Evidence map›Paper›PMID 30804212›Full record

ArticleThe Journal of biological chemistry2019

Granulocyte-macrophage colony-stimulating factor inactivation in CAR T-cells prevents monocyte-dependent release of key cytokine release syndrome mediators.

Mohit Sachdeva, Philippe Duchateau, Stéphane Depil, Laurent Poirot, Julien Valton

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

97 citing papers in PubMed, 149 citations in OpenAlex.

  1. Article
  2. Review
  3. Macrophage Extracellular Traps in Immunity and Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. Review
  5. The neurotoxic legacy of CAR-T cells: where do we stand?Therapeutic advances in neurological disorders · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Novel strategies to manage CAR-T cell toxicity.Nature reviews. Drug discovery · 2025
    Review
  10. Review
  11. Deep insight into cytokine storm: from pathogenesis to treatment.Signal transduction and targeted therapy · 2025
    Review
  12. Review
  13. Article
  14. Perspective of usingFrontiers in immunology · 2025
    Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review

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

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

5 authors at 1 institution in 2 countries.

Mohit SachdevaFrom Cellectis, Inc., 430 East 29th St., New York, New York 10016 and mohit.sachdeva@cellectis.com.
Philippe DuchateauCellectis, 8 Rue de la Croix Jarry, 75013 Paris, France.
Stéphane DepilCellectis, 8 Rue de la Croix Jarry, 75013 Paris, France.
Laurent PoirotCellectis, 8 Rue de la Croix Jarry, 75013 Paris, France.
Julien ValtonFrom Cellectis, Inc., 430 East 29th St., New York, New York 10016 and julien.valton@cellectis.com.ORCID 0000-0003-0826-5401
Cellectis (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor T-cell (CAR T-cell) therapy has been shown to be clinically effective for managing a variety of hematological cancers. However, CAR T-cell therapy is associated with multiple adverse effects, including neurotoxicity and cytokine release syndrome (CRS). CRS arises from massive cytokine secretion and can be life-threatening, but it is typically managed with an anti-IL-6Ra mAb or glucocorticoid administration. However, these treatments add to a patient's medication burden and address only the CRS symptoms. Therefore, alternative strategies that can prevent CRS and neurotoxicity associated with CAR T-cell treatment are urgently needed. Here, we explored a therapeutic route aimed at preventing CRS rather than limiting its consequences. Using a cytokine-profiling assay, we show that granulocyte-macrophage colony-stimulating factor (GMCSF) is a key CRS-promoting protein. Through a combination of

Indexed as

Immunotherapy, AdoptiveMonocytesAntineoplastic Agents, ImmunologicalCytokinesGene EditingGene Knockdown TechniquesGlucocorticoidsGranulocyte-Macrophage Colony-Stimulating FactorHematologic NeoplasmsHumansNeoplasm ProteinsReceptors, Chimeric AntigenAntineoplastic Agents, ImmunologicalCytokinesGlucocorticoidsGranulocyte-Macrophage Colony-Stimulating FactorNeoplasm ProteinsReceptors, Chimeric Antigencancer therapyCAR T-cell therapycytokine release syndrome (CRS)gene knockoutgene transfergranulocyte–macrophage colony-stimulating factor (GMCSF)immunotherapyinterleukin signalingT-cell

Identifiers

PMID30804212
PMCPMC6462525
OpenAlexW2917856590

What OpenQuestion holds

Textmetadata
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.