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The HIV V1V2 mRNA-LNP vaccine is a preclinical lipid nanoparticle-encapsulated mRNA (mRNA-LNP) vaccine candidate designed to prevent HIV-1 infection. Developed through a collaboration involving the Icahn School of Medicine at Mount Sinai, the University of Pennsylvania, Oregon Health and Science University, and Acuitas Therapeutics, the vaccine encodes the V1V2 domain of the CRF_01.AE244 strain of the HIV-1 envelope glycoprotein gp120 on a trimeric 2J9C scaffold. The V1V2 domain is a key target for antibodies associated with a reduced risk of HIV-1 infection. Preclinical evaluations in mice and rhesus macaques have demonstrated that the vaccine is highly immunogenic, eliciting robust, cross-clade functional antibody responses capable of recognizing native envelope proteins and mediating Fc-dependent effector functions, such as antibody-dependent cellular phagocytosis (ADCP).
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