Evidence map›Paper›PMID 27731424›Full record

ArticleScientific reports2016

The influence of the carrier molecule on amoxicillin recognition by specific IgE in patients with immediate hypersensitivity reactions to betalactams.

Adriana Ariza, Cristobalina Mayorga, María Salas, Inmaculada Doña, Ángela Martín-Serrano, Ezequiel Pérez-Inestrosa, Dolores Pérez-Sala, Antonio E Guzmán, María I Montañez, María J Torres

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 29 citations in OpenAlex.

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  15. The Value of In Vitro Tests to DiminishDrug Challenges.International journal of molecular sciences · 2017
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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

10 authors at 4 institutions in 1 country.

Adriana ArizaResearch Laboratory, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
Cristobalina MayorgaResearch Laboratory, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
María SalasAllergy Unit, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
Inmaculada DoñaAllergy Unit, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
Ángela Martín-SerranoResearch Laboratory, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
Ezequiel Pérez-InestrosaAndalusian Center for Nanomedicine and Biotechnology - BIONAND, Málaga, Spain.
Dolores Pérez-SalaCentro de Investigaciones Biológicas, CSIC, Madrid, Spain.
Antonio E GuzmánPharmacy Unit, Regional University Hospital of Malaga, Málaga, Spain.
María I MontañezResearch Laboratory, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
María J TorresAllergy Unit, IBIMA-Regional University Hospital of Malaga-UMA, Málaga, Spain.
Hospital Regional Universitario de Málaga · ESAndalusian Centre for Nanomedicine and Biotechnology · ESInstituto de Investigación Biomédica de Málaga · ESCentro de Investigaciones Biológicas Margarita Salas · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The optimal recognition of penicillin determinants, including amoxicillin (AX), by specific IgE antibodies is widely believed to require covalent binding to a carrier molecule. The nature of the carrier and its contribution to the antigenic determinant is not well known. Here we aimed to evaluate the specific-IgE recognition of different AX-derived structures. We studied patients with immediate hypersensitivity reactions to AX, classified as selective or cross-reactors to penicillins. Competitive immunoassays were performed using AX itself, amoxicilloic acid, AX bound to butylamine (AXO-BA) or to human serum albumin (AXO-HSA) in the fluid phase, as inhibitors, and amoxicilloyl-poli-L-lysine (AXO-PLL) in the solid-phase. Two distinct patterns of AX recognition by IgE were found: Group A showed a higher recognition of AX itself and AX-modified components of low molecular weights, whilst Group B showed similar recognition of both unconjugated and conjugated AX. Amoxicilloic acid was poorly recognized in both groups, which reinforces the need for AX conjugation to a carrier for optimal recognition. Remarkably, IgE recognition in Group A (selective responders to AX) is influenced by the mode of binding and/or the nature of the carrier; whereas IgE in Group B (cross-responders to penicillins) recognizes AX independently of the nature of the carrier.

Indexed as

AdultAgedAmoxicillinAnaphylaxisAntibody Specificitybeta-LactamsButylaminesCarrier ProteinsCross ReactionsDrug HypersensitivityFemaleHaptensHumansHypersensitivity, ImmediateImmunoglobulin EMaleAmoxicillinamoxicilloic acidbeta-LactamsButylaminesCarrier ProteinsHaptensImmunoglobulin EPenicillinsPolylysineSerum Albumin, Human

Identifiers

PMID27731424
PMCPMC5059705
OpenAlexW2530506616

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.