Stallergenes Greer, Antony, France.
Anergis SA, Epalinges, Switzerland.
Clin Exp Allergy. 2021 Feb;51(2):339-349. doi: 10.1111/cea.13814. Epub 2021 Jan 6.
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.
To identify a safe presentation platform able to enhance allergen-specific tolerance induction.
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.
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.
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.
舌下过敏原免疫疗法(AIT)通常在没有任何佐剂或给药系统的情况下进行,但有强有力的科学依据表明,通过使用适当的递呈平台,更好地将过敏原靶向到已知支持调节性免疫应答的口腔树突状细胞,可以提高治疗效果。
确定一种安全的递呈平台,能够增强过敏原特异性耐受诱导。
评估含有膜整合连续重叠肽(COPs)的水疱性口炎病毒(VSV)和 TLR4 或 TLR2/TLR7 激动剂的 Virosomes 能否诱导 Bet v 1 特异性 IgG1、IgG2a 和 IgE 抗体产生、过敏反应和体温下降,方法是将其皮下注射到 naive CD-1 小鼠中。最有前途的候选物是将 Bet v 1 COPs 锚定在含有膜内 TLR4 激动剂的 Virosomes 上(Vir.A-Bet v 1 COPs),然后在 BALB/c 小鼠中进行过敏性哮喘的舌下治疗评估。进一步评估气道高反应性、支气管肺泡灌洗液中的促炎细胞和肺部和脾脏中的 Th 细胞极化。
两种类型的佐剂化 VSV 与 Bet v 1 COPs 偶联都引发了增强的 Th1 免疫。鉴于更有利的安全性特征,进一步评估了 Vir.A-Bet v 1 COPs,并证明它能够在桦树花粉过敏的舌下治疗模型中完全逆转哮喘症状和肺部炎症。
我们首次报道了一种新型安全的递呈平台,即含有膜整合 TLR4 激动剂的水疱性口炎病毒(VSV),由于其内在的靶向和刺激双重特性,能够显著提高舌下 AIT 疗效,进一步促进抗过敏免疫反应。因此,我们的研究为进一步开发这种过敏原递呈平台用于治疗呼吸道过敏患者铺平了道路。