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NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASESNIH · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASESNIH

An R2 non-neuroinvasive herpes simplex virus type 2 vaccine

Smith, Gregory Allan (Contact)·THYREOS, INC, IL·2024–2026·COMPLETED
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INSTITUTION

THYREOS, INC, IL

PRINCIPAL INVESTIGATOR

Smith, Gregory Allan (Contact)

FUNDING

$704K

YEAR

2024

MOONBASE SCORE

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Abstract

PROJECT SUMMARY There is an unmet need for a herpes simplex virus (HSV) vaccine. We propose to develop a live-attenuated HSV-2 vaccine based on our R2 technology platform. R2 vaccines show unprecedented safety and efficacy in animal models, and offer antigenicity superior to subunit/mRNA and single-round vaccine designs. R2 vaccines are also the first live-attenuated alphaherpesvirus vaccines that lack neuroinvasive potential, and thereby are incapable of establishing life-long infections in the nervous system. In phase I of this fast-track STTR application, we propose to: (i) produce a HSV- 2 self-excising infectious clone of a low-passage clinical isolate, (ii) use the clone to produce a HSV-2 R2 recombinant, and (iii) characterize the R2 vaccine in culture side by side with our existing HSV-1 R2 vaccine candidate. In phase II, the HSV-2 R2 vaccine will be tested for safety, immunogenicity, and efficacy in mice and guinea pigs. This work will provide the foundation to advance product development to clinical trials.

NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASESR42Special Emphasis Panel[ZRG1-DCAI-U(11)]modelsexistingcandidatedevelopproduceguineaclinicalherpesvirusdesignsapplicationalphaherpesvirusdevelopmentinfectiousanimaloffertestedsuperiorantigenicity

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