Evidence map›Paper›PMID 20194631›Full record

ArticleThe Journal of experimental medicine2010

CCR6 is expressed on an IL-10-producing, autoreactive memory T cell population with context-dependent regulatory function.

Laura Rivino, Paola Gruarin, Barbara Häringer, Svenja Steinfelder, Laura Lozza, Bodo Steckel, Anja Weick, Elisa Sugliano, David Jarrossay, Anja A Kühl and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

34 citing papers in PubMed, 65 citations in OpenAlex.

  1. Regulatory T cells in the skin: Origin, function, and plasticity.JID innovations : skin science from molecules to population health · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Human CCR6bioRxiv : the preprint server for biology · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Dual Role of Interleukin-10 in Murine NZB/W F1 Lupus.International journal of molecular sciences · 2021
    Article
  10. Article
  11. Article
  12. Evidence for a pathogenic role of extrafollicular, IL-10-producing CCR6Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Article
  14. Delivery of IL-35 byFrontiers in immunology · 2018
    Article
  15. Article
  16. Review
  17. Article
  18. Review
  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

15 authors at 4 institutions in 2 countries.

Laura RivinoInstitute for Research in Biomedicine, Bellinzona, Switzerland.
Paola Gruarin
Barbara Häringer
Svenja Steinfelder
Laura Lozza
Bodo Steckel
Anja Weick
Elisa Sugliano
David Jarrossay
Anja A Kühl
Christoph Loddenkemper
Sergio Abrignani
Federica Sallusto
Antonio Lanzavecchia
Jens Geginat
Charité - Universitätsmedizin Berlin · DEIstituto Nazionale Genetica Molecolare · ITGerman Rheumatism Research Centre · DETechnical University of Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-10 produced by regulatory T cell subsets is important for the prevention of autoimmunity and immunopathology, but little is known about the phenotype and function of IL-10-producing memory T cells. Human CD4(+)CCR6(+) memory T cells contained comparable numbers of IL-17- and IL-10-producing cells, and CCR6 was induced under both Th17-promoting conditions and upon tolerogenic T cell priming with transforming growth factor (TGF)-beta. In normal human spleens, the majority of CCR6(+) memory T cells were in the close vicinity of CCR6(+) myeloid dendritic cells (mDCs), and strikingly, some of them were secreting IL-10 in situ. Furthermore, CCR6(+) memory T cells produced suppressive IL-10 but not IL-2 upon stimulation with autologous immature mDCs ex vivo, and secreted IL-10 efficiently in response to suboptimal T cell receptor (TCR) stimulation with anti-CD3 antibodies. However, optimal TCR stimulation of CCR6(+) T cells induced expression of IL-2, interferon-gamma, CCL20, and CD40L, and autoreactive CCR6(+) T cell lines responded to various recall antigens. Notably, we isolated autoreactive CCR6(+) T cell clones with context-dependent behavior that produced IL-10 with autologous mDCs alone, but that secreted IL-2 and proliferated upon stimulation with tetanus toxoid. We propose the novel concept that a population of memory T cells, which is fully equipped to participate in secondary immune responses upon recognition of a relevant recall antigen, contributes to the maintenance of tolerance under steady-state conditions.

Indexed as

Immunologic MemoryCD4-Positive T-LymphocytesGene Expression RegulationHomeostasisHumansImmunosuppression TherapyInterferon-gammaInterleukin-10Interleukin-2Receptors, Antigen, T-CellReceptors, CCR6T-LymphocytesT-Lymphocytes, RegulatoryTransforming Growth Factor betaCCR6 protein, humanInterferon-gammaInterleukin-10Interleukin-2Receptors, Antigen, T-CellReceptors, CCR6Transforming Growth Factor beta

Identifiers

PMID20194631
PMCPMC2839148
OpenAlexW2157480023

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.