Evidence map›Paper›PMID 18453619›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Functional Th1 cells are required for surgical adhesion formation in a murine model.

Arthur O Tzianabos, Matthew A Holsti, Xin-Xiao Zheng, Arthur F Stucchi, Vijay K Kuchroo, Terry B Strom, Laurie H Glimcher, William W Cruikshank

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

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  14. Animal models of intestinal fibrosis: new tools for the understanding of pathogenesis and therapy of human disease.American journal of physiology. Gastrointestinal and liver physiology · 2012
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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

8 authors at 5 institutions in 1 country.

Arthur O Tzianabos *Department of Medicine and Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Matthew A Holsti *Department of Medicine and Channing Laboratory, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Xin-Xiao ZhengDivision of Immunology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115.
Arthur F StucchiDepartment of Surgery, Boston University Medical Center, Boston, MA 02118.
Vijay K KuchrooCenter for Neurologic Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115.
Terry B StromDivision of Immunology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02115.
Laurie H GlimcherHarvard School of Public Health and Harvard Medical School, Boston, MA 02115.
William W CruikshankPulmonary Center, Boston University School of Medicine, Boston, MA 02118.
Brigham and Women's Hospital · USBeth Israel Deaconess Medical Center · USBoston Medical Center · USBoston University · USHarvard University · US

Funding

Transgenic / Knock-out mouse coreP01AI073748 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BEHAR, SAMUEL M · 2008 to 2019
$17.1M
T-bet and Tumor ImmunityR01CA112663 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GLIMCHER, LAURIE HOLLIS · 2005 to 2015
$3.3M
INTERLEUKIN REGULATION OF CD4+ T CELLS IN LUNG DISEASESR01HL032802 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M · 1985 to 2003
$1.4M
NCI NIH HHS CA 112663NCI NIH HHS R01 CA112663NHLBI NIH HHS HL 32802NHLBI NIH HHS R01 HL032802NIAID NIH HHS P01 AI073748RMOD NIH HHS RM 64805-01
6 · The paper itself

Abstract

Tissue trauma in the peritoneal and pelvic cavities following surgery or bacterial infection results in adhesions that are a debilitating cause of intestinal obstruction, chronic pelvic pain, and infertility in women. We recently demonstrated that CD4(+) alphabeta T cells are essential for development of this process. Using a murine model of experimental adhesion formation, we now demonstrate that adhesion formation is characterized by the selective recruitment of Tim-3(+), CCR5(+), CXCR3(+), IFN-gamma(+) cells, indicating the presence of a Th1 phenotype. We further demonstrate that adhesion formation is critically dependent on the function of Th1 cells because mice genetically deficient for IFN-gamma, T-bet, or treated with Abs to the Th1-selective chemoattractant IL-16 show significantly less adhesion formation than wild-type mice. In addition, disrupting the interaction of the Th1-specific regulatory molecule Tim-3, with its ligand, significantly exacerbates adhesion formation. This enhanced response is associated with increases in the level of neutrophil-attracting chemokines KC and MIP-2, known to play a role in adhesiogenesis. These data demonstrate that the CD4(+) T cells orchestrating adhesion formation are of the Th1 phenotype and delineate the central role of T-bet, Tim-3, IFN-gamma, and IL-16 in mediating this pathogenic tissue response.

Indexed as

Postoperative ComplicationsAnimalsCytokinesDisease Models, AnimalEnzyme-Linked Immunosorbent AssayHepatitis A Virus Cellular Receptor 2Interferon-gammaInterleukin-16MiceReceptors, VirusT-bet Transcription FactorT-Box Domain ProteinsTh1 CellsTissue AdhesionsCytokinesHavcr2 protein, mouseHepatitis A Virus Cellular Receptor 2Interferon-gammaInterleukin-16Receptors, VirusT-bet Transcription FactorT-Box Domain Proteins

Identifiers

PMID18453619
PMCPMC3832137
OpenAlexW1937841653

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.