Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Volume 30 Issue 3-4, April 2023

Cover Credit: Gene therapy for patients with advanced neovascular age-related macular degeneration has reached clinical trial phases by introducing sFLT01. htsFLT01 gene construct is a novel anti-angiogenic tool with promising improvements compared to existing treatments. The critical properties of htsFLT01 molecule were maintained in desired limits post hinge deletion process when compared to sFLT01 protein. While, hinge shrinkage led to increased flexibility, stability and safety profile and decreased antigenicity of the htsFLT01 molecule. The image shows confocal microscopy of retinal vasculature in P16 mice, 2 weeks after AAV2-htsFLT01 intravitreal delivery. The presence of isolectin-positive dots in htsFLT01 treated eyes was the result of attenuation and impaired vascular formation due to anti-angiogenic effects of htsFLT01 protein.

Perspective

Top of page ⤴

Review Article

Top of page ⤴

Article

Top of page ⤴

Comment

Top of page ⤴

Brief Communication

Top of page ⤴

Article

Top of page ⤴

Correction

Top of page ⤴

Search

Quick links