Bet v 1 contiguous overlapping peptides anchored to virosomes with TLR4 agonist enhance immunotherapy efficacy in mice

被引:3
|
作者
Airouche, Sabi [1 ]
Beltrami, Vanya [2 ]
Fleury, Sylvain [3 ]
Batard, Thierry [1 ]
Bordas-Le Floch, Veronique [1 ]
Stegmann, Toon [4 ]
Amacker, Mario [3 ,5 ]
Kettner, Alexander [2 ]
Mascarell, Laurent [1 ]
机构
[1] Stallergenes Greer, Antony, France
[2] Anergis SA, Epalinges, Switzerland
[3] Mymet SA, Epalinges, Switzerland
[4] Mymet BV, Leiden, Netherlands
[5] Univ Bern, Bern Univ Hosp, Dept Pulm Med, Bern, Switzerland
来源
CLINICAL AND EXPERIMENTAL ALLERGY | 2021年 / 51卷 / 02期
关键词
allergen immunotherapy; Bet v 1 contiguous overlapping peptides; virosomes;
D O I
10.1111/cea.13814
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Whereas sublingual allergen immunotherapy (AIT) is routinely performed without any adjuvant or delivery system, there is a strong scientific rationale to better target the allergen(s) to oral dendritic cells known to support regulatory immune responses by using appropriate presentation platforms. Objective To identify a safe presentation platform able to enhance allergen-specific tolerance induction. Methods Virosomes with membrane-integrated contiguous overlapping peptides (COPs) of Bet v 1 and TLR4 or TLR2/TLR7 agonists were assessed for induction of Bet v 1-specific IgG1, IgG2a and IgE antibodies, hypersensitivity reactions and body temperature drop following subcutaneous injection in naive CD-1 mice. The most promising candidate, Bet v 1 COPs anchored to virosomes with membrane-incorporated TLR4 agonist (Vir.A-Bet v 1 COPs), was further evaluated by the sublingual route in a therapeutic setting in BALB/c mice with birch pollen-induced allergic asthma. Airway hyperresponsiveness, pro-inflammatory cells in bronchoalveolar lavages and polarization of Th cells in the lungs and spleen were then assessed. Results Both types of adjuvanted virosomes coupled to Bet v 1 COPs triggered a boosted Th1 immunity. Given a more favourable safety profile, Vir.A-Bet v 1 COPs were further evaluated and shown to able to fully reverse asthma symptoms and lung inflammation in a sublingual therapeutic model of birch pollen allergy. Conclusions and Clinical Relevance We report herein for the first time on the capacity of a novel and safe presentation platform, that is virosomes with membrane-integrated TLR4 agonist, to improve dramatically sublingual AIT efficacy in a murine model due to its intrinsic dual properties of targeting and stimulating to further promote anti-allergic immune responses. As such, our study paves the ground for further clinical development of this allergen presentation platform for patients suffering from respiratory allergies.
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页码:339 / 349
页数:11
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