Evidence map›Paper›PMID 27101876›Full record

ArticleMolecules and cells2016

PLZF(+) Innate T Cells Support the TGF-β-Dependent Generation of Activated/Memory-Like Regulatory T Cells.

Byung Hyun Kang, Hyo Jin Park, Hi Jung Park, Jae-Ii Lee, Seong Hoe Park, Kyeong Cheon Jung

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2016. 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
0.5field-weighted citation impact, top 34% 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, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Myeloid cells activate iNKT cells to produce IL-4 in the thymic medulla.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  7. Article
  8. 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

6 authors at 2 institutions in 1 country.

Byung Hyun KangPostgraduate Course of Translational Medicine, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Hyo Jin ParkDepartment of Pathology, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Hi Jung ParkPostgraduate Course of Translational Medicine, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Jae-Ii LeePostgraduate Course of Translational Medicine, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Seong Hoe ParkPostgraduate Course of Translational Medicine, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Kyeong Cheon JungPostgraduate Course of Translational Medicine, Medical Research Center, Seoul National University College of Medicine, Seoul 03080, Korea.
Seoul National University Hospital · KRSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PLZF-expressing invariant natural killer T cells and CD4 T cells are unique subsets of innate T cells. Both are selected via thymocyte-thymocyte interaction, and they contribute to the generation of activated/memory-like CD4 and CD8 T cells in the thymus via the production of IL-4. Here, we investigated whether PLZF(+) innate T cells also affect the development and function of Foxp3(+) regulatory CD4 T cells. Flow cytometry analysis of the thymus and spleen from both CIITA transgenic C57BL/6 and wild-type BALB/c mice, which have abundant PLZF(+) CD4 T cells and invariant natural killer T cells, respectively, revealed that Foxp3(+) T cells in these mice exhibited a CD103(+) activated/memory-like phenotype. The frequency of CD103(+) regulatory T cells was considerably decreased in PLZF(+) cell-deficient CIITA(Tg)Plzf(lu/lu) and BALB/c.CD1d(-/-) mice as well as in an IL-4-deficient background, such as in CIITA(Tg)IL-4(-/-) and BALB/c.lL-4(-/-) mice, indicating that the acquisition of an activated/memory-like phenotype was dependent on PLZF(+) innate T cells and IL-4. Using fetal thymic organ culture, we further demonstrated that IL-4 in concert with TGF-β enhanced the acquisition of the activated/memory-like phenotype of regulatory T cells. In functional aspects, the activated/memory-like phenotype of Treg cells was directly related to their suppressive function; regulatory T cells of CIITA(Tg)PIV(-/-) mice more efficiently suppressed ovalbumin-induced allergic airway inflammation compared with their counterparts from wild-type mice. All of these findings suggest that PLZF(+) innate T cells also augmented the generation of activated/memory-like regulation via IL-4 production.

Indexed as

Immunity, InnateAnimalsCD4-Positive T-LymphocytesForkhead Transcription FactorsInterleukin-4Kruppel-Like Transcription FactorsLymphocyte ActivationMiceMice, Inbred BALB CMice, Inbred C57BLNatural Killer T-CellsOrgan Culture TechniquesPhenotypePromyelocytic Leukemia Zinc Finger ProteinSpleenThymus GlandForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-4Kruppel-Like Transcription FactorsPromyelocytic Leukemia Zinc Finger ProteinTransforming Growth Factor betaZbtb16 protein, mouseIL-4PLZFregulatory T lymphocyte

Identifiers

PMID27101876
PMCPMC4916398
OpenAlexW2338526062

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.