Evidence map›Paper›PMID 27645493›Full record

ArticleImmunology and cell biology2017

Distinctive expression of interleukin-23 receptor subunits on human Th17 and γδ T cells.

Bruce D Wines, May L Yap, Maree S Powell, Peck-Szee Tan, K Kerry Ko, Eva Orlowski, P Mark Hogarth

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Article in Immunology and cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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 2 institutions in 1 country.

Bruce D WinesCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
May L YapCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
Maree S PowellCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
Peck-Szee TanCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
K Kerry KoCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
Eva OrlowskiCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
P Mark HogarthCentre for Biomedical Research, Burnet Institute, Melbourne, Victoria, Australia.
Burnet Institute · AUUniversity of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interleukin-23 (IL-23) pathway, T helper 17 (Th17) cells and γδ T cells, which respond to IL-23, have major pro-inflammatory roles. We have used unique IL-23 receptor (IL-23R) subunit-specific monoclonal antibodies, X67 and X68, and IL-12 receptor beta-1 subunit (IL-12Rβ1) expression levels to evaluate the IL-23R complex on CD4 αβ TCR Th17 cells and on γδ T cells. Both IL-23R and IL-12Rβ1 subunits constitute the functional IL-23R. Expression of the IL-23R subunit by cultured Th17 cells was heterogeneous. Th17 cells expressed consistent high levels of the IL-12Rβ1 subunit, which appeared a better predictor of responsiveness to IL-23 than the expression of the IL-23R subunit. Moreover, sorting memory CD4 T cells by high IL-12Rβ1 expression selectively enriched cells committed to IL-17 production from the blood. IL-23R expression was also observed on freshly isolated and cultured γδ T cells and the cultured γδ T cells were not responsive to IL-23.

Indexed as

AnimalsAntibodies, MonoclonalCells, CulturedHumansImmunologic MemoryInterleukin-12 Receptor beta 1 SubunitMiceProtein SubunitsReceptors, Antigen, T-Cell, gamma-deltaReceptors, InterleukinTh17 CellsAntibodies, MonoclonalIL23R protein, humanInterleukin-12 Receptor beta 1 SubunitProtein SubunitsReceptors, Antigen, T-Cell, gamma-deltaReceptors, Interleukin

Identifiers

PMID27645493
OpenAlexW2521307068

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.