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Immunomodulation in type 1 diabetes by NBI-6024, an altered peptide ligand of the insulin B(9-23) epitope

  • D. G. Alleva
  • , R. A. Maki
  • , A. L. Putnam
  • , J. M. Robinson
  • , M. S. Kipnes
  • , P. Dandona
  • , J. B. Marks
  • , D. L. Simmons
  • , C. J. Greenbaum
  • , R. G. Jimenez
  • , P. J. Conlon
  • , P. A. Gottlieb
  • Neurocrine Biosciences Incorporated
  • University of Colorado Anschutz Medical Campus
  • Diabetes and Glandular Disease Clinic
  • University of Miami
  • Department of Veterans Affairs
  • Virginia Mason Medical Center

Research output: Contribution to journalArticlepeer-review

69 Scopus citations

Abstract

NBI-6024 is an altered peptide ligand (APL) corresponding to the 9-23 amino acid region of the insulin B chain (B(9-23)), an epitope recognized by inflammatory interferon-γ-producing T helper (Th)1 lymphocytes in type 1 diabetic patients. Immunomodulatory effects of NBI-6024 administration in recent-onset diabetic patients in a phase I clinical trial (NBI-6024-0003) were measured in peripheral blood mononuclear cells using the enzyme-linked immunosorbent spot assay. Analysis of the mean magnitude of cytokine responses to B(9-23) and NBI-6024 for each cohort showed significant increases in interleukin-5 responses (a Th2 regulatory phenotype) in cohorts that received APL relative to those receiving placebo. A responder analysis showed that Th1 responses to B(9-23) and NBI-6024 were observed almost exclusively in the placebo-treated diabetic population but not in nondiabetic control subjects and that APL administration (five biweekly subcutaneous injections) significantly and dose-dependently reduced the percentage of patients with these Th1 responses. The results of this phase I clinical study strongly suggest that NBI-6024 treatment shifted the Th1 pathogenic responses in recent-onset type 1 diabetic patients to a protective Th2 regulatory phenotype. The significance of these findings on the clinical outcome of disease is currently under investigation in a phase II multidose study.

Original languageEnglish
Pages (from-to)59-69
Number of pages11
JournalScandinavian Journal of Immunology
Volume63
Issue number1
DOIs
StatePublished - Jan 2006

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