Evidence map›Paper›PMID 38070118›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

How to Test Human CAR T Cells in Solid Tumors, the Next Frontier of CAR T Cell Therapy.

Russell W Cochrane, Andrew Fiorentino, Eva Allen, Rob A Robino, Jaime Quiroga, Leonardo M R Ferreira

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. 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
1.4field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Generation of Human Chimeric Antigen Receptor Regulatory T Cells.Journal of visualized experiments : JoVE · 2025
    Article
  3. Article
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

6 authors at 2 institutions in 1 country.

Russell W CochraneDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Andrew FiorentinoDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Eva AllenDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Rob A RobinoDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Jaime QuirogaDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA.
Leonardo M R FerreiraDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, USA. ferreirl@musc.edu.
Medical University of South Carolina · USMUSC Hollings Cancer Center · US

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Jian Ouyang · 2009 to 2026
$42.7M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Renewal of the Human Islet Research Enhancement Center (HIREC) for the Type-1-Diabetes-Focused Human Islet Research Network (HIRN).U24DK104162 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI John S. Kaddis, Joyce Carol Niland · 2019 to 2026
$12.3M
Cellular, Biochemical and Molecular Sciences Training Program: Developing the skills and expertise needed for a changing biomedical landscapeT32GM132055 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Amy D Bradshaw, John P O'Bryan · 2019 to 2026
$3.9M
NCATS NIH HHS UL1 TR001450NCI NIH HHS P30 CA138313NIDDK NIH HHS U24 DK104162NIGMS NIH HHS T32 GM132055
6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cell therapy has proven to be a successful treatment option for leukemias and lymphomas. These encouraging outcomes underscore the potential of adoptive cell therapy for other oncology applications, namely, solid tumors. However, CAR T cells are yet to succeed in treating solid tumors. Unlike liquid tumors, solid tumors create a hostile tumor microenvironment (TME). CAR T cells must traffic to the TME, survive, and retain their function to eradicate the tumor. Nevertheless, there is no universal preclinical model to systematically test candidate CARs and CAR targets for their capacity to infiltrate and eliminate human solid tumors in vivo. Here, we provide a detailed protocol to evaluate human CAR CD4

Indexed as

NeoplasmsReceptors, Chimeric AntigenAnimalsHumansImmunotherapy, AdoptiveMiceT-LymphocytesTumor MicroenvironmentReceptors, Chimeric AntigenCancerChimeric antigen receptorInfiltrationMicroenvironmentModelSolid tumorSynthetic immunologyT cellTrafficking

Identifiers

PMID38070118
PMCPMC11649538
OpenAlexW4389508000

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.