Completed Infection & Immunity Cancer

Development of a universal HIV-1 vaccine

In plain English

AI plain-English summary

A single injection could train the immune system to recognise and attack the parts of HIV that the virus cannot afford to change. HIV’s extraordinary ability to mutate has made it nearly impossible to design a vaccine that works against all circulating strains. The virus’s surface proteins shift constantly, allowing it to evade antibodies. But some regions of those proteins must stay stable for the virus to survive. This candidate vaccine deliberately targets those conserved regions, forcing the immune system to focus on the virus’s weak points rather than chasing its ever-changing disguise. If this small pilot study in healthy volunteers in Oxford shows that the approach is safe and provokes the right immune response, it would justify moving to larger, more expensive trials. A successful universal HIV vaccine would transform the fight against a pandemic that continues to spread largely unchecked. It would not cure people already infected, but it could prevent new infections on a global scale, reducing the need for lifelong antiretroviral therapy and shifting the trajectory of the epidemic. For now, the work remains at an early, fundamental stage—testing a concept that has never been tried in humans.

View original technical description
HIV infection and AIDS continues to spread in a virtually uncontrolled manner. The best and possibly only hope to change this alarming situation is a safe, effective, accessible protective vaccine. Arguably the biggest challenge in developing such a vaccine is the enormous HIV variability, which dwarfs almost any other infection. However, all parts of the virus cannot easily change. To remain alive, HIV has to keep some smaller regions of its proteins more or less constant. We have taken an advantage of this and constructed a simple candidate vaccine designed specifically to overcome the HIV variability by focusing the body defences on the conserved viral parts. Here, we are proposing to test this approach for the first time in a small pilot study in healthy individuals in Oxford. Successful outcome of this study would strongly support further evaluation of this vaccination strategy in larger and more expensive clinical studies.

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Researchers

Lucy Dorrell (Co-Investigator)Tomas Hanke (Principal Investigator)

Related Research

Grants with similar aims, by meaning.

A universal T cell vaccine for HIV-1
Definition and induction of broadly protective responses against HIV-1
Humoral immunity to Human Immunodeficiency Virus (HIV)
European AIDS Vaccine Initiative 2020
Structure-based vaccine design: using structural information from HIV-2 to design better HIV-1 immunogens

Original classification

Research Grant

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