Evidence map›Paper›PMID 35091452›Full record

ArticleJournal for immunotherapy of cancer2022

Toll-like receptor 8 agonists improve NK-cell function primarily targeting CD56

Irene Veneziani, Claudia Alicata, Andrea Pelosi, Nadine Landolina, Biancamaria Ricci, Valentina D'Oria, Anna Fagotti, Giovanni Scambia, Lorenzo Moretta, Enrico Maggi

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Harnessing innate immune pathways for therapeutic advancement in cancer.Signal transduction and targeted therapy · 2024
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Irene Veneziani *Department of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.ORCID 0000-0002-1243-3757
Claudia Alicata *Department of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.
Andrea PelosiDepartment of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.ORCID 0000-0003-2308-9215
Nadine LandolinaDepartment of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.
Biancamaria RicciDepartment of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.
Valentina D'OriaConfocal Microscopy Core Facility, Bambino Gesu Pediatric Hospital, Roma, Italy.
Anna FagottiDepartment of Woman's Health Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.
Giovanni ScambiaDepartment of Woman's Health Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.
Lorenzo MorettaDepartment of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy.
Enrico MaggiDepartment of Immunology, Bambino Gesu Pediatric Hospital, Roma, Italy enrico.maggi@opbg.net.
Bambino Gesù Children's Hospital · ITUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundToll-like receptors (TLRs) are pattern-recognition sensors mainly expressed in innate immune cells that directly recognize conserved pathogen structures (pathogen-associated molecular patterns-PAMPs). Natural killer (NK) cells have been described to express different endosomal TLRs triggered by RNA and DNA sequences derived from both viruses and bacteria. This study was addressed to establish which endosomal TLR could directly mediate NK activation and function after proper stimuli. It was also important to establish the most suitable TLR agonist to be used as adjuvant in tumor vaccines or in combined cancer immunotherapies.

methodsWe assessed endosomal TLR expression in total NK cells by using RT-qPCR and western blotting technique. In some experiments, we purified CD56

resultsAlthough the four endosomal TLRs (TLR3, TLR7/8, and TLR9) were uniformly expressed on CD56

conclusionThese data highlight the potential value of TLR8 in NK cells as a new target for immunotherapy in patients with cancer.

Indexed as

CD56 AntigenCell Line, TumorCytokinesCytotoxicity, ImmunologicFemaleGPI-Linked ProteinsHumansImidazolesKiller Cells, NaturalOvarian NeoplasmsReceptors, IgGToll-Like Receptor 8CD56 AntigenCytokinesFCGR3B protein, humanGPI-Linked ProteinsImidazolesNCAM1 protein, humanReceptors, IgGresiquimodToll-Like Receptor 8adjuvantsimmunologicimmunotherapykiller cellsnaturalreceptorstumor microenvironment

Identifiers

PMID35091452
PMCPMC8804697
OpenAlexW4210497205

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.