Evidence map›Paper›PMID 31214182›Full record

ArticleFrontiers in immunology2019

Improving Clinical Manufacturing of IL-15 Activated Cytokine-Induced Killer (CIK) Cells.

Melanie Bremm, Lisa-Marie Pfeffermann, Claudia Cappel, Verena Katzki, Stephanie Erben, Sibille Betz, Andrea Quaiser, Michael Merker, Halvard Bonig, Michael Schmidt and 4 more

Abstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  6. Cytokine-Induced Killer Cells: A Unique Platform for Adoptive Cell Immunotherapy after Allogeneic Hematopoietic Stem Cell Transplantation.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    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

14 authors.

Melanie BremmClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Lisa-Marie PfeffermannClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Claudia CappelClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Verena KatzkiClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Stephanie ErbenClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Sibille BetzClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Andrea QuaiserDepartment of Cell Therapy, Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig, Germany.
Michael MerkerClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Halvard BonigDivision for Translational Development of Cellular Therapeutics, Institute for Transfusion Medicine and Immunohematology, Goethe-University Frankfurt, Frankfurt, Germany.
Michael SchmidtDivision for Translational Development of Cellular Therapeutics, Institute for Transfusion Medicine and Immunohematology, Goethe-University Frankfurt, Frankfurt, Germany.
Thomas KlingebielClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Peter BaderClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Sabine HueneckeClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.
Eva RettingerClinic for Pediatric and Adolescent Medicine, University Hospital, Frankfurt, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cytokine-induced killer (CIK) cells are an immunotherapeutic approach to combat relapse following allogeneic hematopoietic stem cell transplantation (HSCT) in acute leukemia or myelodysplastic syndrome (MDS) patients. Prompt and sequential administration of escalating cell doses improves the efficacy of CIK cell therapy without exacerbating graft vs. host disease (GVHD). This study addresses manufacturing-related issues and aimed to develop a time-, personal- and cost-saving good manufacturing process (GMP)-compliant protocol for the generation of ready-for-use therapeutic CIK cell doses starting from one unstimulated donor-derived peripheral blood (PB) or leukocytapheresis (LP) products. Culture medium with or without the addition of either AB serum, fresh frozen plasma (FFP) or platelet lysate (PL) was used for culture. Fresh and cryopreserved CIK cells were compared regarding expansion rate, viability, phenotype, and ability to inhibit leukemia growth. Cell numbers increased by a median factor of 10-fold in the presence of FFP, PL, or AB serum, whereas cultivation in FFP/PL-free or AB serum-free medium failed to promote adequate CIK cell proliferation (

Indexed as

Cell Culture TechniquesCell ProliferationCells, CulturedCryopreservationCytokine-Induced Killer CellsCytotoxicity, ImmunologicGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunotherapy, AdoptiveInterleukin-15Leukemia, Biphenotypic, AcuteMyelodysplastic SyndromesPlasmaTransplantation, HomologousInterleukin-15AB-serumallogeneic stem cell transplantationCIK cellscryopreservationfresh frozen plasmaimmunotherapyplatelet lysate

Identifiers

PMID31214182
PMCPMC6554420

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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 OpenQuestion graph.