Therapy with the hsp60 peptide DiaPep277 in C-peptide positive type 1 diabetes patients


  • C. Mathieu, University Hospital St. Gasthuisberg, Leuven, Belgium; K. Decochez, Academic Hospital V.U.B., Brussels, Belgium; I. H. de Leeuw, C.E. de Block, University Hospital Antwerp, Edegem, Belgium; D. Nicolaij, O.L.V. Hospitaal, Kortrijk, Belgium; J. C. Daubresse, G. Krzentowski, Centre Hospitalier Universitaire, Charleroi/Jumet, Belgium; G. Lamberigts, University Hospital St. Jan, Brugge, Belgium; J. Tits, St. Jansziekenhuis, Genk, Belgium



Type 1 diabetes results from a T-cell mediated autoimmune destruction of insulin-producing pancreatic beta-cells. The 60-kDa heat-shock protein (hsp60) is one of the known target self-antigens. An immunogenic peptide from hsp60, p277, arrested beta-cell destruction and maintained insulin production in newly diabetic non-obese diabetic (NOD) mice. A randomized, double-blind, phase Ib/II study of peptide treatment was undertaken in recent onset type 1 diabetes patients with remaining insulin production.


Forty-eight recent onset type 1 diabetes patients were assigned subcutaneous injections of 0.2, 1.0 or 2.5 mg peptide DiaPep277 (n = 12 per dosage) at entry, and 1, 6 and 12 months, or four placebo injections (n = 12). The primary clinical endpoints were safety and efficacy (glucagon-stimulated C-peptide production at 6 and 12 months); secondary endpoints were HbA1c levels and daily insulin dose adjusted for body weight at 2, 6, 12 and 18 months.


C-peptide levels decreased over time in all groups except the 2.5 mg-treated. The decrease in C-peptide production was less in treated patients versus placebo, mostly in the 2.5 mg group. HbA1c increased significantly in the 1.0 mg group and in the 2.5 mg group at 2 and 18 months, respectively. No differences were seen in daily insulin doses. One patient was withdrawn from the study possibly owing to a treatment-related adverse event.


Multiple DiaPep277 peptide administration seems safe and may have a beneficial effect on C-peptide levels over time, but this finding is not supported by lower HbA1c levels or daily insulin requirement. Further investigation on a larger scale is warranted. Copyright © 2006 John Wiley & Sons, Ltd.