Evidence map›Paper›PMID 24082012›Full record

ArticleJournal of leukocyte biology2014

Differential role of all-trans retinoic acid in promoting the development of CD4+ and CD8+ regulatory T cells.

Jilin Ma, Ya Liu, Yang Li, Jian Gu, Justin Liu, Jiayou Tang, Julie Wang, Bernhard Ryffel, Yi Shen, David Brand and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. CD8Rheumatology and immunology research · 2021
    Review
  8. Review
  9. Tregs in Autoimmune Uveitis.Advances in experimental medicine and biology · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Role of Vitamin A in the Immune System.Journal of clinical medicine · 2018
    Review
  14. Review
  15. TGF-β-Induced CD8Frontiers in immunology · 2018
    Article
  16. Epigenetic involvement in etiopathogenesis and implications in treatment of systemic lupus erythematous.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  17. Review
  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

12 authors at 4 institutions in 3 countries.

Jilin Ma2.Penn State University Hershey College of Medicine, 500 University Drive, Hershey, PA 17033. szheng1@hmc.psu.edu; Division of Rheumatology, Immunology and Nephrology, Zhejiang Traditional Chinese Medicine and Western Medicine Hospital, 208 Huancheng East Road, Hangzhou 310003, P. R. China. E-mail: majilin0808@sohu.com.
Ya Liu
Yang Li
Jian Gu
Justin Liu
Jiayou Tang
Julie Wang
Bernhard Ryffel
Yi Shen
David Brand
Zhongmin Liu
Song Guo Zheng
Shanghai East Hospital · CNUniversity of Southern California · USUniversité d'Orléans · FRUniversity of California, San Diego · US

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
Generation of Regulatory T cells ex-vivo for the treatment of systemic lupus erytR43AI084359 · NIAID · EXCELL THERAPEUTICS, LLC · PI O'NEIL, DAVID · 2011 to 2011
$245k
NIAID NIH HHS AI084359NIAID NIH HHS R43 AI084359NIAMS NIH HHS AR059103NIAMS NIH HHS R01 AR059103
6 · The paper itself

Abstract

It is known that ATRA promotes the development of TGF-β-induced CD4(+)Foxp3(+) iTregs, which play a vital role in the prevention of autoimmune diseases; however, the role of ATRA in facilitating the differentiation and function of CD8(+)Foxp3(+) iTregs remains elusive. Using a head-to-head comparison, we found that ATRA promoted expression of Foxp3 and development of CD4(+) iTregs, but it did not promote Foxp3 expression on CD8(+) cells. Using a standard in vitro assay, we demonstrated that CD8(+) iTregs induced by TGF-β and ATRA were not superior to CD8(+) iTregs induced by TGF-β alone. In cGVHD, in a typical lupus syndrome model where DBA2 spleen cells were transferred to DBA2xC57BL/6 F1 mice, we observed that both CD8(+) iTregs induced by TGF-β and ATRA and those induced by TGF-β alone had similar therapeutic effects. ATRA did not boost but, conversely, impaired the differentiation and function of human CD8(+) iTregs. CD8(+) cells expressed the ATRA receptor RAR and responded to ATRA, similar to CD4(+) cells. We have identified the differential role of ATRA in promoting Foxp3(+) Tregs in CD4(+) and CD8(+) cell populations. These results will help to determine a protocol for developing different Treg cell populations and may provide novel insights into clinical cell therapy for patients with autoimmune diseases and those needing organ transplantation.

Indexed as

AnimalsCD8-Positive T-LymphocytesFemaleForkhead Transcription FactorsHumansImmune ToleranceLymphocyte ActivationMaleMiceT-Lymphocytes, RegulatoryTransforming Growth Factor betaTretinoinForkhead Transcription FactorsFoxp3 protein, mouseTransforming Growth Factor betaTretinoinall-trans retinoic acidAutoimmunityFoxp3GVHDregulatory T cellsTGF-β

Identifiers

PMID24082012
PMCPMC3896662
OpenAlexW2109402444

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.