Jiayuan Kong, Kailei D Goodier, Kedar Krishnan, Christian Hopkins, Chi Zhang, Jessica L Stelzel, Evan Wang, Hexiang Feng, Yueh-Hsun Yang, Minh Phan, Zhi-Cheng Yao, Joshua C Doloff, Hai-Quan Mao, Sashank K Reddy
Radiation dermatitis (RD) is a debilitating side effect of radiation therapy, affecting nearly 95% of irradiated cancer patients, yet no FDA-approved therapies exist. Here, we introduce a nanofiber-hydrogel composite (NHC) matrix loaded with adipose-derived stem cell extracellular vesicles (ADSC-EVs), enabling sustained host cell recruitment and EV release in vivo. A single subcutaneous injection following ionizing radiation prevents functional and histological sequelae of radiation damage, whereas bolus EVs or NHC alone do not. Treated skin regenerates near-normal epidermal and dermal architecture with preservation of dermal appendages. Mechanistically, NHC modulates local inflammation by promoting pro-regenerative macrophage polarization and reducing pro-fibrotic fibroblast differentiation, while sustained EV delivery enhances angiogenesis, hair follicle regrowth, and neo-follicle formation. Pathway analysis indicates that NHC primarily modulates IL-17-associated inflammatory signaling, whereas EVs activate Relaxin and PI3K-Akt pathways linked to tissue regeneration. Together, NHC and EVs synergistically remodel irradiated tissue and represent a practical, off-the-shelf therapeutic strategy for RD.