Drug intelligence / Profile preview

AAV-DC

Development stage
Preclinical
Modality
Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies, Viral Vectors → Gene Addition/Replacement → Gene Therapies
Administration
Intravenous, Intratumoral, Subcutaneous, Intradermal, Intralymphatic
01

Overview

AAV-DC refers to a dendritic cell therapy in which dendritic cells are transduced or modified using an adeno-associated virus (AAV) vector. Adeno-associated viruses (AAVs) are small, non-enveloped viruses from the Parvoviridae family, widely used as vectors for gene therapy due to their low pathogenicity and ability to deliver genetic material into both dividing and non-dividing cells[1][3][5]. In the context of "AAV-DC," this typically means that dendritic cells have been engineered ex vivo with an AAV vector carrying a therapeutic gene or antigen, then administered as a cellular immunotherapy—often for cancer or infectious disease indications. The mechanism of action involves the presentation of encoded antigens by the modified dendritic cells to activate T-cell mediated immune responses against target diseases.

02

Targets

KPNA2 (Karyopherin subunit alpha-2)PRR (Pattern recognition receptors)

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