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The 'Combi 3 group' refers to a specific high-dose combination vaccine regimen evaluated in the Phase I ANRS VRI06 clinical trial (NCT04842682) for the prevention of HIV infection. This prophylactic strategy involves the co-administration of **CD40.HIVRI.Env**, a dendritic cell-targeting biologic consisting of a monoclonal antibody against the CD40 receptor fused to the HIV-1 Clade C ZM96 envelope antigen (gp140), and **DNA-HIV-PT123**, a DNA vaccine encoding multiple HIV-1 antigens including gp140, Gag, Pol, and Nef. The regimen is adjuvanted with **Poly-ICLC** (Hiltonol), a synthetic double-stranded RNA that acts as a Toll-like receptor 3 (TLR3) agonist to stimulate innate immune pathways and enhance the adaptive response. The 'Combi 3' designation specifically identifies the cohort receiving the 3.0 mg dose of the CD40-targeted fusion protein in combination with the DNA vaccine. Results from the trial indicated that the combination was safe and capable of inducing early and sustained anti-envelope cellular and humoral immune responses.
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