Novel Noncompetitive IL-1 Receptor-Biased Ligand Prevents Infection- and Inflammation-Induced Preterm Birth

J Immunol. 2015 Oct 1;195(7):3402-15. doi: 10.4049/jimmunol.1500758. Epub 2015 Aug 24.

Abstract

Preterm birth (PTB) is firmly linked to inflammation regardless of the presence of infection. Proinflammatory cytokines, including IL-1β, are produced in gestational tissues and can locally upregulate uterine activation proteins. Premature activation of the uterus by inflammation may lead to PTB, and IL-1 has been identified as a key inducer of this condition. However, all currently available IL-1 inhibitors are large molecules that exhibit competitive antagonism properties by inhibiting all IL-1R signaling, including transcription factor NF-κB, which conveys important physiological roles. We hereby demonstrate the efficacy of a small noncompetitive (all-d peptide) IL-1R-biased ligand, termed rytvela (labeled 101.10) in delaying IL-1β-, TLR2-, and TLR4-induced PTB in mice. The 101.10 acts without significant inhibition of NF-κB, and instead selectively inhibits IL-1R downstream stress-associated protein kinases/transcription factor c-jun and Rho GTPase/Rho-associated coiled-coil-containing protein kinase signaling pathways. The 101.10 is effective at decreasing proinflammatory and/or prolabor genes in myometrium tissue and circulating leukocytes in all PTB models independently of NF-κB, undermining NF-κB role in preterm labor. In this work, biased signaling modulation of IL-1R by 101.10 uncovers a novel strategy to prevent PTB without inhibiting NF-κB.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Female
  • Inflammation / immunology*
  • Interleukin-1beta / immunology
  • JNK Mitogen-Activated Protein Kinases / antagonists & inhibitors*
  • Mice
  • Myometrium / metabolism
  • NF-kappa B / metabolism
  • Peptides / pharmacology*
  • Pregnancy
  • Premature Birth / prevention & control*
  • Receptors, Interleukin-1 / antagonists & inhibitors
  • Toll-Like Receptor 2 / immunology
  • Toll-Like Receptor 4 / immunology
  • Uterus / immunology
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors*
  • rho GTP-Binding Proteins / antagonists & inhibitors
  • rho-Associated Kinases / antagonists & inhibitors

Substances

  • 101.10 peptide
  • IL1B protein, mouse
  • Interleukin-1beta
  • NF-kappa B
  • Peptides
  • Receptors, Interleukin-1
  • Tlr2 protein, mouse
  • Tlr4 protein, mouse
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • rho-Associated Kinases
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • rho GTP-Binding Proteins