Journal
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Volume 120, Issue 2, Pages 293-299Publisher
MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2007.03.017
Keywords
T-H(1)/T-H(2) cells; T-cell polarization; pollen allergy; phytoprostanes; pollen-associated lipid mediators
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Background: We recently demonstrated that pollen not only function as allergen carriers but also as rich sources of bioactive lipids, such as phytoprostanes, that modulate human dendritic cell (DC) function in a way that results in an enhanced T(H)2 polarization in vitro. Objective: Here we analyzed the immunomodulatory capacities of Betula alba (white birch) aqueous pollen extracts (Bet-APEs) and pollen-associated phytoprostanes in the murine system in vitro and in vivo. Methods: DC function was analyzed in vitro by using BALB/c bone marrow-derived DCs. T-cell responses were analyzed with DO11.10 peptide 323-339 from chicken ovalbumin (OVA)specific CD4 T cells as responder cells. For in vivo studies, OVA-specific CD4 T cells were adoptively transferred into BALB/c mice. Twenty-four hours later, mice were challenged by means of intranasal application of OVA in the absence or presence of Bet-APEs or phytoprostanes. Polarization of T-cell responses in vivo was analyzed in draining lymph node cells. Results: In vitro Bet-APEs and E-1-phytoprostanes dose-dependently inhibited LPS-induced IL-12p70 of DCs. In addition, Bet-APEs induced a TH2 polarization in vitro. Similarly, intranasal instillation of Bet-APEs in vivo, together with the antigen, lead to increased IL-4, IL-5, and IL-13 secretion and decreased IFN-gamma secretion from antigen-specific T cells in the draining lymph nodes. In contrast, intranasal E1- and F1-phytoprostanes downregulated both T(H)1 and T(H)2 cytokine production in vivo. Conclusion: Pollen release water-soluble factors that display T(H)2-polarizing capacities in vivo independently of E-1- and F-1-phytoprostanes. Clinical implications: Identification of the underlying mechanisms might open new approaches for pharmacologic intervention.
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