Cutaneous suction-mediated transfection in mice for delivery of DNA-encoded vaccines and proteins
Lallow, E. O.; Brandtjen, I.; Mo, Y.; Gulley, M.; Osorio, L.; Kudchodkar, S.; Jhumur, N. C.; Roberts, C. C.; Denzin, L. K.; Shreiber, D. I.; Parekkadan, B.; Lin, H.; Maslow, J. N.
Show abstract
An important step to fulfill the functionalities of DNA vaccines and therapeutics is transfection in vivo to produce the encoded antigens or therapeutic proteins. A cutaneous suction-based method has demonstrated effectiveness in many animal models and has been successfully applied in human clinical trials, but has not been extended to mouse models, where numerous disease models, transgenic strains, and murine-specific reagents exist. The current work establishes and optimizes methods for cutaneous suction-mediated DNA transfection in mice. By adapting a smaller cup diameter and smaller injection volume, the challenges of skin hyperelasticity and decreased skin thickness can be effectively addressed, and vaccinating mice with the GLS-5310 SARS-CoV-2 DNA vaccine yielded high levels of binding antibody and T cell responses. Additionally, suction following injection of a novel pVAX1-based expression vector yielded systemic levels of a SEAP transgene. Thus, suction-mediated delivery of nucleic acid-based therapies and vaccines can be a valuable tool for the study in pre-clinical mouse models.
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