Safety of the use of gold nanoparticles conjugated with proinsulin peptide and administered by hollow microneedles as an immunotherapy in type 1 diabetes

Author:

Tatovic D1ORCID,McAteer M A2,Barry J2,Barrientos A2,Rodríguez Terradillos K2,Perera I2,Kochba E3,Levin Y3,Dul M4,Coulman S A4,Birchall J C4,von Ruhland C5,Howell A1,Stenson R1,Alhadj Ali M1,Luzio S D6,Dunseath G6,Cheung W Y6,Holland G7,May K8,Ingram J R9,Chowdhury M M U10,Wong F S1,Casas R11,Dayan C1,Ludvigsson J12

Affiliation:

1. Diabetes Research Group, Cardiff University School of Medicine , Cardiff , UK

2. Midatech Pharma PLC , Cardiff , UK

3. NanoPass Technologies Ltd. , Nes Ziona , Israel

4. School of Pharmacy and Pharmaceutical Sciences, Cardiff University , Cardiff , UK

5. Central Biotechnology Services, Cardiff University , Cardiff , UK

6. Diabetes Research Unit Cymru, Institute for Life Sciences, Swansea University , Swansea , UK

7. Swansea Trials Unit, Swansea University Medical School , Swansea , UK

8. Department of Cellular Pathology, University Hospital of Wales , Cardiff , UK

9. Division of Infection & Immunity, Cardiff University School of Medicine , Cardiff , UK

10. Welsh Institute of Dermatology, University Hospital of Wales , Cardiff , UK

11. Division of Pediatrics, Department of Biomedical and Clinical Sciences, Faculty of Medicine and Health Sciences, Linköping University , Linköping , Sweden

12. Division of Pediatrics, Department of Biomedical and Clinical Sciences, Faculty of Medicine and Health Sciences and Crown Princess Victoria Children´s Hospital, Linköping University , Linköping , Sweden

Abstract

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

Funder

The Enhanced Epidermal Antigen Specific Immunotherapy Against Type 1 Diabetes

European Commission under the Health Cooperation Work Programme of the 7th Framework Programme

Publisher

Oxford University Press (OUP)

Subject

General Medicine

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