Evidence map›Paper›PMID 15479683›Full record

ArticleGut2004

Divergent cell cycle kinetics underlie the distinct functional capacity of mucosal T cells in Crohn's disease and ulcerative colitis.

A Sturm, A Z A Leite, S Danese, K A Krivacic, G A West, S Mohr, J W Jacobberger, C Fiocchi

Open access · bronzeAbstract read
In one paragraph

Article in Gut, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Evaluation of anFrontiers in microbiology · 2021
    Article
  5. Apoptosis in peripheral blood lymphocytes in intestinal tuberculosis and Crohn's disease: Implications to diagnostic differentiation.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Immunopathogenesis of IBD: current state of the art.Nature reviews. Gastroenterology & hepatology · 2016
    Review
  11. Article
  12. Article
  13. Role of DOR-β-arrestin1-Bcl2 signal transduction pathway and intervention effects of oxymatrine in ulcerative colitis.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2014
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

A SturmDepartment of Medicine, University Hospitals of Cleveland, Case Western Reserve University School of Medicine (BRB 425), 10900 Euclid Ave, Cleveland, Ohio, 44106-4952, USA.
A Z A Leite
S Danese
K A Krivacic
G A West
S Mohr
J W Jacobberger
C Fiocchi
University Hospitals of Cleveland · USCharité - Universitätsmedizin Berlin · DE

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Drew James Adams · 1987 to 2026
$142.3M
MUCOSAL LYMPHOKINES IN INFLAMMATORY BOWEL DISEASER37DK030399 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI FIOCCHI, CLAUDIO · 1999 to 2008
$3.2M
Cell interactions in the inflammed intestinal mucosaR01DK050984 · NIDDK · CLEVELAND CLINIC LERNER COM-CWRU · PI FIOCCHI, CLAUDIO · 1995 to 2014
$3.1M
STANDARDIZED MULTIPARAMETRIC CELL CYCLE ANALYSISR01CA073413 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI JACOBBERGER, JAMES W · 1996 to 2008
$2.4M
MUCOSAL LYMPHOKINES IN INFLAMMATORY BOWEL DISEASER01DK030399 · NIDDK · CLEVELAND CLINIC FOUNDATION · PI FIOCCHI, CLAUDIO · 1986 to 1997
–
NCI NIH HHS CA43703NCI NIH HHS CA73413NCI NIH HHS P30 CA043703NCI NIH HHS R01 CA073413NIDDK NIH HHS DK30399NIDDK NIH HHS DK50984NIDDK NIH HHS R01 DK050984NIDDK NIH HHS R37 DK030399
6 · The paper itself

Abstract

backgroundDifferent abnormalities of T cell effector function distinguish Crohn's disease (CD) from ulcerative colitis (UC). Because cell cycling determines effector function, pathogenic events in CD and UC may depend on cell cycle changes unique to each condition.

methodsCell cycle kinetics, cycle regulatory molecule expression, apoptosis, caspase and telomerase activity, and cellular expansion were evaluated in CD2 and CD3 activated control, CD, and UC lamina propria T cells.

resultsCompared with normal cells, CD T cells cycle faster, express increased phosphorylated Rb and decreased phosphorylated p53 levels, display less caspase activity but more telomerase activity, die less, and undergo vigorous cellular expansion. In contrast, UC T cells cycle slower, express normal levels of phosphorylated Rb and p53, display more caspase activity but have no telomerase activity, die more, and have a limited capacity to expand.

conclusionsT cell cycle abnormalities in CD indicate a state of hyperreactivity compatible with loss of tolerance, but a hyporeactive state compatible with anergy in UC. Thus distinct and divergent T cell cycle characteristics underlie the pathogenesis of the two main forms of inflammatory bowel disease.

Indexed as

AdolescentAdultAgedApoptosisCell CycleCell Cycle ProteinsCell DivisionCells, CulturedColitis, UlcerativeCrohn DiseaseFemaleFlow CytometryHumansImmunity, MucosalIntestinal MucosaLymphocyte ActivationCell Cycle Proteins

Identifiers

PMID15479683
PMCPMC1774268
OpenAlexW2073606800

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.