Evidence map›Paper›PMID 38140726›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2024

Dexamethasone potentiates chimeric antigen receptor T cell persistence and function by enhancing IL-7Rα expression.

Ashlie M Munoz, Ryan Urak, Ellie Taus, Hui-Ju Hsieh, Dennis Awuah, Vibhuti Vyas, Laura Lim, Katherine Jin, Shu-Hong Lin, Saul J Priceman and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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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

14 authors at 3 institutions in 1 country.

Ashlie M MunozDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Ryan UrakDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Ellie TausDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Hui-Ju HsiehDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Dennis AwuahDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Vibhuti VyasDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Laura LimDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Katherine JinDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Shu-Hong LinDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, 20892, USA.
Saul J PricemanDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Mary C ClarkDepartment of Clinical Translational Project Development, City of Hope, Duarte, CA 91010, USA.
Lior GoldbergDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Stephen J FormanDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA.
Xiuli WangDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA 91010, USA. Electronic address: xiuwang@coh.org.
City of Hope · USCity Of Hope National Medical Center · USNational Cancer Institute · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
Transplant for Lymphoma:Therapy-Related LeukemiaP50CA107399 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI KWAK, LARRY W · 2004 to 2022
$35.5M
NCI NIH HHS P30 CA033572NCI NIH HHS P50 CA107399
6 · The paper itself

Abstract

Dexamethasone (dex) is a glucocorticoid that is a mainstay for the treatment of inflammatory pathologies, including immunotherapy-associated toxicities, yet the specific impact of dex on the activity of CAR T cells is not fully understood. We assessed whether dex treatment given ex vivo or as an adjuvant in vivo with CAR T cells impacted the phenotype or function of CAR T cells. We demonstrated that CAR T cell expansion and function were not inhibited by dex. We confirmed this observation using multiple CAR constructs and tumor models, suggesting that this is a general phenomenon. Moreover, we determined that dex upregulated interleukin-7 receptor α on CAR T cells and increased the expression of genes involved in activation, migration, and persistence when supplemented ex vivo. Direct delivery of dex and IL-7 into tumor-bearing mice resulted in increased persistence of adoptively transferred CAR T cells and complete tumor regression. Overall, our studies provide insight into the use of dex to enhance CAR T cell therapy and represent potential novel strategies for augmenting CAR T cell function during production as well as following infusion into patients.

Indexed as

NeoplasmsReceptors, Chimeric AntigenReceptors, Interleukin-7AnimalsDexamethasoneHumansImmunotherapy, AdoptiveMiceReceptors, Antigen, T-CellT-LymphocytesDexamethasoneinterleukin-7 receptor, alpha chainReceptors, Antigen, T-CellReceptors, Chimeric AntigenReceptors, Interleukin-7CARCAR T cellschimeric antigen receptordexamethasoneglucocorticoidIL-7Rα

Identifiers

PMID38140726
PMCPMC10861975
OpenAlexW4390115637

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.