Evidence map›Paper›PMID 41715067›Full record

ArticleBMC biotechnology2026

Cultivation strategy optimisation for NK-92 cell line expansion in static conditions.

Valentin von Werz, Aleksander Szarzynski, Gregor Mattert, Sara Zigon-Branc, Werner Dammermann, Oliver Spadiut

Abstract read
In one paragraph

Article in BMC biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. A novel cultivation strategy to recover NK cell cytotoxicity.Frontiers in bioengineering and biotechnology · 2026
    Article
  4. Article
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.

Valentin von WerzResearch Area Biochemical Engineering, Institute of Chemical, Environmental and Bioscience Engineering, TU Wien, Vienna, 1060, Austria.
Aleksander SzarzynskiResearch Area Biochemical Engineering, Institute of Chemical, Environmental and Bioscience Engineering, TU Wien, Vienna, 1060, Austria.
Gregor MattertCenter for Translational Medicine Germany, University Hospital Brandenburg, Brandenburg Medical School Theodor Fontane, 14770, Brandenburg an der Havel, Germany.
Sara Zigon-BrancResearch Area Biochemical Engineering, Institute of Chemical, Environmental and Bioscience Engineering, TU Wien, Vienna, 1060, Austria.
Werner DammermannCenter for Translational Medicine Germany, University Hospital Brandenburg, Brandenburg Medical School Theodor Fontane, 14770, Brandenburg an der Havel, Germany.
Oliver SpadiutResearch Area Biochemical Engineering, Institute of Chemical, Environmental and Bioscience Engineering, TU Wien, Vienna, 1060, Austria. oliver.spadiut@tuwien.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural killer cells play a critical role in innate immunity by targeting and eliminating cancerous and infected cells. The cell line NK-92, currently used in several clinical trials, has shown great potential in cancer immunotherapy due to strong cytotoxic capabilities and suitability as an off-the-shelf therapy. However, effective clinical application of NK-92 therapies requires optimised cell culture conditions, including cultivation medium composition and expansion methods. This study aimed at identifying optimal cultivation medium formulations and intensifying NK-92 cell expansion by systematically evaluating critical quality attributes and key performance indicators.

resultsWe screened various cultivation media formulations, including alpha minimum essential medium, Roswell Park Memorial Institute medium, and stem cell growth medium, supplemented with either human serum, fetal bovine serum, chemically defined serum replacement, and a combination of fetal bovine serum and horse serum. Cells cultivated in alpha minimum essential medium supplemented with human serum significantly outperformed the other formulations, achieving the highest growth rate, maximum viable cell count, and superior cytotoxicity at high cost-efficiency. Media containing chemically defined serum replacement showed reduced cell proliferation despite high cytotoxicity per cell, indicating a complex balance between cell quantity and functionality. Following cultivation medium selection, cultivation strategies including batch, fed-batch, and repetitive batch were compared. The repetitive batch method, where cultivation medium is replenished repeatedly throughout the cultivation, demonstrated superior expansion capability, long-term cell viability, significantly improved cytotoxicity, although associated with higher medium consumption and thus costs.

conclusionsThis study identified alpha minimum essential medium supplemented with human serum in repetitive batch cultivation as the optimal approach for NK-92 cell expansion. This combination enhances cell growth, viability, and cytotoxicity, meeting essential clinical quality attributes while maintaining cost-effectiveness. These findings provide valuable guidance and should act as a baseline for consistent, scalable, and commercially viable production of NK cell-based cancer therapies.

Indexed as

Cell Culture TechniquesCulture MediaKiller Cells, NaturalAnimalsCell LineCell ProliferationCell SurvivalHumansCulture MediaBatchCultivation medium optimisationFed-batchNatural killer cellsNK-92 cellsProcess intensificationProcess modeRepetitive batch

Identifiers

PMID41715067
PMCPMC12997954

What Socratic holds

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LicenceCC BY
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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.