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Combination Intervention-University of California, San Francisco-HIV infection

Development stage
Unknown
Lead developer
University of California, San Francisco
Modality
Small Molecules, DNA Vaccines → Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Viral Vector Vaccines → Recombinant Vaccines → Prophylactic Vaccines → Vaccines & Immunotherapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intramuscular, Intravenous, Subcutaneous
01

Overview

This multi-component combination immunotherapy regimen is being developed by the University of California, San Francisco (UCSF) to induce sustained HIV remission (functional cure) in individuals living with HIV. The intervention follows a multi-stage 'prime-boost-kill' strategy designed to enhance HIV-specific T cell responses and neutralize the viral reservoir. The regimen consists of: (1) therapeutic vaccination with a DNA vaccine targeting conserved elements (CE) of the HIV Gag protein (p24CE) adjuvanted with Interleukin-12 (IL-12); (2) a viral vector boost using Modified Vaccinia Ankara (MVA/HIV62B); (3) administration of two broadly neutralizing antibodies (bNAbs), 10-1074 (targeting the V3 loop) and VRC07-523LS (targeting the CD4 binding site); and (4) lefitolimod, a Toll-like receptor 9 (TLR9) agonist acting as an innate immune stimulator. This combinatorial approach aims to achieve post-intervention control of HIV after the analytical interruption of antiretroviral therapy (ART).

Other names
UCSF HIV Remission Combination Therapyp24CE/IL-12 + MVA62B + 10-1074 + VRC07-523LS + lefitolimod
02

Targets

TLR9 (Toll-like receptor 9)Env (HIV-1 envelope glycoprotein)Gag (HIV-1 Gag polyprotein)

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