Immunologic mechanisms of a short-course of Lolium perenne peptide immunotherapy: A randomized, double-blind, placebo-controlled trial.

Sharif, Hanisah; Singh, Iesha; Kouser, Lubna; Mösges, Ralph; Bonny, Marie-Alix; Karamani, Angeliki; Parkin, Rebecca V; Bovy, Nicolas et al. · J Allergy Clin Immunol · 2019

rct · Level II

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Abstract

A 3-week short-course of adjuvant-free hydrolysates of Lolium perenne peptide (LPP) immunotherapy for rhinoconjunctivitis with or without asthma over 4 physician visits is safe, well tolerated, and effective. We sought to investigate immunologic mechanisms of LPP immunotherapy in a subset of patients who participated in a phase III, multicenter, randomized, double-blind, placebo-controlled trial (clinical.govNCT02560948). Participants were randomized to receive LPP (n = 21) or placebo (n = 11) for 3 weeks over 4 visits. Grass pollen-induced basophil, T-cell, and B-cell responses were evaluated before treatment (visit [V] 2), at the end of treatment (V6), and after the pollen season (V8). Combined symptom and rescue medication scores (CSMS) were lower during the peak pollen season (-35.1%, P = .03) and throughout the pollen season (-53.7%, P = .03) in the LPP-treated group compared with those in the placebo-treated group. Proportions of CD63<sup>+</sup> and CD203c<sup>bright</sup>CRTH2<sup>+</sup> basophils were decreased following LPP treatment at V6 (10 ng/mL, P < .0001) and V8 (10 ng/mL, P < .001) compared to V2. No change in the placebo-treated group was observed. Blunting of seasonal increases in levels of grass pollen-specific IgE was observed in LPP-treated but not placebo-treated group. LPP immunotherapy, but not placebo, was associated with a reduction in proportions of IL-4<sup>+</sup> T<sub>H</sub>2 (V6, P = .02), IL-4<sup>+</sup> (V6, P = .003; V8, P = .004), and IL-21<sup>+</sup> (V6, P = .003; V8, P = .002) follicular helper T cells. Induction of FoxP3<sup>+</sup>, follicular regulatory T, and IL-10<sup>+</sup> regulatory B cells were observed at V6 (all P < .05) and V8 (all P < .05) in LPP-treated group. Induction of regulatory B cells was associated with allergen-neutralizing IgG<sub>4</sub>-blocking antibodies. For the first time, we demonstrate that the immunologic mechanisms of LPP immunotherapy are underscored by immune modulation in the T- and B-cell compartments, which is necessary for its effect.

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