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Principal Investigator: Sun Young Lee
Organization: UNIVERSITY OF SOUTHERN CALIFORNIA
Fiscal Year: 2024
Award: $476,894
Funding agency: National Eye Institute
Abstract
Intravitreal injection of anti-vascular endothelial growth factor (VEGF) agent monotherapy is the current mainstay
for treating neovascular age-related macular degeneration (NVAMD). Despite its vision saving benefit, some
patients fail to respond to the treatment because of insufficient therapeutic effect and/or the socioeconomic
burden of frequently required repeat injections. Therefore, the long-term goal of our studies is to develop superior
or adjunctive approaches to the current anti-VEGF therapy that can provide active targeting of NVAMD, have
the capacity to deliver multiple drugs, and maintain long-term efficacy. Exosomes are naturally occurring, cell
secreted, and nano-sized extracellular vesicles. Exosomes carry various cargos including microRNAs, proteins,
and lipids for cell-to-cell communications. Recently, we have shown that intravitreally delivered ASL-exosomes
composed of Anchor, Spacer, and Arg-Gly-Asp acid (RGD) Ligand-modification actively target choroidal
neovascularization (CNV) with adequate retinal penetration. The unique nature of exosomes and our study
demonstrate great promise in exosomes as the next regeneration intraocular drug delivery system. However,
the accelerated translation to humans has been hindered due to a lack of clarity as to mechanisms of exosome
uptake within the retina thus preventing a standardized formulation and an optimized therapeutic application of
exosomes. The objective of the current studies is to elucidate the extracellular and intracellular mechanisms by
which ASL-exosomes actively target ocular NV and to use this information in optimizing this drug delivery system
for simultaneous delivery of Aflibercept and miR-24 to suppress ocular NV and its secondary fibrosis through
independent pathways. Our proposed studies will test the hypothesis that intravitreally delivered ASL-exosomes
allow their targeted delivery to ocular NV lesions through active binding to increasingly expressed
transmembrane integrins at NV sites and through increased intracellular uptake of exosomes by integrin
receptor-mediated intracellular endocytosis. Further, we hypothesize that the ASL-exosome system that is
complemented with active targeting and sustained multi-drug delivery capacity with minimal immune responses
can effectively suppress NV and fibrosis by co-delivering Aflibercept and miR-24, a new intracellular target for
retinal fibrosis. The central hypothesis will be tested by pursuing three specific aims. Aim 1 is to determine the
mechanism by which ASL-exosomes actively target ocular NV. Aim 2 is to optimize the formulation of multi-
drugs loaded ASL-exosomes. Aim 3 is to determine sustained multi-drug delivery using exosomes and related
immune responses. The research proposed in this application is innovative because the combination of an
exosome-based intraocular drug delivery system with active targeting is a novel strategy that has the potential
to change the current treatment paradigm from passive targeting-directed monotherapy to active targeting-
directed multi-drug delivery with sustained efficacy for the treatment of various retinal and choroidal vascular
diseases.
Terms: <Acceleration><Acids><Arg-Gly-Asp><Arginine-Glycine-Aspartic Acid Cell Adhesion Domain><Binding><Blindness><Blood Vessels><Caveolin Proteins><Caveolins><Cell Body><Cell Communication><Cell Interaction><Cell Line><Cell secretion><Cell-to-Cell Interaction><CellLine><Cells><Cellular Secretion><Choroid Neovascularization><Choroidal Neovascularization><Clathrin><Clinical><Combined Modality Therapy><Coupled><Development><Diabetic Retinopathy><Diffusion><Disciform macular degeneration><Disciform senile macular retinal degeneration><Drug Delivery><Drug Delivery Systems><Drugs><Economic Burden><Endocytosis><Endothelial Cells><Engineering><Exudative AMD><Exudative age-related macular degeneration><Eye diseases><Fibrosis><Formulation><Gliosis><Goals><Health Care Costs><Health Costs><Healthcare Costs><Histologic><Histologically><Human><Immune response><Immunologic Tests><Immunological Tests><Immunological response><In Vitro><Infection><Inflammation><Inflammatory Response><Injections><Integrins><Integrins Extracellular Matrix><Laser Electromagnetic><Laser Radiation><Lasers><Lesion><Ligands><Lipids><Mediating><Medication><Membrane><Mice><Mice Mammals><Micro RNA><MicroRNAs><Modeling><Modern Man><Modification><Molecular Interaction><Multimodal Therapy><Multimodal Treatment><Murine><Mus><Natural regeneration><Nature><Neovascular AMD><Neovascular age-related macular degeneration><Older Population><Pathologic><Pathway interactions><Patients><Penetration><Pharmaceutical Preparations><Physiologic><Physiological><Play><Process><Proteins><Public Health><RGD (sequence)><RGD Cell Adhesion Domain><RGD Domain><RGD Motif><RGD Tripeptide Sequence><RGD peptide><RGD tripeptide><Receptor Protein><Regeneration><Research><Retina><Retinal Degeneration><Retinal Vein Occlusion><Role><Sight><Site><Standardization><Strains Cell Lines><Subgroup><System><Testing><Therapeutic><Therapeutic Effect><Time><Toxic effect><Toxicities><Treatment Efficacy><Tube><VEGF><VEGFs><Vascular Diseases><Vascular Disorder><Vascular Endothelial Cell><Vascular Endothelial Growth Factors><Vision><Wet AMD><antagonism><antagonist><arginyl-glycyl-aspartic acid><blood vessel disorder><cell type><combination therapy><combined modality treatment><combined treatment><cultured cell line><degenerative retina diseases><developmental><diffused><diffuses><diffusing><diffusions><drug/agent><exosome><extracellular><extracellular vesicles><eye disorder><host response><immune system response><immunoresponse><innovate><innovation><innovative><intervention efficacy><intravitreal injection><membrane structure><miRNA><miRNAs><mouse model><multi-modal therapy><multi-modal treatment><murine model><nano sized><nanosized><new approaches><new therapeutic approach><new therapeutic intervention><new therapeutic strategies><new therapy approaches><new treatment approach><new treatment strategy><novel><novel approaches><novel strategies><novel strategy><novel therapeutic approach><novel therapeutic intervention><novel therapeutic strategies><novel therapy approach><ocular disease><ocular disorder><ocular neovascularization><older groups><older individuals><older person><ophthalmopathy><pathway><prevent><preventing><receptor><receptor mediated endocytosis><regenerate><retina degeneration><retinal angiogenesis><retinal degenerative><retinal degenerative diseases><site targeted delivery><social role><socio-economic><socio-economically><socioeconomically><socioeconomics><targeted delivery><therapeutic efficacy><therapy efficacy><translation to humans><uptake><vascular><vascular dysfunction><vasculopathy><vision loss><visual function><visual loss><wet form of AMD>