IMMUNOTHERAPY WITH FEL-D-1 PEPTIDES DECREASES IL-4 RELEASE BY PERIPHERAL-BLOOD T-CELLS OF PATIENTS ALLERGIC TO CATS

Background: Cells producing a T-H2-cytokine profile play an important role in the onset and maintenance of atopic diseases, and therefore sp ecific immunotherapy is aimed to induce a switch to cells producing a T-H1- or T-H0-cytokine profile. Recently, a novel form of immunotherap y making use of synthetic peptides from the major cat allergen Fel d 1 has been developed, but its mechanisms of action are unknown. Objecti ves: We examined the effects of immunotherapy with Fel dl peptides on the response to bronchial provocation tests (PD20FEV1) with a standard ized Fel d 1 cat extract on Fel d 1-specific serum IgE and IgG Levels and in vitro IL-4 and IFN-gamma production. Methods: Patients allergic to cats received 6 weekly injections of 7.5 mu g (Low dose), 75 mu g (medium dose), or 750 mu g (high dose) of Fel d 1 peptides (25 patient s) or a placebo (6 patients). Results: Six weeks after ending immunoth erapy, posttreatment PD20FEV1 was not significantly different between the treated and placebo groups. However, in the medium- and high-dose groups there was a significant improvement between baseline and posttr eatment days. IL-4 release was significantly reduced in the high dose- treated group (P < .005, Wilcoxon W test), whereas it was unchanged in the low or medium dose- and in the placebo-treated groups. In all gro ups, IFN-gamma, IgE, and IgG levels remained unchanged. Conclusion: Th ere was no correlation between the improvement of PD20FEV1 and the dec rease in IL-4 production, These data suggest that peptide immunotherap y may act by shifting, the Fel d 1-induced response of PBMCs in vitro from the T-H2-like to the T-H0-like phenotype.