Evidence map›Paper›PMID 25309538›Full record

ReviewFrontiers in immunology2014

Natural killer cells for cancer immunotherapy: pluripotent stem cells-derived NK cells as an immunotherapeutic perspective.

Cristina Eguizabal, Olatz Zenarruzabeitia, Jorge Monge, Silvia Santos, Miguel Angel Vesga, Natalia Maruri, Arantza Arrieta, Marta Riñón, Estibaliz Tamayo-Orbegozo, Laura Amo and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

56 citing papers in PubMed, 95 citations in OpenAlex.

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  8. Advanced T and Natural Killer Cell Therapy for Glioblastoma.Journal of Korean Neurosurgical Society · 2023
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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

12 authors at 3 institutions in 1 country.

Cristina EguizabalBasque Center for Transfusion and Human Tissues , Galdakao , Spain.
Olatz ZenarruzabeitiaImmunopathology Group, BioCruces Health Research Institute , Barakaldo , Spain.
Jorge MongeBasque Center for Transfusion and Human Tissues , Galdakao , Spain.
Silvia SantosBasque Center for Transfusion and Human Tissues , Galdakao , Spain.
Miguel Angel VesgaBasque Center for Transfusion and Human Tissues , Galdakao , Spain.
Natalia MaruriRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Arantza ArrietaRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Marta RiñónRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Estibaliz Tamayo-OrbegozoRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Laura AmoRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Susana LarruceaRegulation of the Immune System Group, BioCruces Health Research Institute , Barakaldo , Spain.
Francisco BorregoImmunopathology Group, BioCruces Health Research Institute , Barakaldo , Spain ; Ikerbasque, Basque Foundation for Science , Bilbao , Spain.
BioCruces Health research Institute · ESBasque Center for Materials, Applications and Nanostructures · ESIkerbasque · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells play an essential role in the fight against tumor development. Over the last years, the progress made in the NK-cell biology field and in deciphering how NK-cell function is regulated, is driving efforts to utilize NK-cell-based immunotherapy as a promising approach for the treatment of malignant diseases. Therapies involving NK cells may be accomplished by activating and expanding endogenous NK cells by means of cytokine treatment or by transferring exogenous cells by adoptive cell therapy and/or by hematopoietic stem cell transplantation. NK cells that are suitable for adoptive cell therapy can be derived from different sources, including ex vivo expansion of autologous NK cells, unstimulated or expanded allogeneic NK cells from peripheral blood, derived from CD34+ hematopoietic progenitors from peripheral blood and umbilical cord blood, and NK-cell lines. Besides, genetically modified NK cells expressing chimeric antigen receptors or cytokines genes may also have a relevant future as therapeutic tools. Recently, it has been described the derivation of large numbers of functional and mature NK cells from pluripotent stem cells, both embryonic stem cells and induced pluripotent stem cells, which adds another tool to the expanding NK-cell-based cancer immunotherapy arsenal.

Indexed as

adoptive cell therapycancer immunotherapyembryonic stem cellshematopoietic stem cell transplantationinduced pluripotent stem cellsNK cellspluripotent stem cells

Identifiers

PMID25309538
PMCPMC4164009
OpenAlexW2069504907

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.