HLA‐associated inverse correlation between T cell and antibody responsiveness to islet autoantigen in recent‐onset insulin‐dependent diabetes mellitus

<jats:title>Abstract</jats:title><jats:p>Insulin‐dependent diabetes mellitus (IDDM) is a T cell‐dependent immune‐mediated disease. Recently, a novel islet cell antigen (ICA69) recognized by autoantibodies was described. We tested T cell responsiveness to ICA69 in peripheral blood of patients with recent onset IDDM (<jats:italic>n</jats:italic> = 46), patients with long‐standing IDDM (<jats:italic>n</jats:italic> = 44), non‐diabetic age‐matched, islet cell autoantibody‐ and glutamic acid decarboxylase (GAD)65 antibody‐negative first‐degree relatives of IDDM patients (<jats:italic>n</jats:italic> = 15) and rheumatoid arthritis patients (<jats:italic>n</jats:italic> = 22). T cell responsiveness was significantly higher in recent onset IDDM patients, compared to IDDM patients post‐disease onset, non‐diabetic first degree relatives and rheumatoid arthritis patients (<jats:italic>p</jats:italic> < 0.001). In responding IDDM patients a significant inverse correlation between T cell and autoantibody responsiveness to ICA69 was observed (<jats:italic>p</jats:italic> < 0.0005). Immunogenetic evaluation revealed an association of HLA‐DR3 with T cell responsiveness to ICA69 (<jats:italic>p</jats:italic> < 0.02) and absence of ICA69‐reactive autoantibodies (<jats:italic>p</jats:italic> < 0.04). The increased T cell reactivity to ICA69 in the absence of antibody reactivity at onset of IDMM is associated with an HLA class II immune response gene, and therefore suggestive of a genetically controlled selective activation of T helper subsets to a specific autoantigen in humans.</jats:p>