Evidence map›Paper›PMID 28806280›Full record

ArticleInflammatory bowel diseases2017

Integrated Analysis of Biopsies from Inflammatory Bowel Disease Patients Identifies SAA1 as a Link Between Mucosal Microbes with TH17 and TH22 Cells.

Mei San Tang, Rowann Bowcutt, Jacqueline M Leung, Martin J Wolff, Uma M Gundra, David Hudesman, Lisa B Malter, Michael A Poles, Lea Ann Chen, Zhiheng Pei and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Inflammatory bowel diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
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  3. CD74Journal of translational medicine · 2025
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  11. Mechanisms of Corticosteroid Resistance in Type 17 Asthma.Journal of immunology (Baltimore, Md. : 1950) · 2022
    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

17 authors at 4 institutions in 1 country.

Mei San Tang*Department of Microbiology, New York University School of Medicine, New York, New York; †Department of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, New York; ‡Department of Veterans Affairs, New York Harbor Healthcare System, New York, New York; §Department of Pathology, New York University School of Medicine, New York, New York; ‖Department of Medicine, Division of Gastroenterology, Mount Sinai School of Medicine, New York, New York; ¶Immunology Institute, Mount Sinai School of Medicine, New York, New York; **Department of Biology, Center for Genomics and Systems Biology, New York University, New York, New York; and ††Simons Center for Data Analysis, Simons Foundation, New York, New York.
Rowann Bowcutt
Jacqueline M Leung
Martin J Wolff
Uma M Gundra
David Hudesman
Lisa B Malter
Michael A Poles
Lea Ann Chen
Zhiheng Pei
Antonio G Neto
Wasif M Abidi
Thomas Ullman
Lloyd Mayer
Richard A Bonneau
Ilseung Cho
Pʼng Loke
Simons Foundation · USNew York University · USIcahn School of Medicine at Mount Sinai · USVA NY Harbor Healthcare System · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
THE ROLE OF ICSBP IN MUCOSAL IMMUNE RESPONSEP01DK072201 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HARPAZ, NOAM · 2006 to 2015
$14.6M
Modulation of innate immunity,microbiome and HIV transmission by Depo-ProveraR01AI110372 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI CHANG, THERESA L, YANG, LIYING · 2013 to 2017
$3.0M
Oral microbiome in esophageal adenocarcinomaU01CA182370 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AHN, JIYOUNG, PEI, ZHIHENG · 2014 to 2018
$2.7M
Regulation of vitamin A metabolism during Schistosoma mansoni infectionR01AI093811 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LOKE, PNG · 2011 to 2016
$2.4M
Role of Nod2 in preventing intestinal disease downstream of microbial imbalancesR01DK103788 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI CADWELL, KEN HASHIGIWA, LOKE, PNG · 2015 to 2017
$1.3M
Role of HPV in oral cavity squamous cell carcinomaR21DE025352 · NIDCR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PEI, ZHIHENG, YANG, LIYING · 2015 to 2016
$411k
NCI NIH HHS P30 CA016087NCI NIH HHS U01 CA182370NIAID NIH HHS R01 AI093811NIAID NIH HHS R01 AI110372NIDCR NIH HHS R21 DE025352NIDDK NIH HHS P01 DK072201NIDDK NIH HHS R01 DK103788
6 · The paper itself

Abstract

backgroundInflammatory bowel diseases (IBD) are believed to be driven by dysregulated interactions between the host and the gut microbiota. Our goal is to characterize and infer relationships between mucosal T cells, the host tissue environment, and microbial communities in patients with IBD who will serve as basis for mechanistic studies on human IBD.

methodsWe characterized mucosal CD4 T cells using flow cytometry, along with matching mucosal global gene expression and microbial communities data from 35 pinch biopsy samples from patients with IBD. We analyzed these data sets using an integrated framework to identify predictors of inflammatory states and then reproduced some of the putative relationships formed among these predictors by analyzing data from the pediatric RISK cohort.

resultsWe identified 26 predictors from our combined data set that were effective in distinguishing between regions of the intestine undergoing active inflammation and regions that were normal. Network analysis on these 26 predictors revealed SAA1 as the most connected node linking the abundance of the genus Bacteroides with the production of IL17 and IL22 by CD4 T cells. These SAA1-linked microbial and transcriptome interactions were further reproduced with data from the pediatric IBD RISK cohort.

conclusionsThis study identifies expression of SAA1 as an important link between mucosal T cells, microbial communities, and their tissue environment in patients with IBD. A combination of T cell effector function data, gene expression and microbial profiling can distinguish between intestinal inflammatory states in IBD regardless of disease types.

Indexed as

AdultBiopsyCase-Control StudiesCD4-Positive T-LymphocytesChildColonGastrointestinal MicrobiomeGene ExpressionHumansImmunity, CellularInflammatory Bowel DiseasesInterleukin-17Interleukin-22InterleukinsIntestinal MucosaSerum Amyloid A ProteinInterleukin-17Interleukin-22InterleukinsSAA1 protein, humanSerum Amyloid A Protein

Identifiers

PMID28806280
PMCPMC5613756
OpenAlexW2744747386

What OpenQuestion holds

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Registered trials

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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.