Evidence map›Paper›PMID 32875568›Full record

ArticleInternational journal of cancer2021

Interleukin-6-mediated resistance to immunotherapy is linked to impaired myeloid cell function.

Elham Beyranvand Nejad, Camilla Labrie, Tetje C van der Sluis, Suzanne van Duikeren, Kees L M C Franken, Rueshandra Roosenhoff, Ramon Arens, Thorbald van Hall, Sjoerd H van der Burg

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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  2. A baseline systemic inflammatory signature predicts anti-PD-1 response in advanced melanoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

9 authors at 1 institution in 1 country.

Elham Beyranvand NejadDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-9801-1351
Camilla LabrieDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Tetje C van der SluisDepartment of Immunology, Leiden University Medical Center, Leiden University Medical Center, Leiden, The Netherlands.
Suzanne van DuikerenDepartment of Immunology, Leiden University Medical Center, Leiden University Medical Center, Leiden, The Netherlands.
Kees L M C FrankenDepartment of Immunology, Leiden University Medical Center, Leiden University Medical Center, Leiden, The Netherlands.
Rueshandra RoosenhoffDepartment of Immunology, Leiden University Medical Center, Leiden University Medical Center, Leiden, The Netherlands.
Ramon ArensDepartment of Immunology, Leiden University Medical Center, Leiden University Medical Center, Leiden, The Netherlands.
Thorbald van HallDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Sjoerd H van der BurgDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-6556-0354
Leiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High serum levels of interleukin-6 (IL-6) correlate with poor prognosis and chemotherapy resistance in several cancers. The underlying mechanisms and its effects on immunotherapy are largely unknown. To address this, we developed a human papillomavirus type 16 (HPV16)-associated tumor model expressing IL-6 to investigate the impact of tumor-expressed IL-6 during cisplatin chemotherapy and HPV16 synthetic long peptide vaccination as immunotherapy. The effects of tumor-produced IL-6 on tumor growth, survival and the tumor microenvironment were analyzed. Our data demonstrated that tumor-produced IL-6 conferred resistance to cisplatin and therapeutic vaccination. This was not caused by a changed in vitro or in vivo growth rate of tumor cells, or a changed sensitivity of tumor cells to chemotherapy or T-cell-mediated killing. Furthermore, no overt differences in the frequencies of tumor-infiltrating subsets of T cells or CD11b

Indexed as

AnimalsCancer VaccinesCell Line, TumorCisplatinDisease Models, AnimalDrug Resistance, NeoplasmFemaleHistocompatibility Antigens Class IIHuman papillomavirus 16HumansImmunotherapyInterleukin-6MiceMyeloid CellsNeoplasmsPapillomavirus InfectionsCancer VaccinesCisplatinHistocompatibility Antigens Class IIInterleukin-6interleukin-6, mouseVaccines, Subunitchemotherapyimmunotherapyinterleukin-6tumor microenvironment

Identifiers

PMID32875568
PMCPMC7693233
OpenAlexW3082472856

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.