Evidence map›Paper›PMID 41131610›Full record

ReviewJournal of translational medicine2025

CAR-T and CAR-NK cell therapies in AML: breaking barriers and charting the future.

Huichao Wu, Fatemeh Sadat Shafiei, Zahra Taghinejad, Mohsen Maleknia, Hanieh Noormohamadi, Atieh Raoufi, Sina Nouri, Nazli Servatian, Hamed Soleimani Samarkhazan

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
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  5. Article
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  9. Oncology research · 2026
    Review
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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

9 authors.

Huichao WuDept Emergency, First Peoples Hosp Jiashan, Jiashan, 314100, Zhejiang, People's Republic of China. 525865994@qq.com.
Fatemeh Sadat ShafieiDepartment of Medical Laboratory Sciences, School of Paramedical Sciences, Zanjan University of Medical Sciences, Zanjan, Iran.ORCID 0009-0003-7769-8320
Zahra TaghinejadDepartment of Hematology and Blood Banking, School of Medical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.ORCID 0000-0001-7373-6092
Mohsen MalekniaMasih Daneshvari Hospital, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), WHO Collaborating Centre (WHOCC), Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-4559-6525
Hanieh NoormohamadiDepartment of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-9755-2850
Atieh RaoufiStudent Research Committee, Department of Immunology, School of Medicine, Zanjan University of Medical Science, Zanjan, Iran.ORCID 0000-0002-1029-751X
Sina NouriDepartment of Immunology, Faculty of Medicine, Tabriz University of Medical Science, Tabriz, Iran.ORCID 0000-0003-4863-2595
Nazli ServatianCord Blood Bank Laboratory Department, Royan Stem Cell Technology Company, Tehran, Iran.ORCID 0000-0002-7120-9173
Hamed Soleimani SamarkhazanStudent Research Committee, Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Hamed.soleimani.s@gmail.com.ORCID 0000-0003-1045-7613

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML), characterized by aggressive relapse and dismal survival, remains a formidable challenge despite conventional therapies. Chimeric antigen receptor (CAR)-engineered T and natural killer (NK) cells have emerged as groundbreaking immunotherapies, offering targeted eradication of leukemic stem cells (LSCs) and resistant blasts. CAR-T cells, leveraging antigens like CD123 and CD33, demonstrate early clinical success, with complete remission rates up to 66% in refractory/relapsed (R/R) AML. CAR-NK cells complement this approach through inherent tumor surveillance, reduced toxicity, and "off-the-shelf" feasibility. However, barriers such as antigen escape, heterogeneous immunosuppressive microenvironments (including intratumoral microbiota variations), and on-target/off-tumor toxicity persist, limiting durable responses. Innovations in dual-targeting CARs, cytokine-armored constructs, and CRISPR-edited universal cells aim to overcome these hurdles. Emerging strategies integrating checkpoint inhibitors, metabolic modulators, and AI-driven antigen selection promise to enhance efficacy and safety. This review synthesizes the evolving landscape of CAR-T/NK therapies, critically analyzing preclinical breakthroughs, clinical trial outcomes, and persisting challenges. By addressing manufacturing scalability, cost barriers, and long-term safety, cellular immunotherapy holds transformative potential to redefine AML management. As the field advances, interdisciplinary collaboration and biomarker-guided personalization will be pivotal in translating laboratory innovations into life-saving therapies for AML patients.

Indexed as

Immunotherapy, AdoptiveKiller Cells, NaturalLeukemia, Myeloid, AcuteReceptors, Chimeric AntigenAnimalsHumansReceptors, Chimeric AntigenAcute myeloid leukemiaCAR-NK cell therapyCAR-T-cell therapyImmunotherapyTumor Microenvironment

Identifiers

PMID41131610
PMCPMC12548124

What Socratic 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 Socratic graph.