Evidence map›Paper›PMID 36626228›Full record

ArticleJCI insight2023

Cellular mechanisms and effects of IL-4 receptor blockade in experimental conjunctivitis evoked by skin inflammation.

Hongwei Han, Sheila Cummings, Kai-Ting C Shade, Jennifer Johnson, George Qian, Joseph Gans, Srinivas Shankara, Javier Escobedo, Erik Zarazinski, Renee Bodinizzo and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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  4. Review
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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

13 authors at 4 institutions in 2 countries.

Hongwei HanSanofi, Immunology and Inflammation Research Therapeutic Area, Cambridge, Massachusetts, USA.
Sheila CummingsSanofi, Global Discovery Pathology, Translational In-vivo Models Platform, Cambridge, Massachusetts, USA.
Kai-Ting C ShadeSanofi, Immunology and Inflammation Research Therapeutic Area, Cambridge, Massachusetts, USA.
Jennifer JohnsonSanofi, Global Discovery Pathology, Translational In-vivo Models Platform, Cambridge, Massachusetts, USA.
George QianSanofi, Immunology and Inflammation Research Therapeutic Area, Cambridge, Massachusetts, USA.
Joseph GansSanofi, Translational Science Single Cell & Functional Genomics, Cambridge, Massachusetts, USA.
Srinivas ShankaraSanofi, Translational Science Single Cell & Functional Genomics, Cambridge, Massachusetts, USA.
Javier EscobedoSanofi, Translational Science Single Cell & Functional Genomics, Cambridge, Massachusetts, USA.
Erik ZarazinskiSanofi, In-vivo Research Center, Translational In-vivo Models Platform, Cambridge, Massachusetts, USA.
Renee BodinizzoSanofi, In-vivo Research Center, Translational In-vivo Models Platform, Cambridge, Massachusetts, USA.
Dinesh BangariSanofi, Global Discovery Pathology, Translational In-vivo Models Platform, Cambridge, Massachusetts, USA.
Paul BryceSanofi, Immunology and Inflammation Research Therapeutic Area, Cambridge, Massachusetts, USA.
Alexandra HicksSanofi, Immunology and Inflammation Research Therapeutic Area, Cambridge, Massachusetts, USA.
Inflammation Research Foundation · USID Genomics (United States) · USSanofi (France) · FRVietnamese Voluntary Foundation · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ocular surface diseases, including conjunctivitis, are recognized as common comorbidities in atopic dermatitis (AD) and occur at an increased frequency in patients with AD treated with biologics targeting IL-4 receptor α (IL-4Rα) or IL-13. However, the inflammatory mechanisms underlying this pathology are unknown. Here, we developed a potentially novel mouse model of skin inflammation-evoked conjunctivitis and showed that it is dependent on CD4+ T cells and basophils. Blockade of IL-4Rα partially attenuated conjunctivitis development, downregulated basophil activation, and led to a reduction in expression of genes related to type 2 cytokine responses. Together, these data suggest that an IL-4Rα/basophil axis plays a role in the development of murine allergic conjunctivitis. Interestingly, we found a significant augmentation of a number of genes that encode tear proteins and enzymes in anti-IL-4Rα-treated mice, and it may underlie the partial efficacy in this model and may represent candidate mediators of the increased frequency of conjunctivitis following dupilumab in patients with AD.

Indexed as

ConjunctivitisDermatitis, AtopicAnimalsCytokinesInflammationInterleukin-4 Receptor alpha SubunitMiceReceptors, Interleukin-4CytokinesIl4ra protein, mouseInterleukin-4 Receptor alpha SubunitReceptors, Interleukin-4BasophilsCytokinesDermatologyImmunologyMouse models

Identifiers

PMID36626228
PMCPMC9977427
OpenAlexW4315436475

What OpenQuestion holds

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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 OpenQuestion graph.