Evidence map›Paper›PMID 31712432›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Long-term in vivo microscopy of CAR T cell dynamics during eradication of CNS lymphoma in mice.

Matthias Mulazzani, Simon P Fräßle, Iven von Mücke-Heim, Sigrid Langer, Xiaolan Zhou, Hellen Ishikawa-Ankerhold, Justin Leube, Wenlong Zhang, Sarah Dötsch, Mortimer Svec and 7 more

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
4.5field-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

69 citing papers in PubMed, 2 syntheses or guidelines pooled it, 99 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Review
  5. Article
  6. Article
  7. IL-7-mediated expansion of autologous lymphocytes increases CD8bioRxiv : the preprint server for biology · 2025
    Article
  8. Recent advances in non-invasiveBiomaterials science · 2025
    Review
  9. Review
  10. Strategies for Altering Delivery Technologies to Optimize CAR Therapy.International journal of molecular sciences · 2025
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Applications of Intravital Imaging in Cancer Immunotherapy.Bioengineering (Basel, Switzerland) · 2024
    Review
  18. Article
  19. Article
  20. Review

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Matthias MulazzaniDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany; matthias.mulazzani@med.uni-muenchen.de louisa.vonbaumgarten@med.uni-muenchen.de.
Simon P FräßleInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.
Iven von Mücke-HeimDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany.
Sigrid LangerDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany.
Xiaolan ZhouDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany.
Hellen Ishikawa-AnkerholdDepartment of Internal Medicine I, Ludwig Maximilians University, 81377 Munich, Germany.
Justin LeubeInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.
Wenlong ZhangDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany.
Sarah DötschInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.
Mortimer SvecInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.
Martina RudeliusInstitute of Pathology, Ludwig Maximilians University, 80337 Munich, Germany.
Martin DreylingDepartment of Internal Medicine III, Ludwig Maximilians University, 81377 Munich, Germany.
Michael von Bergwelt-BaildonDepartment of Internal Medicine III, Ludwig Maximilians University, 81377 Munich, Germany.
Andreas StraubeDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany.
Veit R BuchholzInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.
Dirk H BuschInstitute for Medical Microbiology, Immunology and Hygiene, Technical University of Munich, 81675 Munich, Germany.ORCID 0000-0001-8713-093X
Louisa von BaumgartenDepartment of Neurology, Ludwig Maximilians University, 81377 Munich, Germany; matthias.mulazzani@med.uni-muenchen.de louisa.vonbaumgarten@med.uni-muenchen.de.
Ludwig-Maximilians-Universität München · DEInstitute of Medical Microbiology and Hygiene · DEInstitute for Advanced Study · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T cells expressing anti-CD19 chimeric antigen receptors (CARs) demonstrate impressive efficacy in the treatment of systemic B cell malignancies, including B cell lymphoma. However, their effect on primary central nervous system lymphoma (PCNSL) is unknown. Additionally, the detailed cellular dynamics of CAR T cells during their antitumor reaction remain unclear, including their intratumoral infiltration depth, mobility, and persistence. Studying these processes in detail requires repeated intravital imaging of precisely defined tumor regions during weeks of tumor growth and regression. Here, we have combined a model of PCNSL with in vivo intracerebral 2-photon microscopy. Thereby, we were able to visualize intracranial PCNSL growth and therapeutic effects of CAR T cells longitudinally in the same animal over several weeks. Intravenous (i.v.) injection resulted in poor tumor infiltration of anti-CD19 CAR T cells and could not sufficiently control tumor growth. After intracerebral injection, however, anti-CD19 CAR T cells invaded deeply into the solid tumor, reduced tumor growth, and induced regression of PCNSL, which was associated with long-term survival. Intracerebral anti-CD19 CAR T cells entered the circulation and infiltrated distant, nondraining lymph nodes more efficiently than mock CAR T cells. After complete regression of tumors, anti-CD19 CAR T cells remained detectable intracranially and intravascularly for up to 159 d. Collectively, these results demonstrate the great potential of anti-CD19 CAR T cells for the treatment of PCNSL.

Indexed as

AnimalsAntigens, CD19Cell CountCell MovementCentral Nervous System NeoplasmsCytotoxicity, ImmunologicForkhead Transcription FactorsHumansImmunotherapy, AdoptiveInjections, IntravenousInjections, IntraventricularIntravital MicroscopyLymphomaMaleMice, Mutant StrainsNeoplasms, ExperimentalAntigens, CD19CD19 molecule, humanForkhead Transcription FactorsReceptors, Chimeric AntigenWhn protein2-photon microscopyCAR T cellsPCNSLtumor immunology

Identifiers

PMID31712432
PMCPMC6883823
OpenAlexW2986466575

What OpenQuestion holds

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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.