Evidence map›Paper›PMID 25272297›Full record

ArticleInternational journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists2014

Characterization of the immune cell repertoire in the normal fallopian tube.

Laura Ardighieri, Silvia Lonardi, Daniele Moratto, Fabio Facchetti, Ie-Ming Shih, William Vermi, Robert J Kurman

Open access · greenAbstract read
In one paragraph

Article in International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists, 2014. 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
0.8field-weighted citation impact, top 29% 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, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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 3 institutions in 2 countries.

Laura Ardighieri*Department of Molecular and Translational Medicine (L.A., S.L., F.F., W.V.) ‡Laboratory of Genetic Disorders of Childhood, "A Nocivelli" Institute for Molecular Medicine, Department of Pathology, Spedali Civili of Brescia, Brescia, Italy (D.M.) †Department of Pathology (L.A., I.-M.S., R.J.K.), Johns Hopkins University, Baltimore, Maryland ∥Department of Pathology and Immunology (W.V.), Washington University School of Medicine, Saint Louis, Missouri.
Silvia Lonardi
Daniele Moratto
Fabio Facchetti
Ie-Ming Shih
William Vermi
Robert J Kurman
Johns Hopkins University · USAltera (United States) · USMinistry of Education, Universities and Research · IT

Funding

Pathogenesis of Ovarian Serous Borderline TumorsR01CA116184 · NCI · JOHNS HOPKINS UNIVERSITY · PI KURMAN, ROBERT J. · 2007 to 2010
$1.2M
NCI NIH HHS R01 CA116184
6 · The paper itself

Abstract

Recent studies implicating the fallopian tube as the site of putative precursors of ovarian serous carcinoma, and the hypothesis that injury, inflammation, and repair of the ovarian surface epithelium at the time of ovulation, may be contributing factors to ovarian carcinogenesis, prompted us to undertake a comprehensive analysis of the immune cells in the normal fallopian tube. Accordingly, the aim of this study was to provide a baseline for future studies exploring the relationship of inflammation with the early events of ovarian carcinogenesis by characterizing the immune cell repertoire in 13 normal human fallopian tubes, combining digital microscopy of immunostained slides and flow cytometry of fresh single-cell suspensions, with a panel of markers that identify the most important adaptive and innate immune cells. We found that CD45(+) leukocytes are regularly observed in the fallopian tube and are mainly composed of CD163(+) macrophages, CD11c dendritic cells, and CD8(+) T cells. In addition, there are minor populations of CD56(+) NK cells, CD4(+) T cells, CD20(+) B cells, TCRγδ(+) T cells, and, among dendritic cells, CD207(Langerin)(+) Langerhans cells. The cellular mapping that we performed indicates that the local immune system in the human fallopian tube is composed of a mixture of innate and adaptive immune cells, many of which are recognized as playing a role in cancer immune surveillance. This local immune system could provide a first line of defense against early precancerous lesions and could potentially be exploited for immune-based therapies.

Indexed as

AdultAgedFallopian TubesFemaleFlow CytometryFluorescent Antibody TechniqueHumansImmunohistochemistryImmunophenotypingMiddle Aged

Identifiers

PMID25272297
PMCPMC4617751
OpenAlexW2004256605

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.