When antibodies backfire: Scientists uncover how imbalanced antibodies can protect gonorrhoea

New research reveals how some immune responses shield gonorrhoea bacteria from attack, offering crucial insights for developing an effective vaccine.

3D rendered image of Gonorrhoea bacterium - Neisseria gonorrhoeae

Scientists have recently discovered that an imbalance in immune proteins allows gonorrhoea to evade the body's defences in 3% of infections — a finding that could transform vaccine development for this global health threat, that is increasingly becoming resistant to antibiotics. 

Gonorrhoea, caused by the bacterium Neisseria gonorrhoeae, is the second most common bacterial sexually transmitted infection worldwide, with over 82 million cases in 2020. Whilst symptoms in men with urethral infections were significantly more common, research found that women who had the infection also lead to serious health  complications, such as ectopic pregnancy and infertility. 

Dr Samantha McKeand, Dr Amanda Rossiter-Pearson and researchers from the University of Birmingham, in collaboration with colleagues at the University of Oxford, have uncovered a surprising immune system paradox: in some people, antibodies designed to fight gonorrhoea actually protect the bacteria from being destroyed.

The research, published 30th January 2026 in mBio, examined bacterial samples and blood from 283 people with gonorrhoea infections as part of the G-ToG clinical trial. They found that approximately 3% of patients produced "blocking antibodies" that prevented their immune system from killing the bacteria. The key was not simply having too many antibodies, but rather an imbalance between two specific types: IgG2 and IgG3, which stick to the surface of the bacteria.

While IgG3 normally helps the immune system kill N. gonorrhoeae, high levels of IgG2 can interfere with this process. When IgG2 binds in greater amounts, it prevents IgG3 from triggering the bacterial killing mechanism, effectively allowing the bacteria to evade the body’s defences.

Although there is still no licensed gonorrhoea vaccine following a century of research, a meningitis vaccine tested in New Zealand unintentionally reduced gonorrhoea rates by approximately 30%, proving that vaccine protection is possible. But to create a targeted gonorrhoea vaccine, researchers need to ensure it stimulates the right type of immune response.

Our study shows that a very small number of people produce antibodies that unintentionally protect gonorrhoea bacteria rather than eliminate them.

Dr Amanda Rossiter-Pearson, Assistant Professor in Prokaryotic Infection Biology, University of Birmingham

Speaking about the latest findings, Dr Rossiter-Pearson says: “Our study shows that a very small number of people produce antibodies that unintentionally protect gonorrhoea bacteria rather than eliminate them. For a vaccine to work effectively, we need to include components that trigger IgG3 production rather than IgG2. This gives us a measurable target — we can test whether candidate vaccines are producing the right antibody balance to kill the bacteria rather than protect it."

With antibiotic resistance in gonorrhoea continuing to rise globally, the development of an effective vaccine is increasingly critical. Following on from this study, researchers can now begin refining OMV‑based vaccine candidates to favour beneficial IgG3 responses that harness the immune system's bacteria-killing power while avoiding the pitfalls that have derailed previous attempts over the last 100 years.