Evidence map›Paper›PMID 35217577›Full record

ArticleJournal for immunotherapy of cancer2022

Tumor-specific T cells support chemokine-driven spatial organization of intratumoral immune microaggregates needed for long survival.

Ziena Abdulrahman, Saskia J Santegoets, Gregor Sturm, Pornpimol Charoentong, Marieke E Ijsselsteijn, Antonios Somarakis, Thomas Höllt, Francesca Finotello, Zlatko Trajanoski, Sylvia L van Egmond and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 35 citations in OpenAlex.

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  7. Current medicinal chemistry · 2025
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  13. [Clinicopathological characteristics of the CD8Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2024
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  15. CD4Cellular & molecular immunology · 2024
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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

14 authors at 3 institutions in 3 countries.

Ziena AbdulrahmanMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-9079-0293
Saskia J SantegoetsMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-2874-4402
Gregor SturmBiocenter, Institute of Bioinformatics, Medical University of Innsbruck, Innsbruck, Austria.
Pornpimol CharoentongMedical Oncology and National Center for Tumor diseases, University Hospital Heidelberg, German Cancer Research Center, Heidelberg, Germany.
Marieke E IjsselsteijnPathology, Leiden University Medical Center, Leiden, The Netherlands.
Antonios SomarakisRadiology, Leiden University Medical Center, Leiden, The Netherlands.
Thomas HölltRadiology, Leiden University Medical Center, Leiden, The Netherlands.
Francesca FinotelloBiocenter, Institute of Bioinformatics, Medical University of Innsbruck, Innsbruck, Austria.ORCID 0000-0003-0712-4658
Zlatko TrajanoskiMedical University of Innsbruck, Innsbruck, Austria.
Sylvia L van EgmondOtolaryngology, Leiden University Medical Center, Leiden, The Netherlands.
Dana A M MustafaPathology, Tumor Immuno-Pathology Laboratory, Leiden University Medical Center, Leiden, The Netherlands.
Marij J P Welters *Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Noel F C C de Miranda *Pathology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-6122-1024
Sjoerd H van der BurgMedical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands shvdburg@lumc.nl.ORCID 0000-0002-6556-0354
Leiden University Medical Center · NLInnsbruck Medical University · ATGerman Cancer Research Center · DE

Funding

Austrian Science Fund FWF T 974European Research Council 786295
6 · The paper itself

Abstract

backgroundThe composition of the tumor immune microenvironment (TIME) associated with good prognosis generally also predicts the success of immunotherapy, and both entail the presence of pre-existing tumor-specific T cells. Here, the blueprint of the TIME associated with such an ongoing tumor-specific T-cell response was dissected in a unique prospective oropharyngeal squamous cell carcinoma (OPSCC) cohort, in which tumor-specific tumor-infiltrating T cells were detected (immune responsiveness (IR

methodsA comprehensive multimodal, high-dimensional strategy was applied to dissect the TIME of treatment-naive IR

resultsIR

conclusionThe production of lymphoid cell attracting and organizing chemokines by tumor-specific T cells in IR

Indexed as

ChemokinesFemaleHumansMaleMonitoring, ImmunologicT-LymphocytesTumor MicroenvironmentChemokinesimmunotherapytumor microenvironment

Identifiers

PMID35217577
PMCPMC8883276
OpenAlexW4214558579

What OpenQuestion holds

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LicenceCC BY-NC
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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.