Recombinant Hepatitis B vaccine (1986)
Merck developed Recombivax HB, the first vaccine to use recombinant DNA technology — producing a viral protein in yeast cells rather than using blood-derived material. The approach eliminated the contamination risks of earlier plasma-derived hepatitis B vaccines and demonstrated that targeted protein engineering could replace crude whole-pathogen approaches.
Universal infant hepatitis B vaccination was adopted in the United States by 1991 and globally through WHO recommendations.
The recombinant platform became the foundation for subsequent precision vaccines, including HPV vaccines, and proved that targeting a single protein could provide effective immunity.
Liu's selective peptide vaccine follows the same philosophical arc: rather than targeting the whole bacterium, it isolates one specific protein variant. The recombinant hepatitis B vaccine proved this precision approach could work at scale.
