Evidence map›Paper›PMID 28824651›Full record

ArticleFrontiers in immunology2017

Beatriz Sanchez-Correa, Juan M Bergua, Alejandra Pera, Carmen Campos, Maria Jose Arcos, Helena Bañas, Esther Duran, Rafael Solana, Raquel Tarazona

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Reduction of CaCells · 2023
    Article
  6. Article
  7. Review
  8. CAR-T Cell Therapy for Acute Myeloid Leukemia: Preclinical Rationale, Current Clinical Progress, and Barriers to Success.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Observational
  16. Review
  17. NK Cell Plasticity in Cancer.Journal of clinical medicine · 2019
    Review
  18. Review
  19. Review
  20. On the Way to Become a Natural Killer Cell.Frontiers in immunology · 2019
    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

9 authors at 3 institutions in 2 countries.

Beatriz Sanchez-CorreaImmunology Unit, University of Extremadura, Cáceres, Spain.
Juan M BerguaDepartment of Haematology, Hospital San Pedro de Alcantara, Cáceres, Spain.
Alejandra PeraInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba, Red Espanola de Investigacion en Patologia Infecciosa (REIPI), Córdoba, Spain.
Carmen CamposInstituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC), Reina Sofia University Hospital, University of Cordoba, Red Espanola de Investigacion en Patologia Infecciosa (REIPI), Córdoba, Spain.
Maria Jose ArcosDepartment of Haematology, Hospital San Pedro de Alcantara, Cáceres, Spain.
Helena BañasDepartment of Haematology, Hospital San Pedro de Alcantara, Cáceres, Spain.
Esther DuranHistology and Pathology Unit, Faculty of Veterinary, University of Extremadura, Cáceres, Spain.
Rafael SolanaImmunology Unit, University of Extremadura, Cáceres, Spain.
Raquel TarazonaImmunology Unit, University of Extremadura, Cáceres, Spain.
Hospital San Pedro de Alcántara · ESUniversidad de Extremadura · ESUniversity of Córdoba · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite recent progress in the therapeutic approach of malignant hemopathies, their prognoses remain frequently poor. Immunotherapy could open a new window of great interest in this setting. Natural killer (NK) cells constitute an important area of research for hematologic malignancies, because this subpopulation is able to kill target cells spontaneously without previous sensitization, representing a novel tool in the treatment of them. Abnormal NK cytolytic function is observed in several hematological malignancies, including acute myeloid leukemia (AML) and myelodysplastic syndromes. Several mechanisms are involved in this abnormal function, such as decreased expression of activating receptors, increased expression of inhibitory receptors or defective expression of NK cell ligands on target cells. New immunotherapies are focused in identifying factors that could increase the expression of these activating receptors, to counteract inhibitory receptors expression, and therefore, to improve the NK cell cytotoxic capacities against tumor cells. In this work, we analyze the effect of interleukin (IL)-15 on the expression of NK cell-activating receptors that play a crucial role in the lysis of blasts from AML patients. Our results showed that IL-15 increased the surface expression of NKp30 on NK cells from healthy donors and AML patients with the consequent improvement of NK cell cytotoxicity. Besides, the upregulation of NKp30 induced by IL-15 is associated with an improvement of NK-mediated myeloid dendritic cells (DCs) maturation. NK cells cultured with IL-15 showed an upregulation of NKp30, which is associated with an increase anti-tumor activity and with an improved maturation of immature DCs. In our

Indexed as

acute myeloid leukemiadendritic cellsinterleukin-15natural killer cellnatural killer cell degranulationNKp30

Identifiers

PMID28824651
PMCPMC5545593
OpenAlexW2742727395

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.