Induction of interleukin-10 and suppressor of cytokine signalling-3 gene expression following peptide immunotherapy

Clin Exp Allergy. 2006 Apr;36(4):465-74. doi: 10.1111/j.1365-2222.2006.02469.x.

Abstract

Background: Allergen-derived (T cell epitope) peptides may be safer for immunotherapy than native allergen, as they do not cross-link immunoglobulin (Ig)E. However, HLA polymorphism results in multiple potential epitopes. Synthetic peptides of phospholipase (PL) A(2) were selected for a peptide vaccine, on the basis of binding affinity for commonly expressed HLA-DR molecules.

Objective: To evaluate treatment with an HLA-DR-based PLA(2) peptide vaccine in subjects with mild honeybee allergy in an open, controlled study.

Methods: Twelve volunteers with allergy to bee venom received nine intradermal injections of PLA(2) peptides, with six untreated subjects serving as controls. Outcome was assessed by the size of the late-phase cutaneous reaction to allergen, peripheral blood mononuclear cell (PBMC) proliferation, cytokine release, and expression of genes associated with immune regulation.

Results: Subjects receiving peptides showed a decrease in the magnitude of the late-phase cutaneous reaction to bee venom compared with controls (P=0.03). The proliferation of venom-stimulated PBMCs decreased in treated subjects compared with controls (P=0.01). Peptide treatment reduced the production of IL-13 by PLA(2)-stimulated PBMCs (P<0.01) and IFN-gamma (P<0.01), and increased the production of IL-10 (P=0.02). Transcription of the suppressor of cytokine signalling (Socs)3 gene was significantly increased following therapy. A transient, but modest, increase in allergen-specific IgG was also observed.

Conclusion: HLA-DR-based T cell epitopes modify surrogate markers associated with successful immunotherapy and induction of immune regulation, supporting the concept that this form of treatment may be efficacious in human allergic disease.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Bee Venoms / immunology*
  • Cell Division / immunology
  • Cytokines / immunology
  • Drug Hypersensitivity / genetics
  • Drug Hypersensitivity / immunology*
  • Drug Hypersensitivity / therapy
  • Epitopes, T-Lymphocyte / immunology
  • Female
  • Forkhead Transcription Factors / genetics
  • Gene Expression Regulation / immunology
  • HLA-DR Antigens / immunology
  • Humans
  • Immunoglobulin G / immunology
  • Immunohistochemistry / methods
  • Immunotherapy, Active / methods*
  • Injections, Intradermal
  • Interleukin-10 / immunology*
  • Interleukin-13 / immunology
  • Leukocytes, Mononuclear / immunology
  • Male
  • Peptides / immunology
  • Phospholipases A / administration & dosage*
  • Phospholipases A / immunology
  • Signal Transduction / genetics
  • Signal Transduction / immunology
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins / genetics*
  • Suppressor of Cytokine Signaling Proteins / immunology
  • Transcription Factors / immunology
  • Treatment Outcome

Substances

  • Bee Venoms
  • Cytokines
  • Epitopes, T-Lymphocyte
  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • HLA-DR Antigens
  • Immunoglobulin G
  • Interleukin-13
  • Peptides
  • SOCS3 protein, human
  • Suppressor of Cytokine Signaling 3 Protein
  • Suppressor of Cytokine Signaling Proteins
  • Transcription Factors
  • Interleukin-10
  • Phospholipases A