The 2022 mpox outbreak prompted scientists to search for targeted and more practical interventions. Vaccines for smallpox were reused during the outbreak, but those vaccines are complex and costly to produce. Researchers in Italy first isolated twelve antibodies from the blood of people who had been infected with MPXV or vaccinated, yet the exact viral binding sites were unknown.
A team at The University of Texas at Austin then applied the AlphaFold 3 AI model to predict which of roughly 35 proteins on the virus surface the antibodies bind to. AlphaFold 3 predicted with high confidence that several antibodies target a surface protein called OPG153, and follow-up laboratory experiments verified that prediction.
When mice were injected with an engineered form of OPG153, they produced antibodies that neutralized MPXV. UT researcher Jason McLellan, a co-lead author, called the work unexpected because OPG153 had not been considered before as a vaccine or drug target. The team describes the method as reverse vaccinology: they began with survivor antibodies, identified the viral target, and engineered an antigen to elicit a similar response. The discovery could support a vaccine antigen or antibody therapies that are cheaper and easier to make than whole-virus vaccines. UT Austin and an Italian foundation have filed patent applications, and the work received partial funding from the Welch Foundation.
Difficult words
- outbreak — A sudden increase in disease cases.
- isolate — To obtain a specific substance or organism.isolated
- antibody — A protein made by the immune system.antibodies
- neutralize — To stop a virus from infecting cells.neutralized
- engineer — To design or create something deliberately.engineered
- antigen — A substance that triggers an immune response.
- reverse vaccinology — Starting with antibodies to find vaccine targets.
Tip: hover, focus or tap highlighted words in the article to see quick definitions while you read or listen.
Discussion questions
- What are the possible benefits of designing a vaccine antigen instead of using whole-virus vaccines?
- How could tools like AlphaFold 3 change the speed and cost of vaccine development?
- What ethical or practical issues might arise when patenting vaccine targets discovered from patient antibodies?
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