Evidence map›Paper›PMID 15999153›Full record

Trial reportPathology oncology research : POR2005

Tumor-infiltrating B cell immunoglobulin variable region gene usage in invasive ductal breast carcinoma.

Peter Simsa, Jean-Luc Teillaud, David I Stott, József Tóth, Beatrix Kotlan

Abstract readClinical TrialRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Pathology oncology research : POR, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. B Cells and Antibodies in Kawasaki Disease.International journal of molecular sciences · 2019
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. The immune microenvironment of human tumors: general significance and clinical impact.Cancer microenvironment : official journal of the International Cancer Microenvironment Society · 2013
    Article
  11. Tumor-infiltrating B cells come into vogue.World journal of gastroenterology · 2013
    Article
  12. 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

5 authors at 3 institutions in 3 countries.

Peter SimsaNational Medical Center, Institute of Haematology and Immunology, Budapest, H-1135, Hungary.
Jean-Luc Teillaud
David I Stott
József Tóth
Beatrix Kotlan
Inserm · FRNational Institute of Oncology · HUUniversity of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A major focus of tumor immunology is to reveal the potential role and capacity of immunocompetent cells found in different solid tumor tissues. The most abundant infiltrating cells (TIL), the T lymphocytes have been investigated in details concerning T-cell receptor usage and specificity. However, B cells have hardly been investigated in this respect, although high cellular B-cell infiltration has been correlated with improved patients' survival in some breast carcinomas. This led to our objectives to study variable region gene usage of the tumor-infiltrating B cells in different breast carcinoma types. By defining the immunoglobulin repertoire of the tumor-infiltrating B lymphocytes in the most common invasive ductal carcinoma (IDC) of the breast we compared it to the rare medullary breast carcinoma (MBC). After phenotyping infiltrating ductal carcinomas, B cells were obtained from tumor tissue by microdissection technique. Numerous rearranged TIL-B immunoglobulin heavy chain V genes (VH) were amplified, cloned, sequenced, and comparatively analyzed. Some characteristics were found for both breast carcinoma types. The immunoglobulins produced by TIL-B in ductal carcinoma are highly matured and oligoclonal. We conclude that Ig variable region gene usage reveals similar and distinguishable characteristics of TIL-B immunoglobulin repertoires, which are representative of the nature of the immune responses in invasive ductal and medullary breast carcinomas.

Indexed as

Genes, ImmunoglobulinB-LymphocytesBrain Stem NeoplasmsBreast NeoplasmsCarcinoma, Ductal, BreastGene Rearrangement, B-Lymphocyte, Heavy ChainHumansImmunoglobulin Variable RegionLymphocytes, Tumor-InfiltratingNeoplasm InvasivenessRetrospective StudiesImmunoglobulin Variable Region

Identifiers

PMID15999153
OpenAlexW2121332963

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.