Evidence map›Paper›PMID 25769417›Full record

ArticleJournal of immunological methods2015

Isolation and cytokine analysis of lamina propria lymphocytes from mucosal biopsies of the human colon.

Rowann Bowcutt, Lisa B Malter, Lea Ann Chen, Martin J Wolff, Ian Robertson, Daniel B Rifkin, Michael Poles, Ilseug Cho, P'ng Loke

Open access · greenAbstract read
In one paragraph

Article in Journal of immunological methods, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

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  12. Gastrointestinal immune and microbiome changes during parenteral nutrition.American journal of physiology. Gastrointestinal and liver physiology · 2017
    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 1 institution in 1 country.

Rowann BowcuttDepartment of Microbiology, New York University School of Medicine, New York, NY 10010, USA.
Lisa B MalterDepartment of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, NY, USA.
Lea Ann ChenDepartment of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, NY, USA.
Martin J WolffDepartment of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, NY, USA.
Ian RobertsonDepartment of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.
Daniel B RifkinDepartment of Cell Biology, New York University School of Medicine, New York, NY 10016, USA.
Michael PolesDepartment of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, NY, USA.
Ilseug ChoDepartment of Medicine, Division of Gastroenterology, New York University School of Medicine, New York, NY, USA.
P'ng LokeDepartment of Microbiology, New York University School of Medicine, New York, NY 10010, USA. Electronic address: png.loke@nyumc.org.
New York University · US

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
NCI NIH HHS P30 CA016087
6 · The paper itself

Abstract

Much of our understanding of gut-microbial interactions has come from mouse models. Intestinal immunity is complex and a combination of host genetics and environmental factors play a significant role in regulating intestinal immunity. Due to this complexity, no mouse model to date gives a complete and accurate representation of human intestinal diseases, such as inflammatory bowel diseases. However, intestinal tissue from patients undergoing bowel resection reflects a condition of severe disease that has failed treatment; hence a more dynamic perspective of varying inflammatory states in IBD could be obtained through the analyses of pinch biopsy material. Here we describe our protocol for analyzing mucosal pinch biopsies collected predominantly during colonoscopies. We have optimized flow cytometry panels to analyze up to 8 cytokines produced by CD4+ and CD8+ cells, as well as for characterizing nuclear proteins and transcription factors such as Ki67 and Foxp3. Furthermore, we have optimized approaches to analyze the production of cytokines, including TGF-beta from direct ex vivo cultures of pinch biopsies and LPMCs isolated from biopsies. These approaches are part of our workflow to try and understand the role of the gut microbiota in complex and dynamic human intestinal diseases.

Indexed as

BiopsyCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesColitis, UlcerativeColonColonoscopyCrohn DiseaseCytokinesForkhead Transcription FactorsHumansIntestinal MucosaKi-67 AntigenMicrobiotaTransforming Growth Factor betaCytokinesForkhead Transcription FactorsFOXP3 protein, humanKi-67 AntigenTransforming Growth Factor betaBiopsiesCytokinesFlow cytometryLamina propria mononuclear cells

Identifiers

PMID25769417
PMCPMC4725193
OpenAlexW2034235748

What OpenQuestion holds

Textmetadata
LicenceTDM
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.