Drug intelligence / Profile preview

p24CE + p55gag + IL-12 + MVA62B + bNAbs

Development stage
Unknown
Lead developer
University of California, San Francisco
Modality
Oncolytic Viruses → Oncolytic Therapeutics, DNA Vaccines → Plasmid DNA → DNA Therapeutics → Nucleic Acid Therapeutics, Prophylactic Vaccines → Vaccines & Immunotherapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics, Cytokines & Interferons → Recombinant Proteins and Enzymes
Administration
Intramuscular, Intravenous
01

Overview

This experimental combinatorial HIV therapeutic regimen is being developed through a collaboration between the **University of California, San Francisco (UCSF)** and **Ichor Medical Systems**. The regimen utilizes a multi-modal "prime-boost" strategy combined with passive immunotherapy to achieve HIV remission or a functional cure. It consists of DNA vaccines encoding the HIV conserved element **p24 (p24CE)** and **p55gag** antigens, delivered via electroporation (likely using Ichor's TriGrid system). An **interleukin-12 (IL-12)** plasmid DNA serves as a molecular adjuvant to enhance cellular immune responses. This is followed by a boost with the **MVA62B** viral vector (Modified Vaccinia Ankara). Additionally, the regimen incorporates **broadly neutralizing antibodies (bNAbs)** to provide passive immunity, neutralize circulating virus, and potentially clear infected cells. The p24CE component is specifically designed to focus the immune response on highly conserved viral regions to prevent immune escape.

Other names
p24CE + interleukin-12 + p55gag + MVA62B + broadly neutralizing antibodiesUCSF HIV therapeutic vaccine regimen
02

Targets

IL-12R (Interleukin-12 receptor)gp41 (Human immunodeficiency virus type 1 glycoprotein 41)HIV-1 antigensp24 (HIV-1 capsid protein p24)

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