Evidence map›Paper›PMID 25505954›Full record

ArticleClinical & translational immunology2014

Invariant natural killer T-cell neutralization is a possible novel therapy for human eosinophilic esophagitis.

Madhavi Rayapudi, Priya Rajavelu, Xiang Zhu, Ajay Kaul, Rituraj Niranjan, Scott Dynda, Akanksha Mishra, Jochen Mattner, Asifa Zaidi, Parmesh Dutt and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Minimally invasive biomarker studies in eosinophilic esophagitis: A systematic review.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2018
    Pooled it
  2. Article
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  4. Review
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  11. Review
  12. Significance of Interleukin (IL)-15 in IgE associated eosinophilic Esophagitis (EoE).International journal of basic and clinical immunology · 2019
    Article
  13. Review
  14. Review
  15. IL-15 regulates fibrosis and inflammation in a mouse model of chronic pancreatitis.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  16. Pathophysiology of Eosinophilic Esophagitis.Clinical reviews in allergy & immunology · 2018
    Review
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 4 institutions in 2 countries.

Madhavi RayapudiDepartment of Pathology, University of Cincinnati , Cincinnati, OH, USA.
Priya RajaveluDivision of Pulmonary Biology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH , USA.
Xiang ZhuDivision of Allergy and Immunology, Cincinnati Children's Hospital Medical Center , Cincinnati, OH, USA.
Ajay KaulDivision of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center , Cincinnati, OH, USA.
Rituraj NiranjanDivision of Gastroenterology and Liver Disease, Case Western Reserve University , Cleveland, OH, USA.
Scott DyndaDivision of Gastroenterology and Liver Disease, Case Western Reserve University , Cleveland, OH, USA.
Akanksha MishraBiomedical Engineering, Case Western Reserve University , Cleveland, OH, USA.
Jochen MattnerDivision of Immunobiology, Cincinnati Children's Hospital Medical Center ; Cincinnati, OH, USA ; Mikrobiologisches Institut-Klinische Mikrobiologie, Immunologie und Hygiene, Universitätsklinikum Erlangen and Friedrich-Alexander Universität Erlangen-Nürnberg, D-91054 , Erlangen, Germany.
Asifa ZaidiPulmonary Diseases, Tulane Eosinophilic Disorder Center, Tulane University School of Medicine , New Orleans, LA, USA.
Parmesh DuttPulmonary Diseases, Tulane Eosinophilic Disorder Center, Tulane University School of Medicine , New Orleans, LA, USA.
Anil MishraPulmonary Diseases, Tulane Eosinophilic Disorder Center, Tulane University School of Medicine , New Orleans, LA, USA.
Tulane University · USCincinnati Children's Hospital Medical Center · USCase Western Reserve University · USUniversity of Cincinnati · US

Funding

Role of IL-15 in the Pathogensis of Eosinophilic EsophagitisR01AI080581 · NIAID · TULANE UNIVERSITY OF LOUISIANA · PI MISHRA, ANIL · 2009 to 2023
$4.9M
Mechanistic Analysis of Eosinophilic Esophagitis.R01DK067255 · NIDDK · TULANE UNIVERSITY OF LOUISIANA · PI MISHRA, ANIL · 2005 to 2014
$2.6M
NIAID NIH HHS R01 AI080581NIDDK NIH HHS R01 DK067255
6 · The paper itself

Abstract

Eosinophilic esophagitis (EoE) is a recently recognized inflammatory disorder that needs a potential therapeutic strategy. We earlier showed that iNKT cell-deficient mice are protected from allergen-induced EoE. Therefore, we now tested the hypothesis that iNKT cells are induced in the human EoE and is a novel possible target for the treatment of human EoE. Accordingly, we examine number of iNKT cells and eosinophils and expression of iNKT-associated cell surface receptors and chemokines by performing immunofluorescence, qPCR and ELISA in the esophageal biopsies and blood samples of normal subjects (comparison control) and EoE patients. Herein, we show that iNKT cell number, their receptor subcomponents Vα24 and Vβ11 expression, and associated chemokine CXCL16 levels (or expression) are induced significantly in EoE patients compared with normal individuals. In addition, we show that CXCL16 levels (or expression) correlate with the mRNA levels of Vα24 receptor but not well with esophageal eosinophilia in human EoE. Of note, we show that in vivo activation of iNKT cells is sufficient to induce EoE in mice. Furthermore, we show that anti-mCD1d- and anti-hVα24Jα18-neutralizing antibody treatment protects allergen-induced experimental EoE. Taken together, we have shown first time that iNKT cells have a critical pathogenic role in human and experimental EoE. iNKT cell neutralization by humanized anti-CD1d and anti-Vα24Jα18 antibodies might be a novel and potential therapy for human EoE.

Indexed as

anti-CD1danti-Vα24Jα18CXCL16iNKT cellsPBS57

Identifiers

PMID25505954
PMCPMC4232063
OpenAlexW1991718600

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.