Evidence map›Paper›PMID 30361801›Full record

ReviewSeminars in immunopathology2019

Off-the-shelf cell therapy with induced pluripotent stem cell-derived natural killer cells.

Michelle L Saetersmoen, Quirin Hammer, Bahram Valamehr, Dan S Kaufman, Karl-Johan Malmberg

Abstract readReview
PubMed Publisher
In one paragraph

Review in Seminars in immunopathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers.

0numbers the graph read from it
0cells of the map it votes in
94citing 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

94 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Adoptive Cell Therapy from the Dish: Potentiating Induced Pluripotent Stem Cells.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    Review
  7. Review
  8. Review
  9. Article
  10. Practical immunomodulatory landscape of glioblastoma multiforme (GBM) therapy.Journal of the Egyptian National Cancer Institute · 2024
    Review
  11. Article
  12. Article
  13. Reprogramming natural killer cells for cancer therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Review
  14. NY-ESO-1 antigen: A promising frontier in cancer immunotherapy.Clinical and translational medicine · 2024
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Manufacturing CAR-NK against tumors: Who is the ideal supplier?Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  20. Review

34 more citing papers are in PubMed but not listed here.

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

5 authors.

Michelle L SaetersmoenThe KG Jebsen Center for Cancer Immunotherapy, University of Oslo, Oslo, Norway.
Quirin HammerDepartment of Medicine, Huddinge, Karolinska Institute, Solna, Sweden.
Bahram ValamehrFate Therapeutics Inc., San Diego, CA, USA.
Dan S KaufmanDepartment of Medicine, University of California San Diego, La Jolla, CA, USA.
Karl-Johan MalmbergThe KG Jebsen Center for Cancer Immunotherapy, University of Oslo, Oslo, Norway. k.j.malmberg@medisin.uio.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell therapy is emerging as a very promising therapeutic modality against cancer, spearheaded by the clinical success of chimeric antigen receptor (CAR) modified T cells for B cell malignancies. Currently, FDA-approved CAR-T cell products are based on engineering of autologous T cells harvested from the patient, typically using a central manufacturing facility for gene editing before the product can be delivered to the clinic and infused to the patients. For a broader implementation of advanced cell therapy and to reduce costs, it would be advantageous to use allogeneic "universal" cell therapy products that can be stored in cell banks and provided upon request, in a manner analogous to biopharmaceutical drug products. In this review, we outline a roadmap for development of off-the-shelf cell therapy based on natural killer (NK) cells derived from induced pluripotent stem cells (iPSCs). We discuss strategies to engineer iPSC-derived NK (iPSC-NK) cells for enhanced functional potential, persistence, and homing.

Indexed as

Cell- and Tissue-Based TherapyAnimalsCell MovementCellular ReprogrammingCytotoxicity, ImmunologicGenetic EngineeringHumansImmunotherapy, AdoptiveInduced Pluripotent Stem CellsKiller Cells, NaturalNeoplasmsReceptors, Antigen, T-CellReceptors, Chimeric AntigenT-Cell Antigen Receptor SpecificityReceptors, Antigen, T-CellReceptors, Chimeric AntigenCancer immunotherapyCell therapyChimeric antigen receptorInduced pluripotent stem cellsNatural killer cellsOff-the-shelf

Identifiers

What OpenQuestion holds

Textmetadata
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.