Evidence map›Paper›PMID 30953117›Full record

ReviewCancer immunology, immunotherapy : CII2019

Modulation of NK cells with checkpoint inhibitors in the context of cancer immunotherapy.

Beatriz Sanchez-Correa, Nelson Lopez-Sejas, Esther Duran, Fernando Labella, Corona Alonso, Rafael Solana, Raquel Tarazona

Open access · greenAbstract readReview
In one paragraph

Review in Cancer immunology, immunotherapy : CII, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

38 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Human NK cells and cancer.Oncoimmunology · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Circular RNAs in hepatocellular carcinoma: Recent advances.World journal of gastrointestinal oncology · 2022
    Review
  18. Article
  19. Review
  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

7 authors at 3 institutions in 1 country.

Beatriz Sanchez-CorreaImmunology Unit, University of Extremadura, Caceres, Spain.
Nelson Lopez-SejasImmunology Unit, University of Extremadura, Caceres, Spain.
Esther DuranHistology and Pathology Unit, Faculty of Veterinary, University of Extremadura, Caceres, Spain.
Fernando LabellaImmunology Unit, Universidad de Cordoba, Cordoba, Spain.
Corona AlonsoInstituto Maimónides de Investigación Biomédica (IMIBIC), Córdoba, Spain.
Rafael SolanaImmunology Unit, Universidad de Cordoba, Cordoba, Spain. rsolana@uco.es.ORCID http://orcid.org/0000-0001-8985-0295
Raquel TarazonaImmunology Unit, University of Extremadura, Caceres, Spain.
Universidad de Extremadura · ESInstituto Maimónides de Investigación Biomédica de Córdoba · ESUniversity of Córdoba · ES

Funding

Epidemiology of Ovarian Cancer:New HypothesesR01CA087538 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ROSSING, MARY ANNE · 2002 to 2006
$3.5M
VARIAN DMS 200 UV-VIS SPECTROPHOTOMETERS15CA046161 · NCI · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI TEWKSBURY, DUANE A · 1987 to 1987
–
Agencia Estatal de Investigación SAF2013-46161-RAgencia Estatal de Investigación SAF2017-87538-RConsejería de Economia e Infraestructura. Junta de Extremadura (ES) GR18085Consejería de Economia e Infraestructura. Junta de Extremadura (ES) IB16164Instituto de Salud Carlos III (ES) PI13/02691Instituto de Salud Carlos III (ES) PI16/01615
6 · The paper itself

Abstract

The incidence of some types of tumours has increased progressively in recent years and is expected to continue growing in the coming years due in part to the aging of the population. The design of new therapies based on natural killer (NK) cells opens new possibilities especially for the treatment of elderly patients who are particularly susceptible to the toxicity of conventional chemotherapy treatments. In recent years, the potential use of NK cells in cancer immunotherapy has been of great interest thanks to advances in the study of NK cell biology. The identification of key points (checkpoints) in the activation of NK cells that can be regulated by monoclonal antibodies has allowed the design of new therapeutic strategies based on NK cells. However, there are still limitations for its use and the first clinical trials blocking KIR inhibitory receptors have shown little efficacy by inhibiting the maturation of NK cells. Blockade of other inhibitory receptors such as TIGIT, TIM3, LAG3 and PD1 may represent novel strategies to increase NK function in cancer patients. Altogether, the identification of NK cell and tumour cell markers of resistance or susceptibility to the action of NK cells will contribute to identifying those patients that will most likely benefit from NK cell-based immunotherapy.

Indexed as

AnimalsAntibodies, MonoclonalCostimulatory and Inhibitory T-Cell ReceptorsHumansImmunomodulationImmunotherapyKiller Cells, NaturalNeoplasmsAntibodies, MonoclonalCostimulatory and Inhibitory T-Cell ReceptorsCheckpoint blockadeImmunotherapymiRNANK cellsPIVAC 17

Identifiers

PMID30953117
PMCPMC11028212
OpenAlexW2931041341

What OpenQuestion holds

Textmetadata
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.