Evidence map›Paper›PMID 27526715›Full record

ArticleThe Journal of experimental medicine2016

Carbonic anhydrase enzymes regulate mast cell-mediated inflammation.

Everett K Henry, Chandler B Sy, Juan M Inclan-Rico, Vanessa Espinosa, Saleena S Ghanny, Daniel F Dwyer, Patricia Soteropoulos, Amariliz Rivera, Mark C Siracusa

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
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  6. Mechanisms of pulmonary vascular dysfunction in pulmonary hypertension and implications for novel therapies.American journal of physiology. Heart and circulatory physiology · 2022
    Review
  7. Article
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  14. Carbonic Anhydrase Inhibition Ameliorates Inflammation and Experimental Pulmonary Hypertension.American journal of respiratory cell and molecular biology · 2019
    Article
  15. Review
  16. Article
  17. 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

9 authors at 2 institutions in 1 country.

Everett K HenryCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Medicine, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-3884-2612
Chandler B SyCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Medicine, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-8739-561X
Juan M Inclan-RicoCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Medicine, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0003-1134-9139
Vanessa EspinosaCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Pediatrics, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0003-4808-3557
Saleena S GhannyThe Genomics Center, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0001-6922-1862
Daniel F DwyerDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA 02115 Harvard Medical School, Boston, MA 02115.ORCID 0000-0001-5029-261X
Patricia SoteropoulosThe Genomics Center, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Microbiology, Biochemistry, and Molecular Genetics, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.
Amariliz RiveraCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Pediatrics, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103.ORCID 0000-0002-2173-5597
Mark C SiracusaCenter for Immunity and Inflammation, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 Department of Medicine, New Jersey Medical School, Rutgers, The State University of New Jersey, Newark, NJ 07103 mark.siracusa@rutgers.edu.ORCID 0000-0003-3499-5408
Rutgers, The State University of New Jersey · USBrigham and Women's Hospital · US

Funding

Innate Immune regulation of helminth-induced inflammationR01AI123224 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SIRACUSA, MARK CHRISTOPHER · 2016 to 2020
$2.0M
Regulation of antifungal immunity by monocyte-derived dendritic cellsR01AI114647 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI RIVERA, AMARILIZ · 2015 to 2019
$1.8M
Interrogating innate immunity to helminth parasitesK22AI110573 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI SIRACUSA, MARK CHRISTOPHER · 2015 to 2016
$270k
NIAID NIH HHS K22 AI110573NIAID NIH HHS R01 AI114647NIAID NIH HHS R01 AI123224
6 · The paper itself

Abstract

Type 2 cytokine responses are necessary for the development of protective immunity to helminth parasites but also cause the inflammation associated with allergies and asthma. Recent studies have found that peripheral hematopoietic progenitor cells contribute to type 2 cytokine-mediated inflammation through their enhanced ability to develop into mast cells. In this study, we show that carbonic anhydrase (Car) enzymes are up-regulated in type 2-associated progenitor cells and demonstrate that Car enzyme inhibition is sufficient to prevent mouse mast cell responses and inflammation after Trichinella spiralis infection or the induction of food allergy-like disease. Further, we used CRISPR/Cas9 technology and illustrate that genetically editing Car1 is sufficient to selectively reduce mast cell development. Finally, we demonstrate that Car enzymes can be targeted to prevent human mast cell development. Collectively, these experiments identify a previously unrecognized role for Car enzymes in regulating mast cell lineage commitment and suggest that Car enzyme inhibitors may possess therapeutic potential that can be used to treat mast cell-mediated inflammation.

Indexed as

AnimalsCarbonic Anhydrase InhibitorsCarbonic AnhydrasesImmunoglobulin EInflammationMast CellsMastocytosisMethazolamideMiceMice, Inbred C57BLCarbonic Anhydrase InhibitorsCarbonic AnhydrasesImmunoglobulin EMethazolamide

Identifiers

PMID27526715
PMCPMC4995079
OpenAlexW2516341338

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.