Evidence map›Paper›PMID 28235773›Full record

ArticleJournal of leukocyte biology2017

TLR10 suppresses the activation and differentiation of monocytes with effects on DC-mediated adaptive immune responses.

Nicholas J Hess, Christopher Felicelli, Jennifer Grage, Richard I Tapping

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
  2. Observational
  3. Updates on Toll-Like Receptor 10 Research.European journal of immunology · 2025
    Review
  4. Article
  5. Article
  6. Role of Innate Immunity in Allergic Contact Dermatitis: An Update.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Toll-like receptor-agonist-based therapies for respiratory viral diseases: thinking outside the cell.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Expression and Function of Toll-Like Receptor 10 (TLR10) in Diffuse Large B Cell Lymphoma, Acute Myeloid Leukemia, and Glioma.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

Nicholas J HessDepartment of Microbiology, University of Illinois, Urbana-Champaign, Illinois, USA; and.
Christopher FelicelliDepartment of Microbiology, University of Illinois, Urbana-Champaign, Illinois, USA; and.
Jennifer GrageDepartment of Microbiology, University of Illinois, Urbana-Champaign, Illinois, USA; and.
Richard I TappingDepartment of Microbiology, University of Illinois, Urbana-Champaign, Illinois, USA; and tapping@illinois.edu.
University of Illinois Urbana-Champaign · US

Funding

Regulation of B cell lymphocyte responses by TLR10R01AI097639 · NIAID · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI TAPPING, RICHARD IAN · 2012 to 2016
$1.9M
NIAID NIH HHS R01 AI097639
6 · The paper itself

Abstract

TLRs are important pattern-recognition receptors involved in the activation of innate immune responses against foreign pathogens. TLR10 is the only TLR family member without a known ligand, signaling pathway, or clear cellular function. Previous work has shown that TLR10 suppresses proinflammatory cytokine production in response to TLR agonists in a mixed human mononuclear cell population. We report that TLR10 is preferentially expressed on monocytes and suppresses proinflammatory cytokine production resulting from either TLR or CD40 stimulation. TLR10 engagement affects both the MAPK and Akt signaling pathways, leading to changes in the transcriptome of isolated human monocytes. Differentiation of monocytes into dendritic cells in the presence of an αTLR10 mAb reduced the expression of maturation markers and the induction of proinflammatory cytokines, again in response to either TLR or CD40 stimulation. Finally, in coculture experiments, TLR10 differentiated dendritic cells exhibited a decreased capacity to activate T cells as measured by IL-2 and IFN-γ production. These data demonstrate that TLR10 is a novel regulator of innate immune responses and of the differentiation of primary human monocytes into effective dendritic cells.

Indexed as

Adaptive ImmunityAntibodies, MonoclonalCD40 AntigensCell DifferentiationCoculture TechniquesDendritic CellsGene Expression RegulationHumansImmunity, InnateInterferon-gammaInterleukin-2Mitogen-Activated Protein KinasesMonocytesPrimary Cell CultureProto-Oncogene Proteins c-aktSignal TransductionAntibodies, MonoclonalCD40 AntigensIFNG protein, humanInterferon-gammaInterleukin-2Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-aktTLR10 protein, humanToll-Like Receptor 10cytokinesregulationTLR

Identifiers

PMID28235773
PMCPMC5380377
OpenAlexW2590444212

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.