Article
Author: Dayan, C  ; Levin, Y  ; Alhadj Ali, M  ; von Ruhland, C  ; Rodríguez Terradillos, K  ; Dul, M  ; Barry, J  ; Birchall, J C  ; Ludvigsson, J  ; Casas, R  ; Wong, F S  ; May, K  ; Kochba, E  ; Cheung, W Y  ; Stenson, R  ; Barrientos, A  ; Howell, A  ; Coulman, S A  ; Ingram, J R  ; Dunseath, G  ; Chowdhury, M M U  ; McAteer, M A  ; Holland, G  ; Luzio, S D  ; Perera, I  ; Tatovic, D 
Abstract:Antigen-specific immunotherapy is an immunomodulatory strategy for autoimmune diseases, such as type 1 diabetes, in which patients are treated with autoantigens to promote immune tolerance, stop autoimmune β-cell destruction and prevent permanent dependence on exogenous insulin. In this study, human proinsulin peptide C19-A3 (known for its positive safety profile) was conjugated to ultrasmall gold nanoparticles (GNPs), an attractive drug delivery platform due to the potential anti-inflammatory properties of gold. We hypothesised that microneedle intradermal delivery of C19-A3 GNP may improve peptide pharmacokinetics and induce tolerogenic immunomodulation and proceeded to evaluate its safety and feasibility in a first-in-human trial. Allowing for the limitation of the small number of participants, intradermal administration of C19-A3 GNP appears safe and well tolerated in participants with type 1 diabetes. The associated prolonged skin retention of C19-A3 GNP after intradermal administration offers a number of possibilities to enhance its tolerogenic potential, which should be explored in future studies