Evidence map›Paper›PMID 32245149›Full record

ReviewCells2020

NK cells and CD38: Implication for (Immuno)Therapy in Plasma Cell Dyscrasias.

Renato Zambello, Gregorio Barilà, Sabrina Manni, Francesco Piazza, Gianpietro Semenzato

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Alterations in the CD56International journal of molecular sciences · 2023
    Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

Renato ZambelloDepartment of Medicine (DIMED), Hematology and Clinical Immunology Section, University of Padova, 35128 Padova, Italy.
Gregorio BarilàDepartment of Medicine (DIMED), Hematology and Clinical Immunology Section, University of Padova, 35128 Padova, Italy.
Sabrina ManniDepartment of Medicine (DIMED), Hematology and Clinical Immunology Section, University of Padova, 35128 Padova, Italy.
Francesco PiazzaDepartment of Medicine (DIMED), Hematology and Clinical Immunology Section, University of Padova, 35128 Padova, Italy.
Gianpietro SemenzatoDepartment of Medicine (DIMED), Hematology and Clinical Immunology Section, University of Padova, 35128 Padova, Italy.
University of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy represents a promising new avenue for the treatment of multiple myeloma (MM) patients, particularly with the availability of Monoclonal Antibodies (mAbs) as anti-CD38 Daratumumab and Isatuximab and anti-SLAM-F7 Elotuzumab. Although a clear NK activation has been demonstrated for Elotuzumab, the effect of anti-CD38 mAbs on NK system is controversial. As a matter of fact, an initial reduction of NK cells number characterizes Daratumumab therapy, limiting the potential role of this subset on myeloma immunotherapy. In this paper we discuss the role of NK cells along with anti-CD38 therapy and their implication in plasma cell dyscrasias, showing that mechanisms triggered by anti-CD38 mAbs ultimately lead to the activation of the immune system against myeloma cell growth.

Indexed as

ImmunotherapyADP-ribosyl Cyclase 1HumansKiller Cells, NaturalParaproteinemiasADP-ribosyl Cyclase 1CD38multiple myelomaNK cells

Identifiers

PMID32245149
PMCPMC7140687
OpenAlexW3012031746

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.