Evidence map›Paper›PMID 40476558›Full record

ReviewMolecular medicine reports2025

IPSC‑derived NK cells for immunotherapy and therapeutic perspective (Review).

Xiyao Wei, Chen Su, Yueyang Liu, Ningbo Wei, Kexin Xiang, Qijun Qian, Zenghui Xu

Abstract readReview
In one paragraph

Review in Molecular medicine reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. NK cells in HPV-related tumorigenesis: mechanisms and clinical applications.Frontiers in cellular and infection microbiology · 2025
    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

7 authors.

Xiyao WeiShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Chen SuShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Yueyang LiuShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Ningbo WeiShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Kexin XiangShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Qijun QianShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.
Zenghui XuShanghai Cell Therapy Group Co., Ltd., Shanghai 201805, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cell‑based immunotherapy has emerged as a transformative approach for cancer treatment However, its widespread clinical application faces several challenges, such as donor variability, limited scalability and functional heterogeneity of primary NK cells. Additionally, issues including

Indexed as

ImmunotherapyInduced Pluripotent Stem CellsKiller Cells, NaturalNeoplasmsAnimalsCell DifferentiationGene EditingHumansImmunotherapy, Adoptiveimmunotherapyinduced pluripotent stem cell derived natural killer cellsnatural killer cellsoff‑the‑shelfsolid tumors

Identifiers

PMID40476558
PMCPMC12174902

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.