Evidence map›Paper›PMID 22605463›Full record

ArticleArthritis and rheumatism2012

Antigen-specific transforming growth factor β-induced Treg cells, but not natural Treg cells, ameliorate autoimmune arthritis in mice by shifting the Th17/Treg cell balance from Th17 predominance to Treg cell predominance.

Ning Kong, Qin Lan, Maogen Chen, Julie Wang, Wei Shi, David A Horwitz, Valerie Quesniaux, Bernhard Ryffel, Zhongmin Liu, David Brand and 2 more

Abstract read
In one paragraph

Article in Arthritis and rheumatism, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
–field-weighted citation impact
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

79 citing papers in PubMed.

  1. Article
  2. TGF-β signaling mediates crosstalk between CD8Journal of biomedical science · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. IL-17: an important pathogenic factor in endometriosis.International journal of medical sciences · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Tregs in Autoimmune Uveitis.Advances in experimental medicine and biology · 2021
    Article

19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Ning KongUniversity of Southern California, Los Angeles, CA 90033, USA.
Qin Lan
Maogen Chen
Julie Wang
Wei Shi
David A Horwitz
Valerie Quesniaux
Bernhard Ryffel
Zhongmin Liu
David Brand
Hejian Zou
Song Guo Zheng

Funding

Therapeutic immunoregulation mediated by TGF-??-induced iTregs in autoimmune arthR01AR059103 · NIAMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI JARJOUR, WAEL N · 2010 to 2020
$3.9M
NIAMS NIH HHS R01 AR059103NIAMS NIH HHS R01-AR-059103
6 · The paper itself

Abstract

objectiveTransferred CD4+CD25+FoxP3+ Treg cells can prevent autoimmune disease, but generally fail to ameliorate established disease. This study was undertaken to compare the effects of antigen-specific Treg cells induced with interleukin-2 (IL-2) and transforming growth factor β (TGFβ) ex vivo (induced Treg [iTreg] cells) to the effects of equivalent expanded thymus-derived natural Treg (nTreg) cells on established collagen-induced arthritis (CIA).

methodsCIA was induced in DBA/1 mice by immunization with type II collagen (CII), and before or shortly after immunization, mice were treated with iTreg or nTreg cells that were generated or expanded in vitro. Clinical scores were determined. Inflammatory responses were determined by measuring the levels of anti-CII antibody in the serum and examining the histologic features of the mouse joints. The Th1/Th17-mediated autoreactive response was evaluated by determining the cytokine profile of the draining lymph node (LN) cells of the mice by flow cytometry.

resultsFollowing transfer, nTreg cells exhibited decreased FoxP3 and Bcl-2 expression and decreased suppressive activity, and many converted to Th17 cells. In contrast, transferred iTreg cells were more numerous, retained FoxP3 expression and their suppressive activity in the presence of IL-6, and were resistant to Th17 conversion. Notably, 10 days after the transfer of donor iTreg cells, predominance was shifted from Th17 cells to Treg cells in the draining LNs of recipient mice.

conclusionThese findings provide evidence that transferred TGFβ-induced iTreg cells are more stable and functional than nTreg cells in mice with established autoimmunity. Moreover, iTreg cells can have tolerogenic effects even in the presence of ongoing inflammation. The therapeutic potential of human iTreg cells in subjects with chronic, immune-mediated inflammatory diseases should be investigated.

Indexed as

AnimalsArthritis, ExperimentalAutoimmune DiseasesCell CountCell DifferentiationDisease Models, AnimalFemaleForkhead Transcription FactorsMiceMice, Inbred C57BLMice, Inbred DBAProto-Oncogene Proteins c-bcl-2Th17 CellsT-Lymphocytes, RegulatoryTransforming Growth Factor betaForkhead Transcription FactorsFoxp3 protein, mouseProto-Oncogene Proteins c-bcl-2Transforming Growth Factor beta

Identifiers

PMID22605463
PMCPMC4364395

What OpenQuestion holds

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Registered trials

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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.