Evidence map›Paper›PMID 26719303›Full record

ArticleGut2017

Dual role of tumour-infiltrating T helper 17 cells in human colorectal cancer.

F Amicarella, M G Muraro, C Hirt, E Cremonesi, E Padovan, V Mele, V Governa, J Han, X Huber, R A Droeser and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 124 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
124citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% 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

124 citing papers in PubMed, 1 synthesis or guideline pooled it, 178 citations in OpenAlex.

  1. Interleukin-17A mRNA Expression is Associated with the Prognosis of Patients with Colorectal Cancer: A Pooled Meta-Analysis.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2022
    Pooled it
  2. Trial
  3. γδ T cells in colorectal and liver cancer.Nature reviews. Gastroenterology & hepatology · 2026
    Review
  4. Review
  5. Review
  6. Contextualizing TNature reviews. Immunology · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. TScience advances · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Review

64 more citing papers are in PubMed but not listed here.

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

23 authors at 7 institutions in 2 countries.

F AmicarellaDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
M G MuraroDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
C HirtDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
E CremonesiDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
E PadovanDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
V MeleDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
V GovernaDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
J HanDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
X HuberDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
R A DroeserDepartment of General Surgery, University Hospital Basel, Basel, Switzerland.
M ZuberDepartment of Visceral Surgery, Kantonsspital Olten, Olten, Switzerland.
M AdaminaDepartment of Visceral Surgery, Kantonsspital St Gallen, St. Gallen, Switzerland.
M BolliDepartment of Visceral Surgery, St Claraspital, Basel, Switzerland.
R RossoDepartment of Visceral Surgery, Ospedale Civico Lugano, Lugano, Switzerland.
A LugliInstitute of Pathology, University of Bern, Bern, Switzerland.
I ZlobecInstitute of Pathology, University of Bern, Bern, Switzerland.
L TerraccianoInstitute of Pathology, University of Basel, Basel, Switzerland.
L TornilloInstitute of Pathology, University of Basel, Basel, Switzerland.
P ZajacDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
S Eppenberger-CastoriInstitute of Pathology, University of Basel, Basel, Switzerland.
F TrapaniInstitute of Pathology, University of Basel, Basel, Switzerland.
D OertliDepartment of General Surgery, University Hospital Basel, Basel, Switzerland.
G IezziDepartment of Biomedicine, Institute of Surgical Research, University of Basel, Basel, Switzerland.
University of Basel · CHUniversity Hospital of Basel · CHUniversity of Bern · CHKantonsschule Olten · CHKantonsspital St. Gallen · CHOspedale regionale di Lugano · CHSt. Claraspital · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe immune contexture predicts prognosis in human colorectal cancer (CRC). Whereas tumour-infiltrating CD8+ T cells and myeloid CD16+ myeloperoxidase (MPO)+ cells are associated with favourable clinical outcome, interleukin (IL)-17-producing cells have been reported to correlate with severe prognosis. However, their phenotypes and functions continue to be debated.

objectiveTo investigate clinical relevance, phenotypes and functional features of CRC-infiltrating, IL-17-producing cells.

methodsIL-17 staining was performed by immunohistochemistry on a tissue microarray including 1148 CRCs. Phenotypes of IL-17-producing cells were evaluated by flow cytometry on cell suspensions obtained by enzymatic digestion of clinical specimens. Functions of CRC-isolated, IL-17-producing cells were assessed by in vitro and in vivo experiments.

resultsIL-17+ infiltrates were not themselves predictive of an unfavourable clinical outcome, but correlated with infiltration by CD8+ T cells and CD16+ MPO+ neutrophils. Ex vivo analysis showed that tumour-infiltrating IL-17+ cells mostly consist of CD4+ T helper 17 (Th17) cells with multifaceted properties. Indeed, owing to IL-17 secretion, CRC-derived Th17 triggered the release of protumorigenic factors by tumour and tumour-associated stroma. However, on the other hand, they favoured recruitment of beneficial neutrophils through IL-8 secretion and, most importantly, they drove highly cytotoxic CCR5+CCR6+CD8+ T cells into tumour tissue, through CCL5 and CCL20 release. Consistent with these findings, the presence of intraepithelial, but not of stromal Th17 cells, positively correlated with improved survival.

conclusionsOur study shows the dual role played by tumour-infiltrating Th17 in CRC, thus advising caution when developing new IL-17/Th17 targeted treatments.

Indexed as

AdultAgedAged, 80 and overCD8-Positive T-LymphocytesChemokine CCL20Chemokine CCL5Chemokine CXCL10Chemokine CXCL9Colorectal NeoplasmsFemaleHT29 CellsHumansInterleukin-17Interleukin-8Lymphocytes, Tumor-InfiltratingMaleCCL20 protein, humanCCL5 protein, humanChemokine CCL20Chemokine CCL5Chemokine CXCL10Chemokine CXCL9CXCL10 protein, humanCXCL9 protein, humanInterleukin-17Interleukin-8PeroxidaseReceptors, IgGCANCER IMMUNOBIOLOGYCOLORECTAL CANCERIMMUNE RESPONSEINFLAMMATORY MEDIATORST LYMPHOCYTES

Identifiers

PMID26719303
PMCPMC5529969
OpenAlexW2267145743

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.