Evidence map›Paper›PMID 30634595›Full record

ArticleCancers2019

Functional Assessment for Clinical Use of Serum-Free Adapted NK-92 Cells.

Michael Chrobok, Carin I M Dahlberg, Ece Canan Sayitoglu, Vladimir Beljanski, Hareth Nahi, Mari Gilljam, Birgitta Stellan, Tolga Sutlu, Adil Doganay Duru, Evren Alici

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. A novel cultivation strategy to recover NK cell cytotoxicity.Frontiers in bioengineering and biotechnology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. TCR-NK Cells: A Novel Source for Adoptive Immunotherapy of CancerTurkish journal of haematology : official journal of Turkish Society of Haematology · 2023
    Review
  8. Review
  9. Article
  10. Advances in NK cell production.Cellular & molecular immunology · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. 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

10 authors at 4 institutions in 3 countries.

Michael ChrobokCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. Michael.Chrobok@ki.se.
Carin I M DahlbergCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. Carin.Dahlberg@ki.se.
Ece Canan SayitogluNSU Cell Therapy Institute, Nova Southeastern University, Fort Lauderdale, FL 33314, USA. esayitoglu@nova.edu.
Vladimir BeljanskiNSU Cell Therapy Institute, Nova Southeastern University, Fort Lauderdale, FL 33314, USA. vbeljanski@nova.edu.
Hareth NahiCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. Hareth.Nahi@ki.se.ORCID 0000-0003-4711-5094
Mari GilljamCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. Mari.Gilljam@ki.se.
Birgitta StellanCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. birgittastellan@gmail.com.
Tolga SutluNanotechnology Research and Application Center, Sabanci University, 34956 Istanbul, Turkey. tolgasutlu@sabanciuniv.edu.ORCID 0000-0002-7813-8734
Adil Doganay DuruNSU Cell Therapy Institute, Nova Southeastern University, Fort Lauderdale, FL 33314, USA. adil.duru@nova.edu.
Evren AliciCenter for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, 141 83 Stockholm, Sweden. evren.alici@ki.se.
Karolinska Institutet · SENova Southeastern University · USKarolinska University Hospital · SESabancı Üniversitesi · TR

Funding

Cancerföreningen i Stockholm 141022
6 · The paper itself

Abstract

Natural killer (NK) cells stand out as promising candidates for cellular immunotherapy due to their capacity to kill malignant cells. However, the therapeutic use of NK cells is often dependent on cell expansion and activation with considerable amounts of serum and exogenous cytokines. We aimed to develop an expansion protocol for NK-92 cells in an effort to generate a cost-efficient, xeno-free, clinical grade manufactured master cell line for therapeutic applications. By making functional assays with NK-92 cells cultured under serum-free conditions (NK-92

Indexed as

immunotherapyNK-92NK cellserum-free

Identifiers

PMID30634595
PMCPMC6356567
OpenAlexW2908759880

What Socratic 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 Socratic graph.