NIH-funded research R01 grant

Vaccine study in mice to protect against gonorrhea using a new OMV-based approach

Official title: Transgenic mouse models of disease to test an innovative OMV-based vaccine for protection against the pathogenic Neisseriae

Funded at Georgia State University · NIH-11593936 · Data updated 2026-11-12

Researchers are testing an OMV-based vaccine in mouse models to block Neisseria gonorrhoeae infection by targeting key bacterial proteins.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionGeorgia State University
NIH-funded
Lab location1 site (Atlanta, United States)
Project startSeptember 24, 2025
Project endAugust 31, 2030
Funding year2026
Award (this year)$300,744
NIH project number3R01AI192648-02S1
Project IDNIH-11593936 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are individuals at risk for gonorrhea infections, including sexually active adults, who would later be eligible for vaccine trials.

Less likely to help

Patients with existing hard-to-treat infections or those outside vaccine trial criteria may not directly benefit.

What this research studies

This grant supports studies in transgenic mouse models to test a novel vaccine strategy against the human-specific pathogen Neisseria gonorrhoeae. The approach focuses on outer membrane transport proteins that are essential for the bacteria during infection and are targeted by antibodies to hinder growth and promote bacterial killing. By using OMV-based vaccines that present binding-defective forms of these proteins, the work aims to generate protective immune responses in vivo. The project includes creating and evaluating vaccine candidates for safety and efficacy in relevant animal models over several years. The ultimate goal is to move toward a vaccine option that could reduce gonorrhea infections and their complications in people.

Why it matters

Potential benefit: If successful, this vaccine approach could reduce gonorrhea infections and prevent complications such as pelvic inflammatory disease and infertility.

How similar studies have gone: Preclinical models have shown that OMV-based vaccines can elicit protective antibodies against surface bacterial proteins, supporting further development.

Where this research is happening

  • Georgia State University
    Atlanta, United States
    Active

Researchers

  • Principal investigator: Cornelissen, Cynthia N — Georgia State University
  • Study coordinator: Cornelissen, Cynthia N

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.