Evidence map›Paper›PMID 34557196›Full record

ArticleFrontiers in immunology2021

Clinical Relevance of Serum Kyn/Trp Ratio and Basal and IFNγ-Upregulated IDO1 Expression in Peripheral Monocytes in Early Stage Melanoma.

Annabel Meireson, Liesbeth Ferdinande, Marc Haspeslagh, Benjamin Hennart, Delphine Allorge, Piet Ost, Nora Sundahl, Mathieu Spaas, Annelies Demeyer, Lieve Brochez

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 44% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Peptide-based vaccine for cancer therapies.Frontiers in immunology · 2023
    Review
  12. Review
  13. Article
  14. 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

10 authors at 4 institutions in 2 countries.

Annabel MeiresonCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Liesbeth FerdinandeDepartment of Pathology, Ghent University Hospital, Ghent, Belgium.
Marc HaspeslaghDermatology Research Unit, Ghent University Hospital, Ghent, Belgium.
Benjamin HennartLe Centre Hospitalier Universitaire de Lille (CHU), Unité Fonctionnelle de Toxicologie, Lille, France.
Delphine AllorgeLe Centre Hospitalier Universitaire de Lille (CHU), Unité Fonctionnelle de Toxicologie, Lille, France.
Piet OstCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Nora SundahlCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Mathieu SpaasCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Annelies DemeyerCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Lieve BrochezCancer Research Institute Ghent (CRIG), Ghent University, Ghent, Belgium.
Ghent University Hospital · BEUniversité de Lille · FRCancer Research Institute Ghent · BEGhent University · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune escape is an early phenomenon in cancer development/progression. Indoleamine 2,3-dioxygenase 1 (IDO1) is a normal endogenous mechanism of acquired peripheral immune tolerance and may therefore be tumor-promoting. This study investigated the clinical relevance of IDO1 expression by immune cells in the lymph nodes and blood and of the serum kynurenine/tryptophan (Kyn/Trp) ratio in 65 systemic treatment naïve stage I-III melanoma patients. Blood samples were collected within the first year of diagnosis. Patients had a median follow-up of 61 months. High basal IDO1 expression in peripheral monocytes and low IFNγ-induced IDO1 upregulation correlated with worse outcome independent from disease stage. Interestingly studied factors were not interrelated. During follow-up, the risk of relapse was 9% (2/22) in the subgroup with high IFNγ-induced IDO1 upregulation in monocytes. In contrast, if IDO1 upregulation was low, relapse occurred in 30% (3/10) of patients with low basal IDO1 expression in monocytes and in 61.5% (8/13) in the subgroup with high basal IDO1 expression in monocytes (Log-Rank test, p=0.008). This study reveals some immune features in the blood of early stage melanoma that may be of relevance for disease outcome. These may offer a target for sub-stratification and early intervention.

Indexed as

AdultCells, CulturedEnzyme InductionFemaleHumansIndoleamine-Pyrrole 2,3,-DioxygenaseInterferon-gammaKynurenineMaleMelanomaMiddle AgedMonocytesNeoplasm Recurrence, LocalNeoplasm StagingRetrospective StudiesSkin NeoplasmsIDO1 protein, humanIndoleamine-Pyrrole 2,3,-DioxygenaseInterferon-gammaKynurenineTryptophanbiomarkerearly stage melanomaIDO1immune cellsKyn/Trpliquid biopsymonocytestryptophan metabolism

Identifiers

PMID34557196
PMCPMC8453201
OpenAlexW3197246912

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.