Th1 and Th2 cell responses of type 1 diabetes patients and healthy controls to human heat-shock protein 60 peptides AA437-460 and AA394-408

Inflamm Res. 2005 Oct;54(10):415-9. doi: 10.1007/s00011-005-1362-9.

Abstract

Rationale: Type 1 diabetes mellitus (T1) is considered to be an immune mediated disease. Based on previous findings it might be suggested that heat shock protein 60 (Hsp60) could be involved in the mediation of the development of the disease. Furthermore a bias toward Th1 immune response was observed in T1D patients where the level of Th1 cytokines was elevated, while the level of Th2 was decreased.

Aim of the study: To determine Th1 (IFN-gamma) and Th2 (IL-13) cytokine levels in T1 diabetic and control subjects as well as to determine whether there is a shift towards Th1 or Th2 immune response.

Materials and methods: ELISPOT (Enzyme-linked ImmunoSPOT) analysis was employed to differentiate antigen specific T-cell responses of a Th1 (IFN-gamma) or Th2 (IL-13) type. 11 T1 diabetic patients and 9 healthy controls were investigated. For T-cell stimulation, we used a polyclonal mitogen or Tetanus toxoid (TT) as positive controls and two peptide antigens Hsp60 AA394-408 and Hsp60 AA437-460.

Results: In case of Hsp60 AA437-460 we found significantly decreased Th2 response in patients, although there was no significant difference in Th1 response. In case of Hsp60 AA394-408 and positive controls there was no significant difference.

Conclusion: Comparing the control and diabetic subjects a significant shift towards Th1 response in T1 diabetes mellitus for Hsp60 AA437-460 was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Case-Control Studies
  • Cells, Cultured
  • Chaperonin 60 / pharmacology*
  • Diabetes Mellitus, Type 1 / immunology*
  • Female
  • Health
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-13 / metabolism
  • Male
  • Middle Aged
  • Peptide Fragments / pharmacology*
  • Th1 Cells / drug effects*
  • Th1 Cells / immunology*
  • Th2 Cells / drug effects*
  • Th2 Cells / immunology*

Substances

  • Chaperonin 60
  • Interleukin-13
  • Peptide Fragments
  • Interferon-gamma