Evidence map›Paper›PMID 39000607›Full record

ArticleInternational journal of molecular sciences2024

TLR Agonists Modify NK Cell Activation and Increase Its Cytotoxicity in Acute Lymphoblastic Leukemia.

Janet Gallardo-Zapata, Erandi Pérez-Figueroa, Víctor Olivar-López, Aurora Medina-Sansón, Elva Jiménez-Hernández, Enrique Ortega, Carmen Maldonado-Bernal

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Modulation of NK Cell Properties by ESKAPE Group Bacteria.International journal of molecular sciences · 2025
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. 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

7 authors.

Janet Gallardo-ZapataImmunology and Proteomics Research Laboratory, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.
Erandi Pérez-FigueroaImmunology and Proteomics Research Laboratory, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.
Víctor Olivar-LópezEmergency Service, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.
Aurora Medina-SansónHemato-Oncology Department, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.
Elva Jiménez-HernándezHematology Service, Hospital Pediátrico Moctezuma, Mexico City 15530, Mexico.
Enrique OrtegaDepartment of Immunology, Institute of Biomedical Research, Universidad Nacional Autónoma de México, Mexico City 4510, Mexico.
Carmen Maldonado-BernalImmunology and Proteomics Research Laboratory, Hospital Infantil de México Federico Gómez, Mexico City 06720, Mexico.ORCID 0000-0003-0663-2888

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK) cells play a crucial role in innate immunity, particularly in combating infections and tumors. However, in hematological cancers, NK cells often exhibit impaired functions. Therefore, it is very important to activate its endosomal Toll-like receptors (TLRs) as a potential strategy to restore its antitumor activity. We stimulated NK cells from the peripheral blood mononuclear cells from children with acute lymphoblastic leukemia and NK cells isolated, and the NK cells were stimulated with specific TLR ligands (Poly I:C, Imiquimod, R848, and ODN2006) and we evaluated changes in IFN-γ, CD107a, NKG2D, NKp44 expression, Granzyme B secretion, cytokine/chemokine release, and cytotoxic activity. Results revealed that Poly I:C and Imiquimod enhanced the activation of both immunoregulatory and cytotoxic NK cells, increasing IFN-γ, CD107a, NKG2D, and NKp44 expression. R848 activated immunoregulatory NK cells, while ODN2006 boosted CD107a, NKp44, NKG2D, and IFN-γ secretion in cytotoxic NK cells. R848 also increased the secretion of seven cytokines/chemokines. Importantly, R848 and ODN 2006 significantly improved cytotoxicity against leukemic cells. Overall, TLR stimulation enhances NK cell activation, suggesting TLR8 (R848) and TLR9 (ODN 2006) ligands as promising candidates for antitumor immunotherapy.

Indexed as

ImiquimodKiller Cells, NaturalLymphocyte ActivationPoly I-CPrecursor Cell Lymphoblastic Leukemia-LymphomaToll-Like ReceptorsChildChild, PreschoolCytokinesCytotoxicity, ImmunologicFemaleHumansImidazolesInterferon-gammaMaleOligodeoxyribonucleotidesCytokinesImidazolesImiquimodInterferon-gammaOligodeoxyribonucleotidesPoly I-CresiquimodToll-Like Receptor AgonistsToll-Like Receptorsacute lymphoblastic leukemiacytotoxicityIFN-γnatural killer cellsNKG2DNKp44toll-like receptors

Identifiers

PMID39000607
PMCPMC11242025

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.