Evidence map›Paper›PMID 27194790›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

Direct TLR-2 Costimulation Unmasks the Proinflammatory Potential of Neonatal CD4+ T Cells.

Brian D Sinnott, Byung Park, Mardi C Boer, Deborah A Lewinsohn, Christina L Lancioni

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Bystander CD4Experimental & molecular medicine · 2020
    Review
  14. Review
  15. Neonatal T Cells: A Reinterpretation.Annual review of immunology · 2020
    Review
  16. Article
  17. Observational
  18. Article
  19. Article
  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

5 authors at 1 institution in 1 country.

Brian D SinnottDepartment of Pediatrics, Oregon Health & Science University, Portland, OR 97239; and.
Byung ParkDivision of Biostatistics, Department of Public Health and Preventive Medicine, Oregon Health & Science University, Portland, OR 97239.ORCID 0000-0003-3516-7516
Mardi C BoerDepartment of Pediatrics, Oregon Health & Science University, Portland, OR 97239; and.
Deborah A LewinsohnDepartment of Pediatrics, Oregon Health & Science University, Portland, OR 97239; and.
Christina L LancioniDepartment of Pediatrics, Oregon Health & Science University, Portland, OR 97239; and lancioni@ohsu.edu.
Oregon Health & Science University · US

Funding

The innate capacity of human T cells to respond to Mycobacterium tuberculosisR01AI104229 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DEBORAH A. · 2013 to 2016
$1.5M
Tuberculosis Immunity in Young ChildrenR01AI054474 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DEBORAH A. · 2003 to 2006
$1.3M
MTB directly regulates human CD4+ T cell activationK08AI083739 · NIAID · OREGON HEALTH & SCIENCE UNIVERSITY · PI LANCIONI, CHRISTINA LOUISE · 2009 to 2013
$637k
NIAID NIH HHS K08 AI083739NIAID NIH HHS R01 AI054474NIAID NIH HHS R01 AI104229
6 · The paper itself

Abstract

Neonatal CD4(+) T cells have traditionally been viewed as deficient in their capacity to produce Th1 cytokines in response to polyclonal or Ag-specific stimuli. Thus, defining unique aspects of CD4(+) T cell activation and development into Th1 effector cells in neonates is essential to the successful development of novel vaccines and immunotherapies to protect infants from intracellular pathogens. Using highly purified naive CD4(+) T cells derived from cord and adult peripheral blood, we compared the impact of anti-CD3 stimulation plus costimulation through TLR-2 performed in the absence of APC on CD4(+) T cell cytokine production, proliferation, and expression of activation markers. In both age groups, TLR-2 costimulation elicited activation of naive CD4(+) T cells, characterized by robust production of IL-2 as well as key Th1-type cytokines IFN-γ and TNF-α. TLR-2 costimulation also dramatically reduced naive T cell production of the immunosuppressive cytokine IL-10. We observed that neonatal naive CD4(+) T cells are uniquely sensitive to TLR-2-mediated costimulation, which enabled them to produce equivalent amounts of IFN-γ and more IL-2 when compared with adult responses. Thus, neonatal CD4(+) T cells have a distinctive propensity to use TLR-2-mediated costimulation for development into proinflammatory Th1 effectors, and interventions that target CD4(+) T cell TLR-2-mediated responses may be exploited to enhance neonatal adaptive immunity.

Indexed as

AdolescentAdultAgedCell DifferentiationCell ProliferationCells, CulturedCytokinesFemaleFetal BloodHumansInfant, NewbornInflammation MediatorsLymphocyte ActivationMaleMiddle AgedTh1 CellsCytokinesInflammation MediatorsTLR2 protein, humanToll-Like Receptor 2

Identifiers

PMID27194790
PMCPMC5023071
OpenAlexW2399560959

What OpenQuestion holds

Textmetadata
LicenceTDM
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.