Evidence map›Paper›PMID 38414243›Full record

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

Stem cell-derived CAR T cells show greater persistence, trafficking, and viral control compared to ex vivo transduced CAR T cells.

Mayra A Carrillo, Anjie Zhen, Wenli Mu, Valerie Rezek, Heather Martin, Christopher W Peterson, Hans-Peter Kiem, Scott G Kitchen

Open access · greenAbstract 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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
6.5field-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

17 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Beyond autologousMolecular therapy. Oncology · 2026
    Review
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  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Terminally exhausted CD8Frontiers in immunology · 2025
    Review
  11. Review
  12. Review
  13. Review
  14. Humanized Mouse Models of Bacterial Infections.Antibiotics (Basel, Switzerland) · 2024
    Review
  15. Review
  16. Article
  17. 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

8 authors at 3 institutions in 2 countries.

Mayra A CarrilloDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Anjie ZhenDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Wenli MuDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Valerie RezekDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Heather MartinDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA.
Christopher W PetersonStem Cell and Gene Therapy Program, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Medicine, University of Washington, Seattle, WA, USA.
Hans-Peter KiemStem Cell and Gene Therapy Program, Fred Hutchinson Cancer Research Center, Seattle, WA, USA; Department of Medicine, University of Washington, Seattle, WA, USA.
Scott G KitchenDepartment of Medicine, Division of Hematology and Oncology, and UCLA AIDS Institute, University of California, Los Angeles (UCLA), Los Angeles, CA, USA; Broad Stem Cell Research Center, Jonsson Comprehensive Cancer Center, and Molecular Biology Institute, UCLA, Los Angeles, CA, USA. Electronic address: skitchen@ucla.edu.
APLA Health · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAUniversity of California, Los Angeles · US

Funding

Washington National Primate Research CenterP51OD010425 · OD · UNIVERSITY OF WASHINGTON · PI Mari Ostendorf · 2012 to 2026
$201.8M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ZACK, JEROME A. · 1991 to 2018
$39.9M
WaNPRC Macaca nemestrina SPF Breeding ColonyU42OD011123 · OD · UNIVERSITY OF WASHINGTON · PI Richard Grant · 2012 to 2026
$34.4M
Cell and Gene Therapy for HIV CureUM1AI126623 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI JEROME, KEITH R, KIEM, HANS-PETER · 2016 to 2020
$24.2M
UCLA-CDU CFARP30AI152501 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SCOTT G KITCHEN · 2022 to 2026
$15.6M
Primate CoreU19HL156247 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CANNON, PAULA M, KIEM, HANS-PETER · 2020 to 2024
$14.6M
Viral Immunology CoreU19AI149504 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHEN, IRVIN S.Y., KITCHEN, SCOTT G · 2020 to 2024
$14.3M
UPLIFT: UCLA Postdocs' Longitudinal Investment in Faculty TrainingK12GM106996 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CAREY, MICHAEL F, VILLANUEVA, CLAUDIO J · 2016 to 2025
$7.1M
In Vivo Gene Editing of B cells with NICE-AAV VectorsR01AI167004 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Christopher W Peterson · 2022 to 2026
$3.7M
Developing Durable, Env-Boosted CAR T Cells for HIV CureR01AI170214 · NIAID · FRED HUTCHINSON CANCER CENTER · PI Christopher W Peterson · 2023 to 2026
$3.4M
Define the effects and mechanism of THC and CBD on IFN-I mediated inflammation and immune dysfunction during HIV infectionR01DA052841 · NIDA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G, ZHEN, ANJIE · 2020 to 2024
$1.9M
Role of persistent type I IFN signaling in immune suppression and tumorigenesis during chronic HIV infectionR01CA239261 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KITCHEN, SCOTT G · 2019 to 2023
$1.8M
NCI NIH HHS R01 CA239261NHLBI NIH HHS U19 HL156247NIAID NIH HHS P30 AI028697NIAID NIH HHS P30 AI152501NIAID NIH HHS R01 AI167004NIAID NIH HHS R01 AI170214NIAID NIH HHS R21 AI140866NIAID NIH HHS R21 AI172582NIAID NIH HHS U19 AI149504NIAID NIH HHS UM1 AI126623NIDA NIH HHS R01 DA052841NIGMS NIH HHS K12 GM106996NIH HHS P51 OD010425NIH HHS U42 OD011123
6 · The paper itself

Abstract

Adoptive cell therapy (ACT) using T cells expressing chimeric antigen receptors (CARs) is an area of intense investigation in the treatment of malignancies and chronic viral infections. One of the limitations of ACT-based CAR therapy is the lack of in vivo persistence and maintenance of optimal cell function. Therefore, alternative strategies that increase the function and maintenance of CAR-expressing T cells are needed. In our studies using the humanized bone marrow/liver/thymus (BLT) mouse model and nonhuman primate (NHP) model of HIV infection, we evaluated two CAR-based gene therapy approaches. In the ACT approach, we used cytokine enhancement and preconditioning to generate greater persistence of anti-HIV CAR

Indexed as

HIV-1HIV InfectionsReceptors, Chimeric AntigenAnimalsHematopoietic Stem CellsImmunotherapy, AdoptiveMiceT-LymphocytesReceptors, Chimeric Antigenadoptive cell therapyCAR T cellsHIVhumanized mouse modelnonhuman primate modelstem cell gene therapy

Identifiers

PMID38414243
PMCPMC11163220
OpenAlexW4392202195

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.