Evidence map›Paper›PMID 26155414›Full record

ArticleOncoimmunology2015

Accumulation of tolerogenic human 6-sulfo LacNAc dendritic cells in renal cell carcinoma is associated with poor prognosis.

Marieta Toma, Rebekka Wehner, Anja Kloß, Linda Hübner, Georgia Fodelianaki, Kati Erdmann, Susanne Füssel, Stefan Zastrow, Matthias Meinhardt, Barbara Seliger and 9 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Regulatory Effects of CD14Journal of immunology research · 2026
    Article
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  9. The immunology of renal cell carcinoma.Nature reviews. Nephrology · 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

19 authors at 10 institutions in 7 countries.

Marieta TomaInstitute of Pathology; University Hospital of Dresden ; Dresden, Germany.
Rebekka WehnerInstitute of Immunology; Medical Faculty; TU Dresden ; Dresden, Germany.
Anja KloßInstitute of Immunology; Medical Faculty; TU Dresden ; Dresden, Germany.
Linda HübnerInstitute of Immunology; Medical Faculty; TU Dresden ; Dresden, Germany.
Georgia FodelianakiInstitute of Immunology; Medical Faculty; TU Dresden ; Dresden, Germany ; Center for Regenerative Therapies Dresden ; Dresden, Germany.
Kati ErdmannDepartment of Urology; University Hospital of Dresden ; Dresden, Germany.
Susanne FüsselDepartment of Urology; University Hospital of Dresden ; Dresden, Germany.
Stefan ZastrowDepartment of Urology; University Hospital of Dresden ; Dresden, Germany.
Matthias MeinhardtInstitute of Pathology; University Hospital of Dresden ; Dresden, Germany.
Barbara SeligerInstitute for Medical Immunology; Martin Luther University Halle-Wittenberg ; Halle (Saale), Germany.
Dorothee BrechInstitute of Molecular Immunology; Helmholtz Center Munich; German Research Center for Environmental Health Munich ; Munich, Germany.
Elfriede NoessnerInstitute of Molecular Immunology; Helmholtz Center Munich; German Research Center for Environmental Health Munich ; Munich, Germany.
Torsten TonnCenter for Regenerative Therapies Dresden ; Dresden, Germany ; German Red Cross Blood Service ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany.
Knut SchäkelDepartment of Dermatology; University Hospital of Heidelberg ; Heidelberg, Germany.
Martin BornhäuserCenter for Regenerative Therapies Dresden ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany ; Department of Medicine I; University Hospital of Dresden ; Dresden, Germany.
Michael P BachmannCenter for Regenerative Therapies Dresden ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany ; Department of Radioimmunology; Institute of Radiopharmaceutical Cancer Research; Helmholtz Center Dresden-Rossendorf ; Dresden, Germany.
Manfred P WirthDepartment of Urology; University Hospital of Dresden ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany.
Gustavo BarettonInstitute of Pathology; University Hospital of Dresden ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany.
Marc SchmitzInstitute of Immunology; Medical Faculty; TU Dresden ; Dresden, Germany ; Center for Regenerative Therapies Dresden ; Dresden, Germany ; German Cancer Consortium (DKTK) ; Dresden, Germany ; German Cancer Research Center (DKFZ) ; Heidelberg, Germany.
German Cancer Research Center · DETechnische Universität Dresden · DETaipei Institute of Pathology · TWCenter for Environmental Health · USDeutschen Konsortium für Translationale Krebsforschung · DEFaculty (United Kingdom) · GBGerman Red Cross · DEHelmholtz Zentrum München · DELuther University · KRUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) essentially contribute to the induction and regulation of innate and adaptive immunity. Based on these important properties, DCs may profoundly influence tumor progression in patients. However, little is known about the role of distinct human DC subsets in primary tumors and their impact on clinical outcome. In the present study, we investigated the characteristics of human 6-sulfo LacNAc (slan) DCs in clear cell renal cell carcinoma (ccRCC). slanDCs have been shown to display various tumor-directed properties and to accumulate in tumor-draining lymph nodes from patients. When evaluating 263 ccRCC and 227 tumor-free tissue samples, we found increased frequencies of slanDCs in ccRCC tissues compared to tumor-free tissues. slanDCs were also detectable in the majority of 24 metastatic lymph nodes and 67 distant metastases from ccRCC patients. Remarkably, a higher density of slanDCs was significantly associated with a reduced progression-free, tumor-specific or overall survival of ccRCC patients. Tumor-infiltrating slanDCs displayed an immature phenotype expressing interleukin-10. ccRCC cells efficiently impaired slanDC-induced T-cell proliferation and programming as well as natural killer (NK) cell activation. In conclusion, these findings indicate that higher slanDC numbers in ccRCC tissues are associated with poor prognosis. The induction of a tolerogenic phenotype in slanDCs leading to an insufficient activation of innate and adaptive antitumor immunity may represent a novel immune escape mechanism of ccRCC. These observations may have implications for the design of therapeutic strategies that harness tumor-directed functional properties of DCs against ccRCC.

Indexed as

ccRCC, clear cell renal cell carcinomaCTLs, cytotoxic T cellsDCs, dendritic cellsdendritic cellsFCS, fetal calf serumHLA, human leukocyte antigenIFNγ, interferonγIL, interleukinILT, immunoglobulin-like transcriptLPS, lipopolysaccharideNK cells, natural killer cellsPBMCs, peripheral blood mononuclear cellsPMA, phorbol myristate acetaterenal cell carcinomaslan, 6-sulfo LacNAcT cellsTh1 cells, T helper type I cellsTMAs, tissue microarraysTNF-α, tumor necrosis factor-αtumor immunologytumor microenvironment

Identifiers

PMID26155414
PMCPMC4485722
OpenAlexW1860654126

What OpenQuestion holds

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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.