Microneedle-mediated Delivery of Immunomodulators Restores Immune Privilege in Hair Follicles and Reverses Immune-Mediated Alopecia.
Nour YounisNúria PuigmalAbdallah El KurdiAndrew BadaouiDongliang ZhangClaudia MoralesAnis SaadDiane CruzNadim Al RahyAndrea DaccacheTriana HuertaChrista DebanAhmad HalawiJohn ChoiPere DostaChristine LianNatalie ArtziJamil R AzziPublished in: Advanced materials (Deerfield Beach, Fla.) (2024)
Disorders in the regulatory arm of the adaptive immune system result in autoimmune-mediated diseases. While systemic immunosuppression is the prevailing approach to manage them, it fails to achieve long-lasting remission due to concomitant suppression of the regulatory arm and carries the risk of heightened susceptibility to infections and malignancies. Alopecia Areata is a condition characterized by localized hair loss due to autoimmunity. The accessibility of the skin provides an opportunity for local rather than systemic intervention to avoid broad immunosuppression. We hypothesized that expansion of endogenous regulatory T cells (T regs ) at the site of antigen encounter can restore the immune balance and generate a long-lasting tolerogenic response. We therefore utilized a hydrogel microneedle (MN) patch for delivery of CCL22, a chemoattractant for T regs , and IL-2, a T reg survival factor to amplify them. In an immune-mediated murine model of alopecia, we showed local bolstering of T reg numbers leading to sustained hair regrowth and attenuation of inflammatory pathways. In a humanized skin transplant mouse model, we confirmed expansion of T regs within human skin without engendering peripheral immunosuppression. The MN patch offered high-loading capacity and shelf-life stability for prospective clinical translation. By harmonizing immune responses locally, we aspire to reshape the landscape of autoimmune skin disease management. This article is protected by copyright. All rights reserved.
Keyphrases
- regulatory t cells
- dendritic cells
- wound healing
- soft tissue
- immune response
- mouse model
- multiple sclerosis
- drug induced
- randomized controlled trial
- transcription factor
- liver injury
- oxidative stress
- drug delivery
- room temperature
- toll like receptor
- transition metal
- disease activity
- rheumatoid arthritis
- monoclonal antibody
- inflammatory response