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Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment

The nasal cavity is an important site of allergen entry. Hence, it represents an organ where trans-epithelial allergen penetration and subsequent IgE-mediated allergic inflammation can potentially be inhibited. Intercellular adhesion molecule 1 (ICAM-1) is highly expressed on the surface of respirat...

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Autores principales: Zettl, Ines, Ivanova, Tatiana, Zghaebi, Mohammed, Rutovskaya, Marina V., Ellinger, Isabella, Goryainova, Oksana, Kollárová, Jessica, Villazala-Merino, Sergio, Lupinek, Christian, Weichwald, Christina, Drescher, Anja, Eckl-Dorna, Julia, Tillib, Sergei V., Flicker, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682242/
https://www.ncbi.nlm.nih.gov/pubmed/36439110
http://dx.doi.org/10.3389/fimmu.2022.1022418
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author Zettl, Ines
Ivanova, Tatiana
Zghaebi, Mohammed
Rutovskaya, Marina V.
Ellinger, Isabella
Goryainova, Oksana
Kollárová, Jessica
Villazala-Merino, Sergio
Lupinek, Christian
Weichwald, Christina
Drescher, Anja
Eckl-Dorna, Julia
Tillib, Sergei V.
Flicker, Sabine
author_facet Zettl, Ines
Ivanova, Tatiana
Zghaebi, Mohammed
Rutovskaya, Marina V.
Ellinger, Isabella
Goryainova, Oksana
Kollárová, Jessica
Villazala-Merino, Sergio
Lupinek, Christian
Weichwald, Christina
Drescher, Anja
Eckl-Dorna, Julia
Tillib, Sergei V.
Flicker, Sabine
author_sort Zettl, Ines
collection PubMed
description The nasal cavity is an important site of allergen entry. Hence, it represents an organ where trans-epithelial allergen penetration and subsequent IgE-mediated allergic inflammation can potentially be inhibited. Intercellular adhesion molecule 1 (ICAM-1) is highly expressed on the surface of respiratory epithelial cells in allergic patients. It was identified as a promising target to immobilize antibody conjugates bispecific for ICAM-1 and allergens and thereby block allergen entry. We have previously characterized a nanobody specific for the major birch pollen allergen Bet v 1 and here we report the generation and characterization of ICAM-1-specific nanobodies. Nanobodies were obtained from a camel immunized with ICAM-1 and a high affinity binder was selected after phage display (Nb44). Nb44 was expressed as recombinant protein containing HA- and His-tags in Escherichia coli (E.coli) and purified via affinity chromatography. SDS-PAGE and Western blot revealed a single band at approximately 20 kDa. Nb44 bound to recombinant ICAM-1 in ELISA, and to ICAM-1 expressed on the human bronchial epithelial cell line 16HBE14o- as determined by flow cytometry. Experiments conducted at 4°C and at 37°C, to mimic physiological conditions, yielded similar percentages (97.2 ± 1.2% and 96.7 ± 1.5% out of total live cells). To confirm and visualize binding, we performed immunofluorescence microscopy. While Texas Red Dextran was rapidly internalized Nb44 remained localized on the cell surface. Additionally, we determined the strength of Nb44 and ICAM-1 interaction using surface plasmon resonance (SPR). Nb44 bound ICAM-1 with high affinity (10(-10) M) and had slow off-rates (10(-4) s(-1)). In conclusion, our results showed that the selected ICAM-1-specific nanobody bound ICAM-1 with high affinity and was not internalized. Thus, it could be further used to engineer heterodimers with allergen-specific nanobodies in order to develop topical treatments of pollen allergy.
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spelling pubmed-96822422022-11-24 Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment Zettl, Ines Ivanova, Tatiana Zghaebi, Mohammed Rutovskaya, Marina V. Ellinger, Isabella Goryainova, Oksana Kollárová, Jessica Villazala-Merino, Sergio Lupinek, Christian Weichwald, Christina Drescher, Anja Eckl-Dorna, Julia Tillib, Sergei V. Flicker, Sabine Front Immunol Immunology The nasal cavity is an important site of allergen entry. Hence, it represents an organ where trans-epithelial allergen penetration and subsequent IgE-mediated allergic inflammation can potentially be inhibited. Intercellular adhesion molecule 1 (ICAM-1) is highly expressed on the surface of respiratory epithelial cells in allergic patients. It was identified as a promising target to immobilize antibody conjugates bispecific for ICAM-1 and allergens and thereby block allergen entry. We have previously characterized a nanobody specific for the major birch pollen allergen Bet v 1 and here we report the generation and characterization of ICAM-1-specific nanobodies. Nanobodies were obtained from a camel immunized with ICAM-1 and a high affinity binder was selected after phage display (Nb44). Nb44 was expressed as recombinant protein containing HA- and His-tags in Escherichia coli (E.coli) and purified via affinity chromatography. SDS-PAGE and Western blot revealed a single band at approximately 20 kDa. Nb44 bound to recombinant ICAM-1 in ELISA, and to ICAM-1 expressed on the human bronchial epithelial cell line 16HBE14o- as determined by flow cytometry. Experiments conducted at 4°C and at 37°C, to mimic physiological conditions, yielded similar percentages (97.2 ± 1.2% and 96.7 ± 1.5% out of total live cells). To confirm and visualize binding, we performed immunofluorescence microscopy. While Texas Red Dextran was rapidly internalized Nb44 remained localized on the cell surface. Additionally, we determined the strength of Nb44 and ICAM-1 interaction using surface plasmon resonance (SPR). Nb44 bound ICAM-1 with high affinity (10(-10) M) and had slow off-rates (10(-4) s(-1)). In conclusion, our results showed that the selected ICAM-1-specific nanobody bound ICAM-1 with high affinity and was not internalized. Thus, it could be further used to engineer heterodimers with allergen-specific nanobodies in order to develop topical treatments of pollen allergy. Frontiers Media S.A. 2022-11-09 /pmc/articles/PMC9682242/ /pubmed/36439110 http://dx.doi.org/10.3389/fimmu.2022.1022418 Text en Copyright © 2022 Zettl, Ivanova, Zghaebi, Rutovskaya, Ellinger, Goryainova, Kollárová, Villazala-Merino, Lupinek, Weichwald, Drescher, Eckl-Dorna, Tillib and Flicker https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Zettl, Ines
Ivanova, Tatiana
Zghaebi, Mohammed
Rutovskaya, Marina V.
Ellinger, Isabella
Goryainova, Oksana
Kollárová, Jessica
Villazala-Merino, Sergio
Lupinek, Christian
Weichwald, Christina
Drescher, Anja
Eckl-Dorna, Julia
Tillib, Sergei V.
Flicker, Sabine
Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title_full Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title_fullStr Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title_full_unstemmed Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title_short Generation of high affinity ICAM-1-specific nanobodies and evaluation of their suitability for allergy treatment
title_sort generation of high affinity icam-1-specific nanobodies and evaluation of their suitability for allergy treatment
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682242/
https://www.ncbi.nlm.nih.gov/pubmed/36439110
http://dx.doi.org/10.3389/fimmu.2022.1022418
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