Evidence map›Paper›PMID 27979027›Full record

ArticleAnnals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology2016

Immunodominance in allergic T-cell reactivity to Japanese cedar in different geographic cohorts.

Carla Oseroff, John Pham, April Frazier, Denise Hinz, John Sidney, Sinu Paul, Jason A Greenbaum, Randi Vita, Bjoern Peters, Véronique Schulten and 1 more

Erratum issuedAbstract read
In one paragraph

Article in Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Carla OseroffLa Jolla Institute for Allergy and Immunology, La Jolla, California.
John PhamLa Jolla Institute for Allergy and Immunology, La Jolla, California.
April FrazierLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Denise HinzLa Jolla Institute for Allergy and Immunology, La Jolla, California.
John SidneyLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Sinu PaulLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Jason A GreenbaumLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Randi VitaLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Bjoern PetersLa Jolla Institute for Allergy and Immunology, La Jolla, California.
Véronique SchultenLa Jolla Institute for Allergy and Immunology, La Jolla, California. Electronic address: veronique@lji.org.
Alessandro SetteLa Jolla Institute for Allergy and Immunology, La Jolla, California.

Funding

Understanding mechanisms in specific immunotherapy (SIT)U19AI100275 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SETTE, ALESSANDRO · 2012 to 2017
$8.1M
HEPATITIS C VIRAL MUTANTS AND HUMAN T CELL FUNCTIONK01DK002970 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WANG, HUIRU · 2001 to 2003
$265k
NIAID NIH HHS U19 AI100275NIDDK NIH HHS K01 DK002970
6 · The paper itself

Abstract

backgroundJapanese cedar (JC) pollen is a common trigger for allergic rhinitis in Japan. Pollen proteins targeted by IgE, including Cry j 1 and Cry j 2, and isoflavone reductase (IFR) have been identified.

objectiveTo compare antigen-specific IgE titers and T-cell responses to JC pollen-derived extract and peptides in cohorts with high and low pollen exposure.

methodsPeripheral blood mononuclear cells from JC pollen allergic or nonallergic patients who have lived in Japan for at least 1 year and JC pollen allergic patients who have never been to Japan were tested for T-cell responses against JC pollen extract and peptide pools derived from Cry j 1, Cry j 2, or IFR. T-cell reactivity was assessed by interleukin 5 and interferon γ production by ELISPOT.

resultsJC pollen-specific T-cell reactivity and IgE titers were significantly higher in the allergic compared with the nonallergic Japanese cohort, which was also associated with different patterns of polysensitization. Interestingly, a significant overlap was observed in the hierarchy of the T-cell epitopes in the allergic Japanese cohort compared with the allergic non-Japanese cohort. In all 3 cohorts, T-cell reactivity was dominantly directed against peptides from the major allergens Cry j 1 and 2, with few T-cell responses detected against IFR.

conclusionOur studies identify common denominators of T-cell reactivity in patient populations with different sensitization patterns, suggesting that generally applicable immunotherapeutic approaches might be developed irrespective of exposure modality.

Indexed as

AdolescentAdultAllelesAllergensAmino Acid SequenceAntigens, PlantCohort StudiesCryptomeriaEpitopes, T-LymphocyteFemaleHLA AntigensHumansImmunoglobulin ELeukocytes, MononuclearLymphocyte ActivationMaleAllergensAntigens, PlantEpitopes, T-LymphocyteHLA AntigensImmunoglobulin EPeptides

Identifiers

PMID27979027
PMCPMC5172395

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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.