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Thomas C. Luke

Researcher at Naval Medical Research Center

Publications -  39
Citations -  3190

Thomas C. Luke is an academic researcher from Naval Medical Research Center. The author has contributed to research in topics: Antibody & Virus. The author has an hindex of 17, co-authored 35 publications receiving 2860 citations. Previous affiliations of Thomas C. Luke include Silver Spring Networks & Henry M. Jackson Foundation for the Advancement of Military Medicine.

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Protection of human ACE2 transgenic Syrian hamsters from SARS CoV-2 variants by human polyclonal IgG from hyper-immunized transchromosomic bovines

TL;DR: In this paper, the authors used fully human polyclonal human IgG (SAB-185), derived from hyperimmunization of transchromosomic bovines with DNA plasmids encoding the SARS-CoV-2 Wa-1 strain S protein or purified ectodomain of S protein.
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A dengue DNA vaccine formulated with Vaxfectin® is well tolerated, and elicits strong neutralizing antibody responses to all four dengue serotypes in New Zealand white rabbits

TL;DR: The formulated vaccine and the adjuvant were tested for safety and/or immunogenicity in New Zealand white rabbits using a repeat dose toxicology study and were found to be well tolerated by the animals.
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Dengue virus photo-inactivated in presence of 1,5-iodonaphthylazide (INA) or AMT, a psoralen compound (4′-aminomethyl-trioxsalen) is highly immunogenic in mice

TL;DR: Two novel methods of dengue virus inactivation using iodonaphthyl azide and aminomethyl trioxsalen were compared with traditional virus in activation by formaldehyde, and only mice vaccinated with AMT inactivated virus mounted T cell responses similar to live, uninactivated virus.
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Human immunoglobulin from transchromosomic bovines hyperimmunized with SARS-CoV-2 spike antigen efficiently neutralizes viral variants.

TL;DR: In this article, a polyclonal, fully human, anti-SARS-CoV-2 immunoglobulin produced in transchromosomic bovines was hyperimmunized with two doses of plasmid DNA encoding the SARS CoV 2 Wuhan strain S gene, followed by repeated immunization with spike protein purified from insect cells.
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Full-Genome Sequence of Human Betacoronavirus 2c Jordan-N3/2012 after Serial Passage in Mammalian Cells

TL;DR: The full genome sequence of the Jordan-N3/2012 strain after serial passage in two distinct mammalian cell lines exhibits noteworthy stability, which may inform the development of vaccines and therapeutics used to treat infection with this virus.