Evidence map›Paper›PMID 41817579›Full record

ReviewCancer research2026

The Conflicting Role of Myeloid Cells in CAR T-Cell Therapy.

Grace DeFranco, Elizabeth L Siegler, Saad S Kenderian

Abstract readReview
In one paragraph

Review in Cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Coordinated expansion of CD163bioRxiv : the preprint server for biology · 2026
    Article
  2. Neurological complications of current and emerging CAR-T cell therapies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  3. 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

3 authors.

Grace DeFrancoT Cell Engineering, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-6037-9425
Elizabeth L SieglerT Cell Engineering, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0002-8336-4373
Saad S KenderianT Cell Engineering, Mayo Clinic, Rochester, Minnesota.ORCID 0000-0003-2767-3830

Funding

Towards Safer and More Effective CART Cell Therapy Through the Modulation of Myeloid CytokinesR37CA266344 · NCI · MAYO CLINIC ROCHESTER · PI Saad J. Kenderian · 2022 to 2026
$3.5M
Engineered Mesenchymal Stromal Cells for Enhanced ImmunosuppressionR01AI179974 · NIAID · MAYO CLINIC ROCHESTER · PI Saad J. Kenderian · 2024 to 2026
$2.4M
Center for Cancer Research (CCR) R37CA266344National Institute of Allergy and Infectious Diseases (NIAID) R01AI179974NCI NIH HHS R37 CA266344NIAID NIH HHS R01 AI179974
6 · The paper itself

Abstract

Chimeric antigen receptor T (CAR T)-cell therapy is revolutionizing cancer treatment in hematologic malignancies, but challenges related to the tumor microenvironment have hindered CAR T success, especially in solid tumors. Myeloid cells in particular have been implicated in CAR T efficacy. In this review, we discuss the roles of myeloid cells in CAR T-associated toxicities, including cytokine release syndrome, immune effector cell-associated neurotoxicity syndrome, and immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome, along with strategies to treat these toxicities by modulating myeloid cells. The review also explores myeloid cell-mediated suppression or enhancement of CAR T function. Finally, strategies used to target myeloid cells in combination with CAR T-cell therapy will be investigated.

Indexed as

Immunotherapy, AdoptiveMyeloid CellsNeoplasmsReceptors, Chimeric AntigenAnimalsCytokine Release SyndromeHumansLymphohistiocytosis, HemophagocyticT-LymphocytesTumor MicroenvironmentReceptors, Chimeric Antigen

Identifiers

PMID41817579
PMCPMC13084640

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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.