Initial support for the hypothesis that PAR2 is involved in the immune response to Nippostrongylus brasiliensis in

Mark G Devlin1, Robin B Gasser, Tom M Cocks

  • 1Department of Pharmacology, The University of Melbourne, Parkville 3010, Melbourne, Victoria, Australia. markd@unimelb.edu.au

Parasitology Research
|April 27, 2007
PubMed

Insights

Protease-activated receptor 2 (PAR2) plays a role in parasitic helminth infections. Mice lacking PAR2 showed altered immune responses and parasite load, suggesting PAR2 recognizes nematode proteases.

Area of Science:

  • Immunology
  • Parasitology
  • Molecular Biology

Background:

  • Protease-activated receptor 2 (PAR2) is a cell surface receptor involved in inflammation and allergy.
  • The role of PAR2 in parasitic helminth infections remains unexplored.
  • PAR2 detects trypsin and trypsin-like enzymes.

Purpose of the Study:

  • To investigate the role of PAR2 in hosts infected with the parasitic nematode Nippostrongylus brasiliensis.
  • To determine if PAR2 recognizes nematode-derived proteases.

Main Methods:

  • Comparison of Nippostrongylus brasiliensis infectivity in PAR2-deficient (PAR2-/-) mice and wild-type controls (129SV).
  • Analysis of fecal egg counts and serum IgE levels.
  • In a separate study, BALB/c mice were co-administered ovalbumin with a PAR2-activating peptide (SLIGRL) or an inactive control peptide (LRGILS).
  • Assessment of IgE- and IL-10-expressing lymphocytes.

Main Results:

  • PAR2-/- mice exhibited increased fecal egg counts compared to controls.
  • PAR2-/- mice showed decreased total serum IgE levels.
  • Coadministration of ovalbumin and SLIGRL augmented IgE- and IL-10-expressing lymphocytes, unlike the inactive peptide.

Conclusions:

  • PAR2 appears to influence the host's immune response to Nippostrongylus brasiliensis infection.
  • Findings suggest PAR2 may function as a recognition receptor for proteases derived from nematodes.

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