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In Vivo Production of Monoclonal Antibodies by Gene Transfer via Electroporation Protects against Lethal Influenza and Ebola Infections
Author(s) -
Chasity D. Andrews,
Yang Luo,
Ming Sun,
Jian Yu,
Arthur J. Goff,
Pamela J. Glass,
Neal N. Padte,
Yaoxing Huang,
David D. Ho
Publication year - 2017
Publication title -
molecular therapy — methods and clinical development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.285
H-Index - 32
ISSN - 2329-0501
DOI - 10.1016/j.omtm.2017.09.003
Subject(s) - electroporation , monoclonal antibody , virology , ebola virus , in vivo , dna vaccination , gene transfer , genetic enhancement , biology , antibody , gene , virus , immunology , immunization , microbiology and biotechnology , genetics
Monoclonal antibodies (mAbs) have wide clinical utility, but global access is limited by high costs and impracticalities associated with repeated passive administration. Here, we describe an optimized electroporation-based DNA gene transfer platform technology that can be utilized for production of functional mAbs in vivo, with the potential to reduce costs and administration burdens. We demonstrate that multiple mAbs can be simultaneously expressed at protective concentrations for a protracted period of time using DNA doses and electroporation conditions that are feasible clinically. The expressed mAbs could also protect mice against lethal influenza or Ebola virus challenges. Our findings suggest that this DNA gene transfer platform technology could be a game-changing advance that expands access to effective mAb therapeutics globally.

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