High-Dose Oral Insulin in Young Children at High Risk for Type 1 Diabetes: The Pre-POInT-early Clinical Trial
Assfalg, R.; Knoop, J.; Hoffman, K.; Pfirrmann, M.; Zapardiel-Gonzalo, J. M.; Hofelich, A.; Eugster, A.; Weigelt, M.; Matzke, C.; Reinhardt, J.; Fuchs, Y.; Bunk, M.; Weiss, A.; Hippich, M.; Halfter, K.; Hauck, S.; Hasford, J.; Achenbach, P.; Bonifacio, E.; Ziegler, A. G.
Show abstract
BackgroundOral administration of antigen can induce immunological tolerance. Insulin is a key autoantigen in childhood type 1 diabetes with insulin autoimmunity often appearing in the first years of life. Here, oral insulin was given as antigen-specific immunotherapy before the onset of autoimmunity in children from age 6 months to assess its safety and actions on immunity and the gut microbiome. MethodsA phase I/II randomized controlled trial was performed in 44 islet autoantibody-negative children aged 6 months to 2 years with genetic risk for type 1 diabetes. Children were randomized 1:1 to daily oral insulin (7.5 mg with dose escalation to 67.5 mg) or placebo for 12 months. Primary outcome was safety and immune efficacy pre-specified as hypoglycemia and induction of antibody or T cell responses to insulin, respectively. ResultsOral insulin was well tolerated with no changes in metabolic variables. Immune responses to insulin were observed in both children who received insulin (55%) and placebo (67%), and were modified by the INSULIN gene. Among children with type 1 diabetes-susceptible INSULIN genotype, antibody responses to insulin were more frequent in insulin-treated (cumulative response, 75.8%) as compared to placebo-treated children (18.2%; P=0.0085), and T cell responses to insulin were modified by treatment-independent inflammatory episodes. Changes in the microbiome were related to INSULIN genotype. ConclusionThe study demonstrated that oral insulin immunotherapy in young genetically at-risk children was safe and engaged the adaptive immune system in an INSULIN genotype-dependent manner, and linked inflammatory episodes to the activation of insulin-responsive T cells. Trial registrationClinicaltrials.gov NCT02547519 FundingGerman Center for Diabetes Research (DZD e.V.), Juvenile Diabetes Research Foundation (JDRF, grant 1-SRA-2018-546-S-B), Federal Ministry of Education and Research (BMBF, grant FKZ01KX1818).
Matching journals
The top 3 journals account for 50% of the predicted probability mass.