Evidence map›Paper›PMID 25978359›Full record

ArticlePloS one2015

The Involvement of Immune Semaphorins in the Pathogenesis of Inflammatory Bowel Diseases (IBDs).

Zahava Vadasz, Tova Rainis, Afif Nakhleh, Tharwat Haj, Jacob Bejar, Katty Halasz, Elias Toubi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. The Involvement of Semaphorins in the Pathogenesis of Skin Diseases.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Neuroimmune semaphorins as costimulatory molecules and beyond.Molecular medicine (Cambridge, Mass.) · 2018
    Review
  10. Review
  11. Article
  12. Guidance Molecules in Vascular Smooth Muscle.Frontiers in physiology · 2018
    Review
  13. Semaphorins 4A and 4D in chronic inflammatory diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  14. Article
  15. Review
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

7 authors at 1 institution in 1 country.

Zahava VadaszDivision of Allergy and Clinical Immunology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Tova RainisDivision of Gastroenterology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Afif NakhlehDivision of Allergy and Clinical Immunology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Tharwat HajDivision of Allergy and Clinical Immunology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Jacob BejarDepartment of Pathology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Katty HalaszDivision of Allergy and Clinical Immunology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Elias ToubiDivision of Allergy and Clinical Immunology, Bnai Zion Medical Center, Technion, Haifa, Israel.
Bnai Zion Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsImmune semaphorins are a large family of proteins involved in the pathogenesis of inflammatory diseases through the regulation of immune homeostasis and tissue inflammation. We aim to assess the possible involvement of semaphorin3A (sema3A) and 4A (sema4A) in peripheral immune responses and bowel tissue inflammation of patients suffering from Crohn's disease (CD) and ulcerative colitis (UC). PATIENTS AND

methodsTwenty-seven CD patients and 10 UC patients were studied and compared to 10 patients followed for acute diverticulitis (disease control) and 12 healthy individuals. All were evaluated for sema3A expression on T regulatory cells (Tregs), serum levels of sema3A and sema4A, and tissue expression of sema3A and sema4A in bowel biopsies.

resultsThe percentage (%) of T regulatory cells (Tregs) expressing sema3A in patients with active CD (64.5% ± 14.49%) and active UC (49.8% ± 16.45%) was significantly lower when compared to that of healthy controls (88.7% ± 3.6%, p< 0.001 and p< 0.0001, respectively). This expression was seen to be in negative correlation with CD activity. Serum levels of Sema4A were significantly lower in patients with CD and UC when compared to that of controls (5.69 ± 1 .48 ng\ml for CD, 5.26 ± 1.23 ng/ml for UC patients vs 9.74 ± 2.73 ng/ml for normal controls, P<0.001). Sema4A was highly expressed in lymphocytes of the lamina propria of CD and UC patients but absent in patients with diverticulitis or in normal individuals.

conclusionsAltered % of Tregs expressing sema3A in patients with inflammatory bowel diseases (IBD) is partially responsible for their failure in preventing CD4+ effector T cell induced inflammation in IBD in peripheral blood. The increased expression of sema4A in bowel biopsies from CD and UC patients is suggestive of its central role in regulating local tissue inflammation in the bowel.

Indexed as

AdultAgedCase-Control StudiesColitis, UlcerativeCrohn DiseaseFemaleHumansImmunohistochemistryMaleMiddle AgedSemaphorin-3ASemaphorinsT-Lymphocytes, RegulatoryYoung AdultSEMA3A protein, humanSEMA4A protein, humanSemaphorin-3ASemaphorins

Identifiers

PMID25978359
PMCPMC4433250
OpenAlexW1576171104

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.