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CH505 mRNA-LNP HIV-1 vaccine is an investigational mRNA-based vaccine regimen designed to prevent HIV-1 infection. Developed by the Duke Human Vaccine Institute (DHVI) in collaboration with the National Institute of Allergy and Infectious Diseases (NIAID) and the University of Pennsylvania, the vaccine utilizes lipid nanoparticles (LNPs) to deliver nucleoside-modified messenger RNA encoding transmembrane-stabilized gp160 envelope (Env) trimers derived from the clade C CH505 transmitted-founder (TF) strain. The vaccine regimen, evaluated in the Phase 1 HVTN 312 clinical trial, employs a sequential priming and boosting strategy (using CH505M5 N197D mRNA-gp160 followed by CH505 TF mRNA-gp160 and CH505 w24 mRNA-gp160) to target and expand unmutated common ancestors (UCAs) of the CH235 lineage, guiding B-cell maturation toward the development of CD4-binding site (CD4bs) broadly neutralizing antibodies (bnAbs).
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