Evidence map›Paper›PMID 36914207›Full record

ArticleJournal for immunotherapy of cancer2023

Invasive margin tissue-resident macrophages of high CD163 expression impede responses to T cell-based immunotherapy.

Marit J van Elsas, Camilla Labrie, Anders Etzerodt, Pornpimol Charoentong, Jordi J C van Stigt Thans, Thorbald Van Hall, Sjoerd H van der Burg

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Observational
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  7. Immunity and Beyond: Emerging Roles of Monocytes and Macrophages in Cancer.Advances in experimental medicine and biology · 2026
    Review
  8. LGMNFrontiers in immunology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
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  15. Imaging of tumor-associated macrophage dynamics during immunotherapy using a CD163-specific nanobody-based immunotracer.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Review
  18. SPI1Journal for immunotherapy of cancer · 2024
    Article
  19. Article
  20. Review
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

7 authors at 3 institutions in 3 countries.

Marit J van ElsasDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-9955-6356
Camilla LabrieDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Anders EtzerodtDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-6757-2068
Pornpimol CharoentongDepartment of Medical Oncology, National Center for Tumor Diseases, University Hospital Heidelberg, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Jordi J C van Stigt ThansDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.
Thorbald Van HallDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-9115-558X
Sjoerd H van der BurgDepartment of Medical Oncology, Oncode Institute, Leiden University Medical Center, Leiden, The Netherlands shvdburg@lumc.nl.ORCID 0000-0002-6556-0354
Leiden University Medical Center · NLAarhus University · DKGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary and secondary resistance is a major hurdle in cancer immunotherapy. Therefore, a better understanding of the underlying mechanisms involved in immunotherapy resistance is of pivotal importance to improve therapy outcome.

methodHere, two mouse models with resistance against therapeutic vaccine-induced tumor regression were studied. Exploration of the tumor microenvironment by high dimensional flow cytometry in combination with therapeutic

resultsComparison of the tumor immune infiltrate during early and late regression revealed a change from tumor-rejecting toward tumor-promoting macrophages. In concert, a rapid exhaustion of tumor-infiltrating T cells was observed. Perturbation studies identified a small but discernible CD163

conclusionsIn this study, a small population of CD163

Indexed as

NeoplasmsT-LymphocytesAnimalsCD163 AntigenHumansImmunotherapyMacrophagesMiceTumor MicroenvironmentCD163 AntigenImmunotherapyMacrophagesTumor EscapeTumor Microenvironment

Identifiers

PMID36914207
PMCPMC10016286
OpenAlexW4324101878

What OpenQuestion holds

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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.