Evidence map›Paper›PMID 30542346›Full record

ArticleFrontiers in immunology2018

Enhancing the Activation and Releasing the Brakes: A Double Hit Strategy to Improve NK Cell Cytotoxicity Against Multiple Myeloma.

Sara Tognarelli, Sebastian Wirsching, Ivana von Metzler, Bushra Rais, Benedikt Jacobs, Hubert Serve, Peter Bader, Evelyn Ullrich

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

25 citing papers in PubMed, 33 citations in OpenAlex.

  1. Selinexor potentiates NK cell activation against multiple myeloma.Clinical and experimental immunology · 2026
    Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Regulation of CD38 on Multiple Myeloma and NK Cells by Monoclonal Antibodies.International journal of biological sciences · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. 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

8 authors at 2 institutions in 1 country.

Sara TognarelliChildrens Hospital, Experimental Immunology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Sebastian WirschingChildrens Hospital, Experimental Immunology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Ivana von MetzlerDepartment of Hematology and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Bushra RaisChildrens Hospital, Experimental Immunology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Benedikt JacobsDepartment of Haematology and Oncology, University Hospital Erlangen, Erlangen, Germany.
Hubert ServeDepartment of Hematology and Oncology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Peter BaderChildrens Hospital, Experimental Immunology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Evelyn UllrichChildrens Hospital, Experimental Immunology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Goethe University Frankfurt · DEUniversitätsklinikum Erlangen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are innate lymphocytes with a strong antitumor ability. In tumor patients, such as multiple myeloma (MM) patients, an elevated number of NK cells after stem cell transplantation (SCT) has been reported to be correlated with a higher overall survival rate. With the aim of improving NK cell use for adoptive cell therapy, we also addressed the cytotoxicity of patient-derived, cytokine-stimulated NK cells against MM cells at specific time points: at diagnosis and before and after autologous stem cell transplantation. Remarkably, after cytokine stimulation, the patients' NK cells did not significantly differ from those of healthy donors. In a small cohort of MM patients, we were able to isolate autologous tumor cells, and we could demonstrate that IL-2/15 stimulated autologous NK cells were able to significantly improve their killing capacity of autologous tumor cells. With the aim to further improve the NK cell killing capacity against MM cells, we investigated the potential use of NK specific check point inhibitors with focus on NKG2A because this inhibitory NK cell receptor was upregulated following

Indexed as

AdultAgedCytotoxicity, ImmunologicHematopoietic Stem Cell TransplantationHistocompatibility Antigens Class IHLA-E AntigensHumansInterferon-gammaInterleukin-15Interleukin-2Killer Cells, NaturalLymphocyte ActivationMiddle AgedMultiple MyelomaNK Cell Lectin-Like Receptor Subfamily CTransplantation, AutologousHistocompatibility Antigens Class IHLA-E AntigensInterferon-gammaInterleukin-15Interleukin-2NK Cell Lectin-Like Receptor Subfamily Cadoptive cell therapyautologous stem cell transplantationcheckpoint inhibitionmultiple myelomaNK cellsNKG2A blocking

Identifiers

PMID30542346
PMCPMC6277768
OpenAlexW2903059471

What OpenQuestion 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 OpenQuestion graph.