4.7 Article

Targeting immunodominant Bet v 1 epitopes with monoclonal antibodies prevents the birch allergic response

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 149, 期 1, 页码 200-211

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MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2021.05.038

关键词

Bet v 1; birch pollen allergy; mAbs; IgE; x-ray crystal-lography; cryo-electron microscopy

资金

  1. Regeneron Pharmaceuticals, Inc.

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This study demonstrates that a combination of mAbs targeting Bet v 1 can prevent the allergic response to birch pollen, highlighting the potential of allergen-specific antibody approaches in treating allergies.
Background: Blocking the major cat allergen, Fel d 1, with mAbs was effective in preventing an acute cat allergic response. Objectives: This study sought to extend the allergen-specific antibody approach and demonstrate that a combination of mAbs targeting Bet v 1, the immunodominant and most abundant allergenic protein in birch pollen, can prevent the birch allergic response. Methods: Bet v 1-specific mAbs, REGN5713, REGN5714, and REGN5715, were isolated using the VelocImmune platform. Surface plasmon resonance, x-ray crystallography, and cryoelectron microscopy determined binding kinetics and structural data. Inhibition of IgE-binding, basophil activation, and mast cell degranulation were assessed via blocking ELISA, flow cytometry, and the passive cutaneous anaphylaxis mouse model. Results: REGN5713, REGN5714, and REGN5715 bind with high affinity and noncompetitively to Bet v 1. A cocktail of all 3 antibodies, REGN5713/14/15, blocks IgE binding to Bet v 1 and inhibits Bet v 1- and birch pollen extract-induced basophil activation ex vivo and mast cell degranulation in vivo. Crystal structures of the complex of Bet v 1 with immunoglobulin antigen-binding fragments of REGN5713 or REGN5715 show distinct interaction sites on Bet v 1. Cryo-electron microscopy reveals a planar and roughly symmetrical complex formed by REGN5713/14/15 bound to Bet v 1. Conclusions: These data confirm the immunodominance of Bet v 1 in birch allergy and demonstrate blockade of the birch allergic response with REGN5713/14/15. Structural analyses show simultaneous binding of REGN5713, REGN5714, and REGN5715 with substantial areas of Bet v 1 exposed, suggesting that targeting specific epitopes is sufficient to block the allergic response. (J Allergy Clin Immunol 2022;149:200-11.)

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