Pharmacodynamics of anti-HIV gene therapy using viral vectors and targeted endonucleases
Author(s) -
Pavitra Roychoudhury,
Harshana S. De Silva Feelixge,
Harlan L. Pietz,
Daniel Stone,
Keith R. Jerome,
Joshua T. Schiffer
Publication year - 2016
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkw104
Subject(s) - transduction (biophysics) , reporter gene , transgene , biology , computational biology , genetic enhancement , gene , viral vector , vectors in gene therapy , vector (molecular biology) , gene delivery , gene expression , expression cassette , genetics , recombinant dna , biochemistry
A promising curative approach for HIV is to use designer endonucleases that bind and cleave specific target sequences within latent genomes, resulting in mutations that render the virus replication incompetent. We developed a mathematical model to describe the expression and activity of endonucleases delivered to HIV-infected cells using engineered viral vectors in order to guide dose selection and predict therapeutic outcomes.
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