Antiinflammatory properties of a peptide derived from interleukin-4

Research output: Contribution to journalArticle

Abstract

Interleukin-4 (IL-4) is a potent antiinflammatory cytokine. However its use in the clinic is hampered by side effects. We here describe the identification of a novel synthetic peptide, termed Ph8, derived from α-helix C of IL-4, which interacts with IL-4 receptor α (IL-4Rα). Employing various cultured genetically engineered cell lines and primary lymphocytes, surface plasmon resonance, qPCR, ELISA and immunoblotting techniques we found that Ph8 bound IL-4Rα and mimicked the anti-inflammatory effects of IL-4 by inhibiting TNF-α production by macrophages in vitro. It induced phosphorylation of STAT6 65. kD but inhibited phosphorylation of STAT6 110. kD induced by IL-4 in a B-cell line that expressed the type I receptor. It also inhibited the IL-4-stimulated expression of a STAT6-inducible reporter gene in cells that expressed the type II receptor. Ph8 inhibited the proliferation of Th1/2 cells and downregulated the production of IFN-γ in stimulated Th1 cells. Moreover, Ph8 did not induce any shift in Th1/Th2 profile. This is a favorable effect and it is indicating that Ph8 could block general T cell activation and inflammatory responses without further inducing the side effects generally associated with IL-4 signaling. These data collectively show that Ph8 is only a partial agonist of IL-4 mimicking its desirable properties. In agreement, Ph8 treatment of rats with collagen-induced arthritis, a Th1- and antibody- mediated disease of joint, delayed the manifestation of chronic inflammation and reduced acute inflammation in carrageenan-induced edema. Our findings indicate that Ph8 is a promising potential drug candidate for the treatment of inflammatory diseases.

Details

Authors
  • Boris Klementiev
  • Maj N. Enevoldsen
  • Shizhong Li
  • Robert Carlsson
  • Yawei Liu
  • Shohreh Issazadeh-Navikas
  • Elisabeth Bock
  • Vladimir Berezin
External organisations
  • University of Copenhagen
Research areas and keywords

Keywords

  • Collagen-induced arthritis, Interferon-γ, Interleukin-4, Signalling, Tumor necrosis factor-α
Original languageEnglish
Pages (from-to)112-121
Number of pages10
JournalCytokine
Volume64
Issue number1
Publication statusPublished - 2013 Oct 1
Publication categoryResearch
Peer-reviewedYes
Externally publishedYes