Evidence map›Paper›PMID 38564778›Full record

ArticleBlood advances2024

CD70-specific CAR NK cells expressing IL-15 for the treatment of CD19-negative B-cell malignancy.

Shanshan Guo, Wen Lei, Xueli Jin, Hui Liu, James Q Wang, Wenhai Deng, Wenbin Qian

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
10.5field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 37 citations in OpenAlex.

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  15. Targets for CAR Therapy in Multiple Myeloma.International journal of molecular sciences · 2025
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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

7 authors at 3 institutions in 1 country.

Shanshan GuoDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.
Wen LeiDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.
Xueli JinDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.ORCID 0000-0001-5618-920X
Hui LiuDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.ORCID 0000-0003-1452-5062
James Q WangDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.
Wenhai DengOujiang Laboratory (Zhejiang Lab for Regenerative Medicine, Vision, and Brain Health), School of Laboratory Medicine and Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, China.ORCID 0000-0003-3270-5980
Wenbin QianDepartment of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Haining, China.ORCID 0000-0002-9817-6674
Ministry of Education of the People's Republic of China · CNSecond Affiliated Hospital of Zhejiang University · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractChimeric antigen receptor (CAR) natural killer (NK) cells can eliminate tumors not only through the ability of the CAR molecule to recognize antigen-expressed cancer cells but also through NK-cell receptors themselves. This overcomes some of the limitations of CAR T cells, paving the way for CAR NK cells for safer and more effective off-the-shelf cellular therapy. In this study, CD70-specific (a pan-target of lymphoma) fourth-generation CAR with 4-1BB costimulatory domain and interleukin-15 (IL-15) was constructed and transduced into cord blood-derived NK cells by Baboon envelope pseudotyped lentiviral vector. CD70-CAR NK cells displayed superior cytotoxic activity in vitro and in vivo against CD19-negative B-cell lymphoma when compared with nontransduced NK cells and CD19-specific CAR NK cells. Importantly, mice that received 2 doses of CD70-CAR NK cells showed effective eradication of tumors, accompanied by increased concentration of plasma IL-15 and enhanced CAR NK cell proliferation and persistence. Our study suggests that repetitive administration-based CAR NK-cell therapy has clinical advantage compared with a single dose of CAR NK cells for the treatment of B-cell lymphoma.

Indexed as

Antigens, CD19CD27 LigandImmunotherapy, AdoptiveInterleukin-15Killer Cells, NaturalLymphoma, B-CellReceptors, Chimeric AntigenAnimalsCell Line, TumorCytotoxicity, ImmunologicHumansMiceXenograft Model Antitumor AssaysAntigens, CD19CD27 LigandCD70 protein, humanInterleukin-15Receptors, Chimeric Antigen

Identifiers

PMID38564778
PMCPMC11157212
OpenAlexW4393577391

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.