Enzyme-Responsive DNA Origami-Antibody Conjugates for Targeted and Combined Therapy of Choroidal Neovascularization.
Yuqi WuXuan QinXing LuChen JiYufan LingJiawei ZhangHaoliang ShiBinbin ChuBin SongHouyu WangYao HePublished in: ACS nano (2024)
Monotherapy, especially the use of antibodies targeting vascular endothelial growth factor (VEGF), has shown limitations in treating choroidal neovascularization (CNV) since reactive oxygen species (ROS) also exacerbate CNV formation. Herein, we developed a combination therapy based on a DNA origami platform targeting multiple components of ocular neovascularization. Our study demonstrated that ocular neovascularization was markedly suppressed by intravitreal injection of a rectangular DNA origami sheet modified with VEGF aptamers (Ap) conjugated to an anti-VEGF antibody (aV) via matrix metalloproteinase (MMP)-cleavable peptide linkers in a mouse model of CNV. Typically, the DNA origami-based therapeutic platform selectively accumulates in neovascularization lesions owing to the dual-targeting ability of the aV and Ap, followed by the cleavage of the peptide linker by MMPs to release the antibody. Together, the released antibody and Ap inhibited VEGF activity. Moreover, the residual bare DNA origami could effectively scavenge ROS, reducing oxidative stress at CNV sites and thus maximizing the synergistic effects of inhibiting neovascularization.
Keyphrases
- vascular endothelial growth factor
- cancer therapy
- combination therapy
- circulating tumor
- reactive oxygen species
- endothelial cells
- cell free
- single molecule
- oxidative stress
- mouse model
- transcription factor
- drug delivery
- dna damage
- nucleic acid
- optical coherence tomography
- cell death
- high throughput
- optic nerve
- stem cells
- signaling pathway
- randomized controlled trial
- clinical trial
- photodynamic therapy
- open label
- age related macular degeneration
- ultrasound guided
- replacement therapy
- cell migration