Evidence map›Paper›PMID 40270099›Full record

ArticleAllergy2025

Fish Allergenicity Ladder and Parvalbumin Epitopes for Predicting Clinical Cross-Reactivity and Reintroduction in Chinese Population.

Christine Y Y Wai, Nicki Y H Leung, Agnes S Y Leung, Man Fung Tang, Åsa Marknell DeWitt, Jaime S Rosa Duque, Gilbert T Chua, Yat Sun Yau, Wai Hung Chan, Po Ki Ho and 12 more

Abstract read
In one paragraph

Article in Allergy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

22 authors.

Christine Y Y WaiDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-2570-7745
Nicki Y H LeungDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-6836-6445
Agnes S Y LeungDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-8249-4478
Man Fung TangDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-3683-9217
Åsa Marknell DeWittThermo Fisher Scientific, ImmunoDiagnostics, Uppsala, Sweden.
Jaime S Rosa DuqueDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-5292-5510
Gilbert T ChuaDepartment of Paediatrics and Adolescent Medicine, The University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0003-0333-0059
Yat Sun YauDepartment of Paediatrics, Queen Elizabeth Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-5471-9139
Wai Hung ChanDepartment of Paediatrics, Queen Elizabeth Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-9256-4799
Po Ki HoDepartment of Paediatrics, Queen Elizabeth Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-7836-5243
Mike Y W KwanDepartment of Paediatrics and Adolescent Medicine, Princess Margaret Hospital and Yan Chai Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-1476-9625
Qun Ui LeeDepartment of Paediatrics and Adolescent Medicine, Princess Margaret Hospital and Yan Chai Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-6297-8969
Joshua S C WongDepartment of Paediatrics and Adolescent Medicine, Princess Margaret Hospital and Yan Chai Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0003-4815-5821
Ivan C S LamDepartment of Paediatrics and Adolescent Medicine, Princess Margaret Hospital and Yan Chai Hospital, Hong Kong SAR, China.
James W C H ChengDepartment of Paediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0003-1997-5230
David C K LukDepartment of Paediatrics and Adolescent Medicine, United Christian Hospital, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-7854-0221
Zhongyi LiuDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-5001-9186
Noelle Anne NgaiDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.
Oi Man ChanDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-8845-1428
Patrick S C LeungDivision of Rheumatology, Allergy and Clinical Immunology, University of California, Davis, California, USA.ORCID https://orcid.org/0000-0001-5862-4316
Gary W K WongDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0001-5939-812X
Ting Fan LeungDepartment of Paediatrics, The Chinese University of Hong Kong, Hong Kong SAR, China.ORCID https://orcid.org/0000-0002-6469-1926

Funding

Direct Grant for Research 2024.078Health and Medical Research Fund 08191356Health and Medical Research Fund 09202866Research Impact Fund of the Research Grants Council, Hong Kong SAR Government R4035-19
6 · The paper itself

Abstract

backgroundIgE-mediated fish allergy has long been considered an umbrella term due to the high cross-reactivity of parvalbumin, the major fish allergen. Yet, clinical tolerance to certain fish highlights allergenicity differences. In this study, we sought to construct a fish allergenicity ladder and identify fish parvalbumin epitopes to improve the diagnosis of fish allergy.

methodsReported clinical history and the serum-specific IgE (sIgE) responses of 200 Chinese subjects with suspected fish allergy were collected and analyzed, while the relative parvalbumin content in different fish was measured for the construction of a fish allergenicity ladder. Double-blind placebo-controlled food challenge (DBPCFC) and open challenge against salmon, grass carp, and grouper were performed in 58 selected patients for validation of the ladder. Epitope mapping was performed by peptide array against parvalbumins of salmon (both β-1 and β-2), cod, grouper, and grass carp with sera from fish allergic (n = 11), partial fish tolerant (n = 12), and complete fish tolerant (n = 5) patients diagnosed based on oral food challenge outcome.

resultsThe distribution pattern of reported history of fish allergy and tolerance, sIgE and molecular data, as well as their strong positive correlation led to the construction of a 3-step fish allergenicity ladder comprising: step 1 of the least allergenic fishes (tuna, halibut, salmon and cod), steps 2 of moderately allergenic fishes (herring and grouper) to step 3 of highly allergenic fishes (catfish, grass carp and tilapia). Epitope mapping revealed one epitope from grouper parvalbumin (AA64-78) for diagnosing general fish allergy and one epitopic region from salmon parvalbumin (AA19-33) as a biomarker of specific fish tolerance. Only epitope-specific IgE differentiated these patients but not sIgE to fish extract or parvalbumin.

conclusionThe fish ladder and epitopes discovery can precisely differentiate fish-allergic and tolerant subjects and guide fish reintroduction by stepping up the ladder, which innovates fish allergy care in the next millennium.

Indexed as

AllergensEpitopesFishesFood HypersensitivityParvalbuminsAdolescentAdultAnimalsChildChinaCross ReactionsEast Asian PeopleEpitope MappingFemaleFish ProteinsHumansAllergensEpitopesFish ProteinsImmunoglobulin EParvalbuminsclinical cross‐reactivityepitope mappingfood laddershome introductionIgE‐mediated fish allergy

Identifiers

PMID40270099
PMCPMC12486362

What OpenQuestion holds

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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.