Evidence map›Paper›PMID 36439110›Full record

ArticleFrontiers in immunology2022

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

Ines Zettl, Tatiana Ivanova, Mohammed Zghaebi, Marina V Rutovskaya, Isabella Ellinger, Oksana Goryainova, Jessica Kollárová, Sergio Villazala-Merino, Christian Lupinek, Christina Weichwald and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Single-Domain Antibodies-Novel Tools to Study and Treat Allergies.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 2 countries.

Ines ZettlDivision of Immunopathology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Tatiana IvanovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Mohammed ZghaebiDepartment of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.
Marina V RutovskayaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Isabella EllingerDivision of Cellular and Molecular Pathophysiology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Oksana GoryainovaInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Jessica KollárováDivision of Immunopathology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Sergio Villazala-MerinoDepartment of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.
Christian LupinekDivision of Immunopathology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Christina WeichwaldDivision of Immunopathology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Anja DrescherCytiva Europe GmbH, Freiburg, Germany.
Julia Eckl-DornaDepartment of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.
Sergei V TillibInstitute of Gene Biology, Russian Academy of Sciences, Moscow, Russia.
Sabine FlickerDivision of Immunopathology, Institute for Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
Medical University of Vienna · ATInstitute of Gene Biology · RUSevertsov Institute of Ecology and Evolution · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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

Indexed as

HypersensitivityRhinitis, Allergic, SeasonalSingle-Domain AntibodiesAllergensAnimalsCamelusHumansIntercellular Adhesion Molecule-1AllergensIntercellular Adhesion Molecule-1Single-Domain Antibodiesallergyhigh affinityICAM-1nanobodyVHH

Identifiers

PMID36439110
PMCPMC9682242
OpenAlexW4308652232

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.