t)
2014-08-11
2014
Engelska 6 s.
Ingår i: Proceedings of the National Academy of Sciences. - : Proceedings of the National Academy of Sciences. - 1091-6490 .- 0027-8424. ; 111:34, s. 5-12360
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Genetic vaccines offer a treatment opportunity based upon successful gene delivery to specific immune cell modulators. Driving the process is the vector chosen for gene cargo packaging and subsequent delivery to antigen-presenting cells (APCs) capable of triggering an immune cascade. As such, the delivery process must successfully navigate a series of requirements and obstacles associated with the chosen vector and target cell. In this work, we present the development and assessment of a hybrid gene delivery vector containing biological and biomaterial components. Each component was chosen to design and engineer gene delivery separately in a complimentary and fundamentally distinct fashion. A bacterial (Escherichia coli) inner core and a biomaterial [poly(beta-amino ester)]-coated outer surface allowed the simultaneous application of molecular biology and polymer chemistry to address barriers associated with APC gene delivery, which include cellular uptake and internalization, phagosomal escape, and intracellular cargo concentration. The approach combined and synergized normally disparate vector properties and tools, resulting in increased in vitro gene delivery beyond individual vector components or commercially available transfection agents. Furthermore, the hybrid device demonstrated a strong, efficient, and safe in vivo humoral immune response compared with traditional forms of antigen delivery. In summary, the flexibility, diversity, and potential of the hybrid design were developed and featured in this work as a platform for multivariate engineering at the vector and cellular scales for new applications in gene delivery immunotherapy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Nyckelord

Animals
Antigen-Presenting Cells
Cell Line
Escherichia coli
Female
Gene Transfer Techniques
Genetic Engineering
Genetic Therapy
Genetic Vectors
Immunization
Mice
Mice, Inbred BALB C
Models, Animal
Ovalbumin
Vaccines, DNA

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