Evidence map›Paper›PMID 32708751›Full record

ArticleCancers2020

Genetic and Molecular Basis of Heterogeneous NK Cell Responses against Acute Leukemia.

Dhon Roméo Makanga, Francesca Da Rin de Lorenzo, Gaëlle David, Catherine Willem, Léa Dubreuil, Nolwenn Legrand, Thierry Guillaume, Pierre Peterlin, Amandine Lebourgeois, Marie Christine Béné and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. 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

17 authors at 4 institutions in 2 countries.

Dhon Roméo MakangaEtablissement Français du Sang, 44011 Nantes, France.
Francesca Da Rin de LorenzoEtablissement Français du Sang, 44011 Nantes, France.
Gaëlle DavidEtablissement Français du Sang, 44011 Nantes, France.
Catherine WillemEtablissement Français du Sang, 44011 Nantes, France.
Léa DubreuilEtablissement Français du Sang, 44011 Nantes, France.
Nolwenn LegrandEtablissement Français du Sang, 44011 Nantes, France.
Thierry GuillaumeUniversité de Nantes, INSERM U1232 CNRS, CRCINA, F-44000 Nantes, France.
Pierre PeterlinHematology Clinic, CHU, 44000 Nantes, France.
Amandine LebourgeoisHematology Clinic, CHU, 44000 Nantes, France.
Marie Christine BénéUniversité de Nantes, INSERM U1232 CNRS, CRCINA, F-44000 Nantes, France.
Alice GarnierHematology Clinic, CHU, 44000 Nantes, France.
Patrice ChevallierUniversité de Nantes, INSERM U1232 CNRS, CRCINA, F-44000 Nantes, France.
Ketevan GendzekhadzeHLA Laboratory, Department of Hematology and HCT, City of Hope, Medical Center, Duarte, CA 91010, USA.
Anne CesbronEtablissement Français du Sang, 44011 Nantes, France.
Katia GagneEtablissement Français du Sang, 44011 Nantes, France.
Béatrice ClemenceauUniversité de Nantes, INSERM U1232 CNRS, CRCINA, F-44000 Nantes, France.
Christelle RetièreEtablissement Français du Sang, 44011 Nantes, France.ORCID 0000-0001-5943-6990
Centre National de la Recherche Scientifique · FRCentre Hospitalier Universitaire de Nantes · FRCity Of Hope National Medical Center · USÉtablissement Français du Sang · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells are key cytotoxic effectors against malignant cells. Polygenic and polymorphic Killer cell Immunoglobulin-like Receptor (KIR) and HLA genes participate in the structural and functional formation of the NK cell repertoire. In this study, we extensively investigated the anti-leukemic potential of NK cell subsets, taking into account these genetic parameters and cytomegalovirus (CMV) status. Hierarchical clustering analysis of NK cell subsets based on NKG2A, KIR, CD57 and NKG2C markers from 68 blood donors identified donor clusters characterized by a specific phenotypic NK cell repertoire linked to a particular immunogenetic KIR and HLA profile and CMV status. On the functional side, acute lymphoblastic leukemia (ALL) was better recognized by NK cells than acute myeloid leukemia (AML). However, a broad inter-individual disparity of NK cell responses exists against the same leukemic target, highlighting bad and good NK responders. The most effective NK cell subsets against different ALLs expressed NKG2A and represented the most frequent subset in the NK cell repertoire. In contrast, minority CD57

Indexed as

acute leukemiaCMVHLAKIRnatural killer cellsrepertoire

Identifiers

PMID32708751
PMCPMC7409189
OpenAlexW3042504484

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.