Monophosphoryl lipid A (MPL) promotes allergen-induced immune deviation in favour of Th1 responses

F Puggioni1, S R Durham, J N Francis

  • 1Division of Respiratory Medicine, IRCCS Policlinic San Matteo, University of Pavia, Pavia, Italy.

Allergy
|April 9, 2005
PubMed
Abstract

Insights

Monophosphoryl lipid A (MPL) shifts immune responses from Th2 to Th1 in grass pollen allergies. This adjuvant therapy, mediated by IL-12 and monocytes, shows potential for treating hay fever.

Area of Science:

  • Immunology
  • Allergy Research
  • Vaccine Adjuvants

Background:

  • Monophosphoryl lipid A (MPL) is a detoxified derivative of lipopolysaccharide (LPS).
  • MPL serves as an adjuvant in pollen vaccines for allergic rhinitis.
  • Its in vitro effects on cellular responses to allergens require further investigation.

Purpose of the Study:

  • To investigate the in vitro effects of MPL on peripheral blood mononuclear cells (PBMCs) from patients with grass pollen hay fever.
  • To determine MPL's influence on cellular proliferation and cytokine production in response to grass pollen allergens.

Main Methods:

  • PBMCs from 13 hay fever patients were cultured with grass pollen extract and MPL.
  • Cellular proliferation was assessed via thymidine incorporation.
  • Cytokine production (IFN-gamma, IL-5, IL-10) was measured using ELISA.
  • IL-12 neutralization and monocyte depletion were employed to elucidate mechanisms.

Main Results:

  • MPL did not affect cellular proliferation but significantly increased allergen-induced interferon-gamma (IFN-gamma) production.
  • MPL significantly decreased allergen-induced interleukin-5 (IL-5) production.
  • MPL-induced IFN-gamma elevation was inhibited by anti-IL-12 antibodies and abrogated by monocyte depletion.

Conclusions:

  • MPL promotes immune deviation from Th2 to Th1 responses against grass pollen allergens.
  • This immune modulation is dependent on interleukin-12 (IL-12) and monocytes.
  • MPL shows potential as an adjuvant for shifting allergic responses towards a Th1-mediated immunity.

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