Evidence map›Paper›PMID 27359111›Full record

ArticleClinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology2016

Sequence conservation predicts T cell reactivity against ragweed allergens.

J Pham, C Oseroff, D Hinz, J Sidney, S Paul, J Greenbaum, R Vita, E Phillips, S Mallal, B Peters and 1 more

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
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  9. Article
  10. Immunodominance in allergic T-cell reactivity to Japanese cedar in different geographic cohorts.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2016
    Article
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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

11 authors at 2 institutions in 2 countries.

J PhamLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
C OseroffLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
D HinzLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
J SidneyLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
S PaulLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
J GreenbaumLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
R VitaLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
E PhillipsInstitute for Immunology and Infectious Diseases, Murdoch University, Perth, WA, Australia.
S MallalInstitute for Immunology and Infectious Diseases, Murdoch University, Perth, WA, Australia.
B PetersLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
A SetteLa Jolla Institute for Allergy and Immunology, La Jolla, CA, USA.
La Jolla Institute for Immunology · USVanderbilt University · US

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

backgroundRagweed is a major cause of seasonal allergy, affecting millions of people worldwide. Several allergens have been defined based on IgE reactivity, but their relative immunogenicity in terms of T cell responses has not been studied.

objectiveWe comprehensively characterized T cell responses from atopic, ragweed-allergic subjects to Amb a 1, Amb a 3, Amb a 4, Amb a 5, Amb a 6, Amb a 8, Amb a 9, Amb a 10, Amb a 11, and Amb p 5 and examined their correlation with serological reactivity and sequence conservation in other allergens.

methodsPeripheral blood mononuclear cells (PBMCs) from donors positive for IgE towards ragweed extracts after in vitro expansion for secretion of IL-5 (a representative Th2 cytokine) and IFN-γ (Th1) in response to a panel of overlapping peptides spanning the above-listed allergens were assessed.

resultsThree previously identified dominant T cell epitopes (Amb a 1 176-191, 200-215, and 344-359) were confirmed, and three novel dominant epitopes (Amb a 1 280-295, 304-319, and 320-335) were identified. Amb a 1, the dominant IgE allergen, was also the dominant T cell allergen, but dominance patterns for T cell and IgE responses for the other ragweed allergens did not correlate. Dominance for T cell responses correlated with conservation of ragweed epitopes with sequences of other well-known allergens. CONCLUSIONS AND CLINICAL RELEVANCE: These results provide the first assessment of the hierarchy of T cell reactivity in ragweed allergens, which is distinct from that observed for IgE reactivity and influenced by T cell epitope sequence conservation. The results suggest that ragweed allergens associated with lesser IgE reactivity and significant T cell reactivity may be targeted for T cell immunotherapy, and further support the development of immunotherapies against epitopes conserved across species to generate broad reactivity against many common allergens.

Indexed as

Conserved SequenceAdolescentAdultAllergensAmbrosiaAmino Acid SequenceAntigens, PlantEpitopes, T-LymphocyteFemaleGene Expression ProfilingHistocompatibility TestingHumansImmunodominant EpitopesImmunoglobulin ELeukocytes, MononuclearMaleAllergensAmb a I protein, Ambrosia artemisiifoliaAntigens, PlantEpitopes, T-LymphocyteImmunodominant EpitopesImmunoglobulin EPeptidesPlant ProteinsallergensragweedT cell epitopes

Identifiers

PMID27359111
PMCPMC5007187
OpenAlexW2469749490

What OpenQuestion holds

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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 OpenQuestion graph.