Evidence map›Paper›PMID 37205115›Full record

ReviewFrontiers in immunology2023

Advancements in CAR-NK therapy: lessons to be learned from CAR-T therapy.

Marisa K Kilgour, Donald J Bastin, Seung-Hwan Lee, Michele Ardolino, Scott McComb, Alissa Visram

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

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  13. From lab to lifesaver: the rise of CAR T-cell therapy in oncology.Journal of the Egyptian National Cancer Institute · 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

6 authors.

Marisa K KilgourCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Donald J BastinDepartment of Medicine, University of Ottawa, Ottawa, Canada.
Seung-Hwan LeeDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada.
Michele ArdolinoCancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Canada.
Scott McCombDepartment of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Canada.
Alissa VisramDepartment of Medicine, University of Ottawa, Ottawa Hospital Research Institute, Ottawa, Canada.

Funding

CIHR
6 · The paper itself

Abstract

Advancements in chimeric antigen receptor engineered T-cell (CAR-T) therapy have revolutionized treatment for several cancer types over the past decade. Despite this success, obstacles including the high price tag, manufacturing complexity, and treatment-associated toxicities have limited the broad application of this therapy. Chimeric antigen receptor engineered natural killer cell (CAR-NK) therapy offers a potential opportunity for a simpler and more affordable "off-the-shelf" treatment, likely with fewer toxicities. Unlike CAR-T, CAR-NK therapies are still in early development, with few clinical trials yet reported. Given the challenges experienced through the development of CAR-T therapies, this review explores what lessons we can apply to build better CAR-NK therapies. In particular, we explore the importance of optimizing the immunochemical properties of the CAR construct, understanding factors leading to cell product persistence, enhancing trafficking of transferred cells to the tumor, ensuring the metabolic fitness of the transferred product, and strategies to avoid tumor escape through antigen loss. We also review trogocytosis, an important emerging challenge that likely equally applies to CAR-T and CAR-NK cells. Finally, we discuss how these limitations are already being addressed in CAR-NK therapies, and what future directions may be possible.

Indexed as

NeoplasmsReceptors, Chimeric AntigenHumansImmunotherapy, AdoptiveKiller Cells, NaturalT-LymphocytesReceptors, Chimeric Antigencancerchimeric antigen receptorimmunotherapynatural kill cellT celltrogocytosis

Identifiers

PMID37205115
PMCPMC10187144

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.