Evidence map›Paper›PMID 33537169›Full record

ArticleOncoimmunology2021

T cells expanded from renal cell carcinoma display tumor-specific CD137 expression but lack significant IFN-γ, TNF-α or IL-2 production.

Saskia D van Asten, Rosa de Groot, Marleen M van Loenen, Suzanne M Castenmiller, Jeroen de Jong, Kim Monkhorst, John B A G Haanen, Derk Amsen, Axel Bex, Robbert M Spaapen and 1 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Saskia D van AstenDepartment of Immunopathology, Sanquin Research, Amsterdam, The Netherlands.ORCID 0000-0001-6498-1176
Rosa de GrootLandsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-4070-0848
Marleen M van LoenenLandsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Suzanne M CastenmillerLandsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Jeroen de JongDepartment Of Pathology, The Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital (NKI-AvL), Amsterdam, The Netherlands.
Kim MonkhorstDepartment Of Pathology, The Netherlands Cancer Institute-Antoni Van Leeuwenhoek Hospital (NKI-AvL), Amsterdam, The Netherlands.
John B A G HaanenDepartment Of Medical Oncology, NKI-AvL, Amsterdam, The Netherlands.
Derk AmsenLandsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Axel BexDepartment Of Urology, NKI-AvL, Amsterdam, The Netherlands.
Robbert M SpaapenDepartment of Immunopathology, Sanquin Research, Amsterdam, The Netherlands.ORCID 0000-0002-1329-8606
Monika C WolkersLandsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-3242-1363
Sanquin · NLThe Netherlands Cancer Institute · NLRoyal Free London NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic renal cell carcinoma (RCC) has a poor prognosis. Recent advances have shown beneficial responses to immune checkpoint inhibitors, such as anti-PD-1/PD-L1 antibodies. As only a subset of RCC patients respond, alternative strategies should be explored. Patients refractory to anti-PD-1 therapy may benefit from autologous tumor-infiltrating lymphocyte (TIL) therapy. Even though efficient TIL expansion was reported from RCC lesions, it is not well established how many RCC TIL products are tumor-reactive, how well they produce pro-inflammatory cytokines in response to autologous tumors, and whether their response correlates with the presence of specific immune cells in the tumor lesions. We here compared the immune infiltrate composition of RCC lesions with that of autologous kidney tissue of 18 RCC patients. Tcell infiltrates were increased in the tumor lesions, and CD8

Indexed as

Carcinoma, Renal CellKidney NeoplasmsCD8-Positive T-LymphocytesCytotoxicity, ImmunologicHumansInterleukin-2Lymphocytes, Tumor-InfiltratingTumor Necrosis Factor Receptor Superfamily, Member 9Interleukin-2TNFRSF9 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 9CD137dysfunctional T cellsimmune compositionimmunotherapyRCCTIL therapy

Identifiers

PMID33537169
PMCPMC7833735
OpenAlexW3122333955

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.