Evidence map›Paper›PMID 27140635›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

Aquaporin gene therapy corrects Sjögren's syndrome phenotype in mice.

Zhennan Lai, Hongen Yin, Javier Cabrera-Pérez, Maria C Guimaro, Sandra Afione, Drew G Michael, Patricia Glenton, Ankur Patel, William D Swaim, Changyu Zheng and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.9field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 97 citations in OpenAlex.

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  8. The Oral Microbial Ecosystem in Age-Related Xerostomia: A Critical Review.International journal of molecular sciences · 2024
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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.

Zhennan LaiAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892; Division of Biological Research on Drug Dependence, Department of Pharmaceutical Bioscience, Uppsala University, S-751 24 Uppsala, Sweden;
Hongen YinAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Javier Cabrera-PérezAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Maria C GuimaroAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Sandra AfioneAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Drew G MichaelAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Patricia GlentonDepartment of Pathology and Infectious Diseases, University of Florida, Gainesville, FL 32611.
Ankur PatelAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
William D SwaimAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Changyu ZhengAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892;
Cuong Q NguyenDepartment of Pathology and Infectious Diseases, University of Florida, Gainesville, FL 32611.
Fred NybergDivision of Biological Research on Drug Dependence, Department of Pharmaceutical Bioscience, Uppsala University, S-751 24 Uppsala, Sweden;
John A ChioriniAdeno-Associated Virus Biology Section, Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892; jchiorini@dir.nidcr.nih.gov.
National Institute of Dental and Craniofacial Research · USNational Institutes of Health · USUniversity of Florida · USUppsala University · SE

Funding

Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Adeno-associated Virus Biology And Utilization For Gene TransferZIADE000695 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI CHIORINI, JAY · 2009 to 2025
$36.6M
Adeno-associated Virus Biology And Utilization For Gene TransferZ01DE000695 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI CHIORINI, JOHN A · 2000 to 2008
$3.4M
Immuno-pathophysiology of Lymphocytic Foci in Sjogren?s SyndromeR00DE018958 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2011 to 2013
$717k
Massive analysis of paired TCR chains of TH17 cells in Sjogrens syndrome usingR21DE023433 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2014 to 2015
$393k
Immune-pathophysiology of lymphocytic foci in Sjogren's syndromeK99DE018958 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2009 to 2010
$216k
Intramural NIH HHS Z01 DE000695NCATS NIH HHS UL1 TR001427NIDCR NIH HHS K99 DE018958NIDCR NIH HHS R00 DE018958NIDCR NIH HHS R21 DE023433
6 · The paper itself

Abstract

Primary Sjögren's syndrome (pSS) is a chronic autoimmune disease that is estimated to affect 35 million people worldwide. Currently, no effective treatments exist for Sjögren's syndrome, and there is a limited understanding of the physiological mechanisms associated with xerostomia and hyposalivation. The present work revealed that aquaporin 5 expression, a water channel critical for salivary gland fluid secretion, is regulated by bone morphogenetic protein 6. Increased expression of this cytokine is strongly associated with the most common symptom of primary Sjögren's syndrome, the loss of salivary gland function. This finding led us to develop a therapy in the treatment of Sjögren's syndrome by increasing the water permeability of the gland to restore saliva flow. Our study demonstrates that the targeted increase of gland permeability not only resulted in the restoration of secretory gland function but also resolved the hallmark salivary gland inflammation and systemic inflammation associated with disease. Secretory function also increased in the lacrimal gland, suggesting this local therapy could treat the systemic symptoms associated with primary Sjögren's syndrome.

Indexed as

Genetic TherapyAdultAgedAnimalsAquaporin 1Aquaporin 5Bone Morphogenetic Protein 6Cell LineCell Membrane PermeabilityDown-RegulationFemaleGene SilencingHumansLacrimal ApparatusMaleMice, Inbred C57BLAQP1 protein, humanAQP5 protein, humanAquaporin 1Aquaporin 5BMP6 protein, humanBone Morphogenetic Protein 6Wateraquaporingene therapySjögren’s syndrome

Identifiers

PMID27140635
PMCPMC4878512
OpenAlexW2346257082

What OpenQuestion holds

Textmetadata
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.