Evidence map›Paper›PMID 42676692›Full record

ArticleFrontiers in immunology2026

Bispecific nanobodies targeting Bet v 1 and ICAM-1 decrease respiratory epithelial penetration of Bet v 1.

Ines Zettl, Isabella Ellinger, Mohammed Zghaebi, Sarah Jance, Vanessa Izewski, Anja Drescher, Heimo Breiteneder, Manuel Röck, Martin Tollinger, Julia Eckl-Dorna and 2 more

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Ines ZettlInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Isabella EllingerInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Mohammed ZghaebiVienna Airway Lab, Department of Otolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.
Sarah JanceInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Vanessa IzewskiInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Anja DrescherCytiva Europe GmbH, Freiburg, Germany.
Heimo BreitenederInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Manuel RöckDepartment of Organic Chemistry, University of Innsbruck, Innsbruck, Austria.
Martin TollingerDepartment of Organic Chemistry, University of Innsbruck, Innsbruck, Austria.
Julia Eckl-DornaVienna Airway Lab, Department of Otolaryngology, Head and Neck Surgery, Medical University of Vienna, Vienna, Austria.
Sergei V TillibInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Sabine FlickerInstitute of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The major birch pollen allergen Bet v 1 primarily affects the nose and eyes of allergic patients. After crossing the epithelial barrier, it causes IgE-mediated effector cell release, triggering inflammatory responses. We sought to develop bispecific nanobodies that bind Bet v 1 on mucosal surfaces to prevent allergen penetration and subsequent activation of effector cells. Intercellular adhesion molecule 1 (ICAM-1), highly upregulated on epithelial cells of allergic individuals, was chosen as an anchor. Methods: Genetically fused nanobodies targeting Bet v 1 and ICAM-1 were generated and characterized for specificity, affinity, Bet v 1 immobilization on the surface of the human bronchial epithelial cell line, 16HBE14o-, and their potential to inhibit Bet v 1 penetration through a cell monolayer. Results: Bispecific nanobodies recognized ICAM-1, Bet v 1 and related tree pollen allergens (Aln g 1, Cor a 1). While we observed a clear co-localization of nanobodies and Bet v 1 on the 16HBE14o-cell surface after 30 min, Bet v 1 was slightly internalized after 4h at 32 °C. Dissociation rate constants between bispecific nanobodies and antigens were 3-6 times faster at 32 °C compared to 25 °C. Bispecific nanobodies reduced Bet v 1 penetration and hence decreased basophil activation. Conclusion: We generated bivalent nanobodies specific for ICAM-1 and Bet v 1. These nanobodies diminished trans-epithelial transport of Bet v 1 by ICAM-1-mediated immobilization at the cell surface. Reduced Bet v 1 penetration resulted in decreased basophil activation, demonstrating the potential of local administration of nanobodies for the prevention of pollen allergy.

Indexed as

AllergensAntibodies, BispecificAntigens, PlantIntercellular Adhesion Molecule-1Respiratory MucosaSingle-Domain AntibodiesCell LineEpithelial CellsHumansPollenAllergensAntibodies, BispecificAntigens, PlantBet v 1 allergen, BetulaICAM1 protein, humanIntercellular Adhesion Molecule-1Single-Domain Antibodiesbirch pollen allergybispecific nanobodyICAM-1respiratory epitheliumtopical treatment

Identifiers

PMID42676692
PMCPMC13527034

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.