Evidence map›Paper›PMID 29060923›Full record

ArticleCancer biomarkers : section A of Disease markers2017

Infiltration of γ⁢δ T cells, IL-17+ T cells and FoxP3+ T cells in human breast cancer.

Roni Allaoui, Catharina Hagerling, Eva Desmond, Carl-Fredrik Warfvinge, Karin Jirström, Karin Leandersson

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
1.1field-weighted citation impact, top 23% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 35 citations in OpenAlex.

  1. Pooled it
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  12. A Metabolic Gene Signature to Predict Breast Cancer Prognosis.Frontiers in molecular biosciences · 2022
    Article
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  16. The Multifaceted Nature of Tumor Microenvironment in Breast Carcinomas.Pathobiology : journal of immunopathology, molecular and cellular biology · 2020
    Review
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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

6 authors at 1 institution in 1 country.

Roni AllaouiCancer Immunology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Catharina HagerlingCancer Immunology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Eva DesmondCancer Immunology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Carl-Fredrik WarfvingeDepartment of Clinical Sciences Lund, Oncology and Pathology, Lund University, Lund, Sweden.
Karin JirströmDepartment of Clinical Sciences Lund, Oncology and Pathology, Lund University, Lund, Sweden.
Karin LeanderssonCancer Immunology, Department of Translational Medicine, Lund University, Malmö, Sweden.
Lund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor-infiltrating lymphocytes (TILs) have a strong prognostic value in various forms of cancers. These data often refer to use of the pan-T cell marker CD3, or the cytotoxic T lymphocyte marker CD8α. However, T cells are a heterogeneous group of cells with a wide array of effector mechanisms ranging from immunosuppression to cytotoxicity.

objectiveIn this study we have investigated the prognostic effects of some unconventional T cell subtypes in breast cancer; γ⁢δ T cells, IL-17+ T cells and FoxP3+ T cells (Tregs) in relation to the conventional CD3 and CD8α T cell markers.

methodsThis was done using immunohistochemistry on a human breast cancer tissue microarray consisting of 498 consecutive cases of primary breast cancer.

resultsInfiltration of γ⁢δ T cells and T cell infiltration in general (CD3), correlated with a good prognosis, while Treg infiltration with a worse. Infiltration of γ⁢δ T cells was associated with a significantly improved clinical outcome in all breast cancer subtypes except triple negative tumors. Only infiltration of either CD3+ or CD8α+ cells was independently associated with better prognosis for all breast cancer patients.

conclusionsThis study sheds further light on the prognostic impact of various T cell subtypes in breast cancer.

Indexed as

Antineoplastic Agents, HormonalBreast NeoplasmsChemotherapy, AdjuvantDisease-Free SurvivalFemaleForkhead Transcription FactorsHumansKaplan-Meier EstimateLymphocytes, Tumor-InfiltratingMiddle AgedMultivariate AnalysisProportional Hazards ModelsReceptors, IgGTh17 CellsAntineoplastic Agents, HormonalForkhead Transcription FactorsFOXP3 protein, humanReceptors, IgGBreast cancerprognosisTILsT lymphocytesunconventional T cells

Identifiers

PMID29060923
PMCPMC5814667
OpenAlexW2766675494

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.