Evidence map›Paper›PMID 42313883›Full record

ArticleClinical and translational allergy2026

Allergen Immunotherapy for the Treatment of Eosinophilic Esophagitis. An EAACI Task Force Systematic Review.

Martina Votto, Georgios Rentzos, Darío Antolin-Amerigo, Barbara Rymarczyk, George N Konstantinou, Adam T Fox, Antonella Cianferoni, Arzu Bakirtas, Carlo Maria Rossi, Marina Tsoumani and 8 more

Abstract read
In one paragraph

Article in Clinical and translational allergy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Martina VottoMaternity and Pediatric Department, Azienda Sanitaria Locale, Benevento, Italy.ORCID https://orcid.org/0000-0002-4271-8649
Georgios RentzosDepartment of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0002-2892-1923
Darío Antolin-AmerigoAllergy Department, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Universidad de Alcalá, Madrid, Spain.ORCID https://orcid.org/0000-0001-5699-4022
Barbara RymarczykDepartment of Internal Diseases, Allergology and Clinical Immunology, Medical University of Silesia, Katowice, Poland.ORCID https://orcid.org/0000-0002-9653-0801
George N KonstantinouDepartment of Allergy and Clinical Immunology, 424 General Military Training Hospital, Thessaloniki, Greece.ORCID https://orcid.org/0000-0003-1371-6764
Adam T FoxDepartment of Paediatric Allergy, Evelina London Children's Hospital, London, UK.ORCID https://orcid.org/0000-0002-3533-9798
Antonella CianferoniThe Children's Hospital of Philadelphia, University of Pennsylvania Medical School, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-2966-2564
Arzu BakirtasDepartment of Pediatric Allergy and Immunology, Faculty of Medicine, Gazi University, Ankara, Türkiye.ORCID https://orcid.org/0000-0002-7694-8944
Carlo Maria RossiFirst Department of Internal Medicine, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.ORCID https://orcid.org/0000-0003-1314-361X
Marina TsoumaniAllergy Centre, Wythenshawe Hospital, Manchester University Hospitals NHS Foundation Trust, Manchester, UK.ORCID https://orcid.org/0000-0002-9483-4705
Enrico HefflerDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Italy.ORCID https://orcid.org/0000-0002-0492-5663
Ingrid TerreehorstDepartment of Otorhinolaryngology and Head & Neck Surgery, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands.ORCID https://orcid.org/0000-0002-3264-2740
Evangelia C ApostolidouAllergy and Clinical Immunology, Private Practice, Thessaloniki, Greece.ORCID https://orcid.org/0000-0002-0277-606X
Maria Beatrice BilóDepartment of Clinical and Molecular Sciences, Polytechnic University of Marche, Ancona, Italy.ORCID https://orcid.org/0000-0002-9324-6039
Oliver PfaarDepartment of Otorhinolaryngology, Head and Neck Surgery, Section of Rhinology and Allergy, University Hospital Marburg, Philipps-Universität, Marburg, Germany.ORCID https://orcid.org/0000-0003-4374-9639
Alfredo J LucendoDepartment of Gastroenterology, Hospital General de Tomelloso, Tomelloso, Spain.ORCID https://orcid.org/0000-0003-1183-1072
Georgios K NikolopoulosMedical School, University of Cyprus, Nicosia, Cyprus.ORCID https://orcid.org/0000-0002-3307-0246
Constantinos PitsiosMedical School, University of Cyprus, Nicosia, Cyprus.ORCID https://orcid.org/0000-0001-8935-278X

Funding

The European Academy of Allergy and Clinical Immunology
6 · The paper itself

Abstract

backgroundMultiple routes of allergen immunotherapy (AIT) are approved for several IgE-mediated allergic diseases; however, the use of AIT in eosinophilic esophagitis (EoE) remains controversial and is supported by limited evidence. This review, conducted within the frame of an EAACI Task Force, aims to systematically evaluate the use of AIT as a potential treatment for EoE.

methodsThe protocol was registered and prepared in accordance with PRISMA guidelines. The literature search was conducted across three online databases (PubMed, Embase, and Scopus) and included studies published through January 31

resultsFour articles met the inclusion criteria. Three articles evaluated EPIT for milk-induced EoE in pediatric patients, all from the SMILEE (Study of Efficacy and Safety of Viaskin Milk for milk-induced EoE) trial and its extensions. These included a randomized, placebo-controlled trial, its open-label extension, and a pilot immunological study. The SMILEE trial found no statistically significant difference in tissue eosinophilia between the active (EPIT) and control (placebo) arms in the intention-to-treat population, while 47% of treated EoE patients tolerated milk without recurrence of esophageal eosinophilia. This finding was further supported by a subsequent open-label study with a 2-year follow-up. In the third publication, the researchers found that EPIT was associated with decreased Th2-related transcripts and increased regulatory T-cell-associated transcripts. Only one eligible study evaluated the use of SCIT for treating EoE. It was a retrospective case-control study reporting that SCIT had a neutral effect and yielded inconclusive findings regarding the course of EoE.

conclusionThere is insufficient high-quality evidence to support the effectiveness of alternative routes of AIT for the treatment of EoE, either as an add-on or a standalone treatment.

Indexed as

allergen immunotherapyeosinophilic esophagitisepicutaneous immunotherapysubcutaneous immunotherapy

Identifiers

PMID42313883
PMCPMC13278027

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.