Evidence map›Paper›PMID 39496674›Full record

ArticleScientific reports2024

Automated and closed clinical-grade manufacturing protocol produces potent NK cells against neuroblastoma cells and AML blasts.

Farhana Jahan, Leena Penna, Annu Luostarinen, Laurens Veltman, Heidi Hongisto, Kaarina Lähteenmäki, Sabine Müller, Seppo Ylä-Herttuala, Matti Korhonen, Kim Vettenranta and 3 more

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. A novel cultivation strategy to recover NK cell cytotoxicity.Frontiers in bioengineering and biotechnology · 2026
    Article
  9. Challenges and opportunities of human iPSC-derived NK as "Off-the-shelf" cellular therapies.Journal of experimental & clinical cancer research : CR · 2025
    Review
  10. Review
  11. Review
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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

13 authors.

Farhana JahanFinnish Red Cross Blood Service, Research and Development, Helsinki, Finland.
Leena PennaFinnish Red Cross Blood Service, Advanced Cell Therapy Centre, Vantaa, Finland.
Annu LuostarinenFinnish Red Cross Blood Service, Advanced Cell Therapy Centre, Vantaa, Finland.
Laurens VeltmanFinnish Red Cross Blood Service, Research and Development, Helsinki, Finland.
Heidi HongistoFinnish Red Cross Blood Service, Advanced Cell Therapy Centre, Vantaa, Finland.
Kaarina LähteenmäkiFinnish Red Cross Blood Service, Quality Management, Vantaa, Finland.
Sabine MüllerMiltenyi Biotec B.V. & Co. KG, R&D Reagents, Bergisch Gladbach, Germany.
Seppo Ylä-HerttualaTranslational Cancer Medicine Research Program, University of Eastern Finland, Kuopio, Finland.
Matti KorhonenFinnish Red Cross Blood Service, Research and Development, Helsinki, Finland.
Kim VettenrantaFinnish Red Cross Blood Service, Research and Development, Helsinki, Finland.
Anita LaitinenFinnish Red Cross Blood Service, Advanced Cell Therapy Centre, Vantaa, Finland.
Urpu SalmenniemiStem Cell Transplantation Unit, Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland.
Erja KerkeläFinnish Red Cross Blood Service, Advanced Cell Therapy Centre, Vantaa, Finland. erja.kerkela@bloodservice.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are a promising allogeneic immunotherapy option due to their natural ability to kill tumor cells, and due to their apparent safety. This study describes the development of a GMP-compliant manufacturing protocol for the local production of functionally potent NK cells tailored for high-risk acute myeloid leukemia (AML) and neuroblastoma (NBL) patients. Moreover, the quality control strategy and considerations for product batch specifications in early clinical development are described. The protocol is based on the CliniMACS Prodigy platform and Natural Killer Cell Transduction (NKCT) (Miltenyi Biotec). NK cells are isolated from leukapheresis through CD3 depletion and CD56 enrichment, followed by a 12-hour activation with IL-2 and IL-15 cytokines. Three CliniMACS Prodigy processes demonstrated the feasibility and consistency of the modified NKCT process. A three-step process without expansion, however, compromised the NK cell yield. T cells were depleted effectively, indicating excellent safety of the product. Characterization of the NK cells before and after cytokine activation revealed a notable increase in the expression of activation markers, particularly CD69, consistent with enhanced functionality. Intriguingly, the NK cells exhibited increased killing efficacy against patient-derived CD33 + AML blasts and NBL cells in vitro, suggesting a potential therapeutic benefit in AML and NBL.

Indexed as

Killer Cells, NaturalLeukemia, Myeloid, AcuteNeuroblastomaAntigens, Differentiation, T-LymphocyteCell Line, TumorCytokinesCytotoxicity, ImmunologicHumansInterleukin-15Interleukin-2LeukapheresisAntigens, Differentiation, T-LymphocyteCytokinesInterleukin-15Interleukin-2AML blastCliniMACS prodigyImmunotherapyNatural killer cells

Identifiers

PMID39496674
PMCPMC11535237

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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.