Evidence map›Paper›PMID 31685862›Full record

ArticleScientific reports2019

Therapeutic potential of peptides from Ole e 1 in olive-pollen allergy.

David Calzada, Lucía Cremades-Jimeno, María Ángeles de Pedro, Selene Baos, Manuel Rial, Joaquín Sastre, Joaquín Quiralte, Fernando Florido, Carlos Lahoz, Blanca Cárdaba

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Sialic acid-modified der p 2 allergen exerts immunomodulatory effects on human PBMCs.The journal of allergy and clinical immunology. Global · 2024
    Article
  3. Review
  4. Review
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 6 institutions in 1 country.

David CalzadaImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
Lucía Cremades-JimenoImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
María Ángeles de PedroImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
Selene BaosImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
Manuel RialAllergy Department, Fundación Jiménez Díaz, Madrid, Spain.
Joaquín SastreAllergy Department, Fundación Jiménez Díaz, Madrid, Spain.
Joaquín QuiralteAllergy Department, Vírgen del Rocío University Hospital, Seville, Spain.
Fernando FloridoAllergy Department, San Cecilio University Hospital, Granada, Spain.
Carlos LahozImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain.
Blanca CárdabaImmunology Department, IIS-Fundación Jiménez Díaz, UAM, Madrid, Spain. bcardaba@fjd.es.
Centro de Investigación en Red en Enfermedades Cardiovasculares · ESHospital Universitario Fundación Jiménez Díaz · ESCentro de Investigación Biomédica en Red de Enfermedades Respiratorias · ESHospital Universitario Virgen del Rocío · ESInstituto de Investigación Biosanitaria de Granada · ESUniversidad Autónoma de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Olive-pollen allergy is one of the leading causes of respiratory allergy in Mediterranean countries and some areas of North America. Currently, allergen-specific immunotherapy is the only etiophatogenic treatment. However, this approach is not fully optimal, safe, or effective. Thus, efforts continue in the search for novel immunotherapy strategies, being one of the most promising the use of peptides derived from major allergens. This work tries to determine the therapeutic potential and safety of 5 dodecapeptides derived from the main allergen of olive-pollen allergy, Ole e 1. The immunomodulatory capacity of these peptides was studied using peripheral blood mononuclear cells (PBMCs) obtained from 19 olive-pollen-allergic patients and 10 healthy controls. We determined the capacity of these peptides to inhibit the proliferative response toward olive-pollen allergenic extract and to induce the regulatory cytokines, IL-10 and IL-35. To test the safety and absence of allergenicity of the peptides, the basophil activation was analyzed by flow-cytometry, using peripheral blood. The results showed that two of five peptides inhibited near to 30% the proliferative response against the total olive-pollen allergenic extract in olive-pollen-allergic patients. Inhibition increased to nearly 35% when the 5 peptides were used in combination. In both cases, a statistically significant induction of IL-10 and IL-35 secretion was observed in the supernatants of allergic patients PBMCs cultures. None of the 5 peptides induced basophil activation and cross-link inflammatory cell-bound IgE. In conclusion, these results open up new possibilities in the treatment of olive-pollen allergy, which could solve some of the problems facing current therapy approaches.

Indexed as

AdultAllergensAntibody SpecificityAntigens, PlantBasophilsCytokinesFemaleHumansImmunoglobulin EImmunophenotypingLeukocytes, MononuclearMaleMiddle AgedOleaPeptidesPlant ProteinsAllergensAntigens, PlantCytokinesImmunoglobulin EOle e I protein, Olea europaeaPeptidesPlant Proteins

Identifiers

PMID31685862
PMCPMC6828773
OpenAlexW2989121972

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.