Evidence map›Paper›PMID 41915242›Full record

ArticleCancer immunology, immunotherapy : CII2026

An innovative treatment for lung cancer using gene-engineered human-induced pluripotent stem cell-derived natural killer cells.

Yuka Sato, Kumiko Goto, Shigehiro Yagishita, Kotoko Miyata, Noriko Uesugi, Yu-Suke Torisawa, Yoichi Naritomi, Ryuta Takahashi, Rumiko Sho, Yuriko Takeno and 7 more

Abstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Yuka SatoKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Kumiko GotoKobe Research Institute, HEALIOS K.K, Kobe, Japan. k.goto@healios.jp.
Shigehiro YagishitaDivision of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
Kotoko MiyataKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Noriko UesugiKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Yu-Suke TorisawaKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Yoichi NaritomiKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Ryuta TakahashiKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Rumiko ShoKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Yuriko TakenoKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Kenji KurachiKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Masashi YamadaKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Yasuyuki HigashiKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Hironobu KimuraKobe Research Institute, HEALIOS K.K, Kobe, Japan.
Akinobu HamadaDivision of Molecular Pharmacology, National Cancer Center Research Institute, Tokyo, Japan.
Fusako NishigakiKobe Research Institute, HEALIOS K.K, Kobe, Japan. nishigaki_y2t9@hh-hikari.com.
Kouichi TamuraKobe Research Institute, HEALIOS K.K, Kobe, Japan.

Funding

Japan Agency for Medical Research and Development 17pc0101011h0001
6 · The paper itself

Abstract

Various therapeutic approaches have been developed for lung cancer, including chemotherapy, radiation therapy, and immune checkpoint inhibitors. However, these approaches, including chimeric antigen receptor (CAR)-T cell therapy, have shown limited efficacy against solid tumors, especially in advanced disease.To enhance the therapeutic effect, we focused on the multiple effects of a new modality of cell therapy and created engineered natural killer (eNK) cells, which are gene-engineered induced pluripotent stem cell (iPSC)-derived NK cells armed with CC motif ligand 19 (CCL19), CC chemokine receptor type 2B (CCR2B), high-affinity cluster of differentiation 16 (CD16), interleukin (IL)-15, and natural killer group 2, member D (NKG2D)-DNAX-activating protein 10 (DAP10) complex. In vitro studies showed that eNK cells exhibit significant long-lasting cytotoxicity and antibody-dependent cell-mediated cytotoxicity (ADCC) against human lung cancer cell lines. In vivo, eNK cells achieved near-complete tumor regression in orthotopic and subcutaneous cell line-derived xenograft (CDX) models. In contrast, in patient-derived xenograft (PDX) models, eNK cells demonstrated modest tumor growth inhibition (28% reduction) as monotherapy and significantly enhanced efficacy (53% inhibition) in combination with cetuximab via antibody-dependent cellular cytotoxicity. In treated PDX tumors, human CD45-positive cells were detected within the tumor parenchyma, supporting intratumoral presence of administered human cells.These findings support the potential contribution of the five-gene modifications in enhancing tumor homing, persistence, and cytotoxicity in solid tumor treatment. This study underscores the potential of eNK cells as a novel, "off-the-shelf" allogeneic therapy for refractory solid tumors, including lung cancer.

Indexed as

Immunotherapy, AdoptiveInduced Pluripotent Stem CellsKiller Cells, NaturalLung NeoplasmsAnimalsCell Line, TumorGenetic EngineeringHumansMiceXenograft Model Antitumor AssaysCell therapyGenetic engineeringiPSC (induced pluripotent stem cell)Lung cancerNK (natural killer) cellsPDX (Patient-derived xenograft)

Identifiers

PMID41915242
PMCPMC13038767

What OpenQuestion holds

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Registered trials

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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.