Drug intelligence / Profile preview

albumin-hitchhiking nanobody-STING agonist

Development stage
Preclinical
Lead developer
Vanderbilt University
Modality
Nanobodies (VHH) → Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Intravenous, Parenteral
01

Overview

An albumin-hitchhiking nanobody-STING agonist conjugate is a modular cancer immunotherapy platform developed by researchers at Vanderbilt University. The platform consists of a llama-derived single-domain antibody (nanobody) that binds to endogenous serum albumin, covalently conjugated to a stimulator of interferon genes (STING) agonist payload. By hitchhiking on circulating albumin, the conjugate exhibits significantly extended circulation half-life and enhanced accumulation in the tumor microenvironment (TME). Once localized in the tumor, the STING agonist payload activates the STING pathway, promoting innate immune activation, increasing the infiltration of dendritic cells and inflammatory macrophages, and reversing TME-mediated immunosuppression. This approach has been shown to enhance the therapeutic efficacy of adoptive cell therapies (ACT) and immune checkpoint inhibitors in preclinical solid tumor models.

Other names
albumin-hitchhiking nanobody-STING agonist conjugatealbumin-hitchhiking nanobody-STING agonist conjugatesalbumin-hitchhiking nanobody–STING agonistnanobody-STING agonist
02

Targets

IRF3 (Interferon regulatory factor 3)NF-κBPDCD1 (Programmed cell death protein 1 receptor)CD274 (Programmed cell death protein 1 ligand 1)TBK1 (TANK binding kinase 1)

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