Evidence map›Paper›PMID 24363794›Full record

ArticlePloS one2013

The metalloprotease ADAM12 regulates the effector function of human Th17 cells.

Angela X Zhou, Aimee El Hed, Frances Mercer, Lina Kozhaya, Derya Unutmaz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 38% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. ADAM9 enhances Th17 cell differentiation and autoimmunity by activating TGF-β1.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  8. Article
  9. Article
  10. 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.

Angela X ZhouDepartment of Microbiology, New York University School of Medicine, New York, New York, United States of America.
Aimee El HedDepartment of Microbiology, New York University School of Medicine, New York, New York, United States of America.
Frances MercerDepartment of Microbiology, New York University School of Medicine, New York, New York, United States of America.
Lina KozhayaDepartment of Microbiology, New York University School of Medicine, New York, New York, United States of America.
Derya UnutmazDepartment of Microbiology, New York University School of Medicine, New York, New York, United States of America ; Department of Pathology, New York University School of Medicine, New York, New York, United States of America ; Department of Medicine, New York University School of Medicine, New York, New York, United States of America.
New York University · US

Funding

TRAINING PROGRAM: MECHANISMS OF VIRUS-HOST INTERACTIONST32AI007647 · NIAID · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI Domenico Tortorella · 2000 to 2026
$11.5M
INFECTIOUS DISEASES &BASIC MICROBIOLOGICAL MECHANISMST32AI007180 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WEISER, JEFFREY NEAL · 1985 to 2022
$8.9M
Immunobiology of Regulatory T Cells in HIV InfectionR01AI065303 · NIAID · VANDERBILT UNIVERSITY · PI UNUTMAZ, DERYA · 2005 to 2015
$4.3M
Role and Perturbation of Th17 Cells During HIV InfectionR21AI087973 · NIAID · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI UNUTMAZ, DERYA · 2010 to 2011
$462k
NIAID NIH HHS 5T32AI007647NIAID NIH HHS R01 AI065303NIAID NIH HHS R01AI065303NIAID NIH HHS R21 AI087973NIAID NIH HHS R21AI087973NIAID NIH HHS T32 AI007180NIAID NIH HHS T32 AI007647
6 · The paper itself

Abstract

A key modulator of immune homeostasis, TGFβ has an important role in the differentiation of regulatory T cells (Tregs) and IL-17-secreting T cells (Th17). How TGFβ regulates these functionally opposing T cell subsets is not well understood. We determined that an ADAM family metalloprotease called ADAM12 is specifically and highly expressed in both Tregs and CCR6+ Th17 cells. ADAM12 is induced in vitro upon differentiation of naïve T cells to Th17 cells or IL-17-secreting Tregs. Remarkably, silencing ADAM12 expression in CCR6+ memory T cells enhances the production of Th17 cytokines, similar to suppressing TGFβ signaling. Further, ADAM12 knockdown in naïve human T cells polarized towards Th17/Treg cells, or ectopically expressing RORC, greatly enhances IL-17-secreting cell differentiation, more potently then inhibiting TGFβ signals. Together, our findings reveal a novel regulatory role for ADAM12 in Th17 cell differentiation or function and may have implications in regulating their aberrant responses during immune pathologies.

Indexed as

ADAM12 ProteinADAM ProteinsCD4-Positive T-LymphocytesCell DifferentiationCells, CulturedHumansInterleukin-17Membrane ProteinsReceptors, CCR6Reverse Transcriptase Polymerase Chain ReactionTh17 CellsT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsADAM12 ProteinADAM12 protein, humanADAM ProteinsCCR6 protein, humanInterleukin-17Membrane ProteinsReceptors, CCR6

Identifiers

PMID24363794
PMCPMC3867213
OpenAlexW1993362788

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.