Evidence map›Paper›PMID 35776791›Full record

ArticleScience advances2022

Immunotherapy of glioblastoma explants induces interferon-γ responses and spatial immune cell rearrangements in tumor center, but not periphery.

Tala Shekarian, Carl P Zinner, Ewelina M Bartoszek, Wandrille Duchemin, Anna T Wachnowicz, Sabrina Hogan, Manina M Etter, Julia Flammer, Chiara Paganetti, Tomas A Martins and 11 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 61 citations in OpenAlex.

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  19. Targeting PD-1 and CD85j can restore intratumoral CD4Journal for immunotherapy of cancer · 2025
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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

21 authors at 5 institutions in 2 countries.

Tala ShekarianBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-3964-5354
Carl P ZinnerBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0003-1609-0920
Ewelina M BartoszekBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0001-5153-9258
Wandrille DucheminsciCORE Center for Scientific Computing, University of Basel, Basel, Switzerland.ORCID 0000-0001-8854-7235
Anna T WachnowiczBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0001-7191-1969
Sabrina HoganBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0003-3994-8109
Manina M EtterBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-2889-8305
Julia FlammerBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.
Chiara PaganettiBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.
Tomas A MartinsBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0001-6016-2288
Philip SchmassmannBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-9411-3852
Steven ZanganehDepartment of Bioengineering, University of Massachusetts Dartmouth, Dartmouth, MA, USA.ORCID 0000-0002-6781-6456
Francois Le GoffIdorsia Pharmaceuticals Ltd., Allschwil, Switzerland.ORCID 0000-0002-8391-0602
Manuele G MuraroTissue Engineering Laboratory, Department of Biomedicine, University Hospital of Basel and University of Basel, Basel, Switzerland.ORCID 0000-0002-4590-1916
Marie-Françoise RitzBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.
Darci PhillipsDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-0804-3342
Salil S BhateDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-2057-9182
Graham L BarlowDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0001-9335-5414
Garry P NolanDepartment of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
Christian M SchürchDepartment of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.ORCID 0000-0002-1792-1768
Gregor HutterBrain Tumor Immunotherapy Lab, Department of Biomedicine, University of Basel, Basel, Switzerland.ORCID 0000-0002-7570-3902
University of Basel · CHStanford University · USIdorsia (Switzerland) · CHUniversity Hospital of Basel · CHUniversity of Massachusetts Dartmouth · US

Funding

MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Postgraduate Training Program in Epithelial BiologyT32AR007422 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1986 to 2026
$5.0M
Characterizing the immune and metabolic profiles of cutaneous T-cell lymphoma in formalin-fixed paraffin-embedded skin tissue samplesF32CA233203 · NCI · STANFORD UNIVERSITY · PI PHILLIPS, DARCI · 2018 to 2021
$183k
Cancer Research UK 27145NCI NIH HHS F32 CA233203NIAID NIH HHS T32 AI007290NIAMS NIH HHS T32 AR007422
6 · The paper itself

Abstract

A patient-tailored, ex vivo drug response platform for glioblastoma (GBM) would facilitate therapy planning, provide insights into treatment-induced mechanisms in the immune tumor microenvironment (iTME), and enable the discovery of biomarkers of response. We cultured regionally annotated GBM explants in perfusion bioreactors to assess iTME responses to immunotherapy. Explants were treated with anti-CD47, anti-PD-1, or their combination, and analyzed by multiplexed microscopy [CO-Detection by indEXing (CODEX)], enabling the spatially resolved identification of >850,000 single cells, accompanied by explant secretome interrogation. Center and periphery explants differed in their cell type and soluble factor composition, and responses to immunotherapy. A subset of explants displayed increased interferon-γ levels, which correlated with shifts in immune cell composition within specified tissue compartments. Our study demonstrates that ex vivo immunotherapy of GBM explants enables an active antitumoral immune response within the tumor center and provides a framework for multidimensional personalized assessment of tumor response to immunotherapy.

Identifiers

PMID35776791
PMCPMC10883360
OpenAlexW4283744811

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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.