期刊
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 144, 期 3, 页码 738-749出版社
MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2019.02.023
关键词
Allergy; peptide immunotherapy; follicular helper T cells; regulatory T cells; regulatory B cells
资金
- ASIT Biotech S.A., Brussels, Belgium
Background: 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. Objective: 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 (clinicaLgovNCT02560948). Methods: 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). Results: 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(+) and CD203c(bright)CRTH2(+) basophils were decreased following LPP treatment at V6 (10 ngl 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(+) T(H)2 (V6, P =.02), IL-4(+) (V6, P =.003; V8, P =.004), and IL-21(+) (V6, P =.003; V8, P =.002) follicular helper T cells. Induction of FoxP3(+), follicular regulatory T, and IL-10+ 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 IgG4-blocking antibodies. Conclusion: 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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