Evidence map›Paper›PMID 33784407›Full record

ArticleAllergy2021

Nanoarchitectures for efficient IgE cross-linking on effector cells to study amoxicillin allergy.

Amene Tesfaye, Alba Rodríguez-Nogales, Sara Benedé, Tahía D Fernández, Juan L Paris, Maria J Rodriguez, Isabel M Jiménez-Sánchez, Gador Bogas, Cristobalina Mayorga, María J Torres and 1 more

Abstract read
In one paragraph

Article in Allergy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

6 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. A Skin Testing Strategy for Non-IgE-Mediated Reactions Associated With Vancomycin.The journal of allergy and clinical immunology. In practice · 2024
    Article
  5. Article
  6. 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

11 authors.

Amene TesfayeAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.ORCID 0000-0003-0482-8895
Alba Rodríguez-NogalesAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.
Sara BenedéInstituto de Investigación en Ciencias de la Alimentación (CIAL, CSIC-UAM), Madrid, Spain.
Tahía D FernándezAllergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA, Málaga, Spain.ORCID 0000-0003-0625-2156
Juan L ParisAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.
Maria J RodriguezAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.
Isabel M Jiménez-SánchezAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.
Gador BogasAllergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA, Málaga, Spain.
Cristobalina MayorgaAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.ORCID 0000-0001-8852-8077
María J TorresAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.ORCID 0000-0001-5228-471X
María I MontañezAndalusian Centre for Nanomedicine and Biotechnology-BIONAND, Málaga, Spain.ORCID 0000-0001-6641-5979

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmoxicillin (AX) is nowadays the β-lactam that more frequently induces immediate allergic reactions. Nevertheless, diagnosis of AX allergy is occasionally challenging due to risky in vivo tests and non-optimal sensitivity of in vitro tests. AX requires protein haptenation to form multivalent conjugates with increased size to be immunogenic. Knowing adduct structural features for promoting effector cell activation would help to improve in vitro tests. We aimed to identify the optimal structural requirement in specific cellular degranulation to AX using well-precised nanoarchitectures of different lengths.

methodWe constructed eight Bidendron Antigens (BiAns) based on polyethylene glycol (PEG) linkers of different lengths (600-12,000 Da), end-coupled with polyamidoamine dendrons that were terminally multi-functionalized with amoxicilloyl (AXO). In vitro IgE recognition was studied by competitive radioallergosorbent test (RAST) and antibody-nanoarchitecture complexes by transmission electron microscopy (TEM). Their allergenic activity was evaluated using bone marrow-derived mast cells (MCs) passively sensitized with mouse monoclonal IgE against AX and humanized RBL-2H3 cells sensitized with polyclonal antibodies from sera of AX-allergic patients.

resultsAll BiAns were recognized by AX-sIgE. Dose-dependent activation responses were observed in both cellular assays, only with longer structures, containing spacers in the range of PEG 6000-12,000 Da. Consistently, greater proportion of immunocomplexes and number of antibodies per complex for longer BiAns were visualized by TEM.

conclusionsBiAns are valuable platforms to study the mechanism of effector cell activation. These nanomolecular tools have demonstrated the importance of the adduct size to promote effector cell activation in AX allergy, which will impact for improving in vitro diagnostics.

Indexed as

Drug HypersensitivityHypersensitivity, ImmediateAmoxicillinAnimalsHumansImmunoglobulin EMicePenicillinsAmoxicillinImmunoglobulin EPenicillinsamoxicillindrug allergyIgE cross-linkingimmunocomplexnanostructure

Identifiers

PMID33784407
PMCPMC8518075

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Registered trials

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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.