Evidence map›Paper›PMID 34675932›Full record

ArticleFrontiers in immunology2021

NK Cell Reconstitution After Autologous Hematopoietic Stem Cell Transplantation: Association Between NK Cell Maturation Stage and Outcome in Multiple Myeloma.

Ane Orrantia, Iñigo Terrén, Gabirel Astarloa-Pando, Carmen González, Alasne Uranga, Juan J Mateos-Mazón, Juan C García-Ruiz, Marta Riñón, Mercedes Rey, Silvia Pérez-Fernandez and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. 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
1.5field-weighted citation impact, top 18% 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, 23 citations in OpenAlex.

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  9. Targeting the myeloid microenvironment in neuroblastoma.Journal of experimental & clinical cancer research : CR · 2023
    Review
  10. MHC Class I Ligands of Rhesus Macaque Killer Cell Ig-like Receptors.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Article
  11. Review
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  14. iScience · 2022
    Article
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  16. 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

12 authors at 3 institutions in 1 country.

Ane OrrantiaImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Iñigo TerrénImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Gabirel Astarloa-PandoImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Carmen GonzálezBiodonostia Health Research Institute, Hematology and Hemotherapy Service, Donostia University Hospital, Donostia-San Sebastián, Spain.
Alasne UrangaBiodonostia Health Research Institute, Hematology and Hemotherapy Service, Donostia University Hospital, Donostia-San Sebastián, Spain.
Juan J Mateos-MazónHematological Cancer Group, Biocruces Bizkaia Health Research Institute, Hematology and Hemotherapy Service, Cruces University Hospital, Barakaldo, Spain.
Juan C García-RuizHematological Cancer Group, Biocruces Bizkaia Health Research Institute, Hematology and Hemotherapy Service, Cruces University Hospital, Barakaldo, Spain.
Marta RiñónRegulation of the Immune System Group, Biocruces Bizkaia Health Research Institute, Immunology Service, Cruces University Hospital, Barakaldo, Spain.
Mercedes ReyBiodonostia Health Research Institute, Immunology Service, Donostia University Hospital, Donostia-San Sebastián, Spain.
Silvia Pérez-FernandezScientific Coordination Facility, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Olatz ZenarruzabeitiaImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
Francisco BorregoImmunopathology Group, Biocruces Bizkaia Health Research Institute, Barakaldo, Spain.
BioCruces Health research Institute · ESBiogipuzkoa Health Research Institute · ESIkerbasque · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous hematopoietic stem cell transplantation (autoHSCT) is a standard of care for transplant-eligible patients with multiple myeloma (MM). Among factors that influence outcome after autoHSCT, it has been suggested that the number of natural killer (NK) cells plays an important role. However, the impact that different NK cell subsets and their phenotype could have in disease progression after autoHSCT are less clear. For this reason, we have phenotypically and functionally characterized NK cells during immune system reconstitution after autoHSCT in 54 MM patients. Shortly after leukocyte recovery, an extensive redistribution of NK cell subsets occurs in these patients. In addition, NK cells undergo a profound phenotypic change characterized, among others, by their increased proliferative capacity and immature phenotype. Importantly, MM patients who showed lower frequencies of the mature highly differentiated NKG2A-CD57+ NK cell subset at +30 and +100 days after autoHSCT experienced superior progression-free survival and had a longer time to the next treatment than those with higher frequencies. Our results provide significant insights into NK cell reconstitution after autoHSCT and suggest that the degree of NK cell maturation after autoHSCT affects the clinical outcome of MM patients treated with this therapeutic strategy.

Indexed as

Hematopoietic Stem Cell TransplantationAdultAgedCytotoxicity, ImmunologicFemaleHumansInterleukin-15Kaplan-Meier EstimateKiller Cells, NaturalMaleMiddle AgedMultiple MyelomaProportional Hazards ModelsTransplantation, AutologousTreatment OutcomeIL15 protein, humanInterleukin-15adaptive NK cellsautologous hematopoietic stem cell transplantationCD57IL-15multiple myelomaNK cell maturationNK cellsNKG2A

Identifiers

PMID34675932
PMCPMC8524090
OpenAlexW3203429737

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.