Evidence map›Paper›PMID 36095236›Full record

ArticleCancer immunology research2022

Targeting Macrophages with CAR T Cells Delays Solid Tumor Progression and Enhances Antitumor Immunity.

Alfonso R Sánchez-Paulete, Jaime Mateus-Tique, Gurkan Mollaoglu, Sebastian R Nielsen, Adam Marks, Ashwitha Lakshmi, Jalal A Khan, C Matthias Wilk, Luisanna Pia, Alessia Baccarini and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
8.1field-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

75 citing papers in PubMed, 88 citations in OpenAlex.

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  20. Small-molecule control of CAR T cells.Nature reviews. Chemistry · 2025
    Review

15 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

12 authors at 2 institutions in 1 country.

Alfonso R Sánchez-Paulete *Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-7475-1913
Jaime Mateus-Tique *Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-6591-379X
Gurkan MollaogluPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-0679-7463
Sebastian R NielsenPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-8449-476X
Adam MarksPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-9311-9929
Ashwitha LakshmiDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-5525-3409
Jalal A KhanPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-1965-4069
C Matthias WilkPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0001-5429-7143
Luisanna PiaPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-4358-6721
Alessia BaccariniPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0003-4727-0668
Miriam MeradPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-4481-7827
Brian D BrownPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.ORCID 0000-0002-3670-8778
Icahn School of Medicine at Mount Sinai · USTisch Hospital · US

Funding

Investigating Macrophage Molecular and Functional Diversity in Tumor ImmunityR01CA254104 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BROWN, BRIAN D, MERAD, MIRIAM · 2021 to 2025
$3.4M
Dissecting the pathways driving progenitor to pro-tumor macrophage programmingR01CA257195 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Brian D Brown, MIRIAM MERAD · 2021 to 2026
$3.3M
NCI NIH HHS R01 CA254104NCI NIH HHS R01 CA257195
6 · The paper itself

Abstract

Tumor-associated macrophages (TAM) are one of the most abundant cell types in many solid tumors and typically exert protumor effects. This has led to an interest in macrophage-depleting agents for cancer therapy, but approaches developed to date have had limited success in clinical trials. Here, we report the development of a strategy for TAM depletion in mouse solid tumor models using chimeric antigen receptor (CAR) T cells targeting the macrophage marker F4/80 (F4.CAR-T). F4.CAR-T cells effectively killed macrophages in vitro and in vivo without toxicity. When injected into mice bearing orthotopic lung tumors, F4.CAR-T cells infiltrated tumor lesions and delayed tumor growth comparably with PD-1 blockade, and significantly extended mouse survival. Antitumor effects were mediated by F4.CAR-T-produced IFNγ, which promoted upregulation of MHC molecules on cancer cells and tumor-infiltrating myeloid cells. Notably, F4.CAR-T promoted expansion of endogenous CD8 T cells specific for tumor-associated antigen and led to immune editing of highly antigenic tumor cell clones. Antitumor impact was also observed in mouse models of ovarian and pancreatic cancer. These studies provide proof of principle to support CAR T-cell targeting of TAMs as a means to enhance antitumor immunity.

Indexed as

Receptors, Chimeric AntigenT-LymphocytesAnimalsAntigens, NeoplasmCell Line, TumorDisease Models, AnimalDisease ProgressionImmunotherapy, AdoptiveMacrophagesMiceXenograft Model Antitumor AssaysAntigens, NeoplasmReceptors, Chimeric Antigen

Identifiers

PMID36095236
PMCPMC10704925
OpenAlexW4295309587

What OpenQuestion holds

Textmetadata
LicenceTDM
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.