A phosphorylcholine-containing filarial nematode-secreted product disrupts B lymphocyte activation by targeting key proliferative signaling pathways

J Immunol. 1998 Mar 15;160(6):2692-9.

Abstract

Filarial nematodes infect more than 100 million people in the tropics, causing elephantiasis, chronic skin lesions, and blindness. The parasites are long-lived as a consequence of being able to evade the host immune system, but an understanding of the molecular mechanisms underlying this evasion remains elusive. In this study, we demonstrate that ES-62 (2 microg/ml), a phosphorylcholine (PC)-containing glycoprotein released by the rodent filarial parasite Acanthocheilonema viteae, is able to polyclonally activate certain protein tyrosine kinase and mitogen-activating protein kinase signal-transduction elements in B lymphocytes. Although this interaction is insufficient to cause B lymphocyte proliferation per se, it serves to desensitize the cells to subsequent activation of the phosphoinositide-3-kinase and Ras mitogen-activating protein kinase pathways, and hence also to proliferation, via the Ag receptor. The active component of ES-62 appears to be PC, a molecule recently shown to act as an intracellular signal transducer, as the results obtained with ES-62 are broadly mimicked by PC alone. As PC-containing secreted products (PC-ES) are also released by human filarial parasites, our data suggest that PC-ES, by interfering with B cell function, could play a role in prolonging filarial infection in parasitized individuals.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / immunology
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Dipetalonema / physiology*
  • Helminth Proteins / pharmacology*
  • Humans
  • Lymphocyte Activation / drug effects*
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation
  • Phosphorylcholine / pharmacology*
  • Protein-Tyrosine Kinases / physiology
  • Rabbits
  • Sphingomyelin Phosphodiesterase / physiology
  • ras Proteins / metabolism

Substances

  • Helminth Proteins
  • Phosphorylcholine
  • Phosphatidylinositol 3-Kinases
  • Protein-Tyrosine Kinases
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Sphingomyelin Phosphodiesterase
  • ras Proteins