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- URN to cite this document:
- urn:nbn:de:bvb:355-epub-542611
- DOI to cite this document:
- 10.5283/epub.54261
Abstract
Inflammation and immune system activation are key pathologic events in the onset and escalation of diabetic retinopathy (DR). Both are driven by cytokines and complement originating from the retinal pigment epithelium (RPE). Despite the RPE’s pivotal role, there is no therapeutic tool to specifically interfere with the RPE-related pathomechanism. A therapy that addresses RPE cells and counteracts ...

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