Evidence map›Paper›PMID 25152867›Full record

ReviewFrontiers in oncology2014

Utilizing regulatory T cells against rheumatoid arthritis.

Mohammad Haque, Kristin Fino, Fengyang Lei, Xiaofang Xiong, Jianxun Song

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Bone Morphogenetic Proteins Shape TFrontiers in immunology · 2022
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Targeting the epitope spreader Pep19 by naïve human CD45RAJournal of periodontal & implant science · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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

5 authors at 1 institution in 1 country.

Mohammad HaqueDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine , Hershey, PA , USA.
Kristin FinoDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine , Hershey, PA , USA.
Fengyang LeiDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine , Hershey, PA , USA.
Xiaofang XiongDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine , Hershey, PA , USA.
Jianxun SongDepartment of Microbiology and Immunology, Pennsylvania State University College of Medicine , Hershey, PA , USA.
Pennsylvania State University · US

Funding

Directed differentiation of HBV-specific CTL from iPSC for cell-based therapiesR21AI109239 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SONG, JIANXUN JIM · 2014 to 2015
$441k
Impact of Highly Active T Lymphocytes from Induced Pluripotent Stem CellsK18CA151798 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI SONG, JIANXUN JIM · 2011 to 2012
$234k
NCI NIH HHS K18 CA151798NIAID NIH HHS R21 AI109239
6 · The paper itself

Abstract

Regulatory T (Treg) cells are essential for normal immune surveillance systems, and their dysfunction leads to development of diseases, such as autoimmune disorders. CD4(+)CD25(+) Treg cells are well-known suppressive cells, which express the transcription factor Foxp3, are indispensable for the maintenance of immune self-tolerance and homeostasis by suppressing aberrant or excessive immune response. Other Foxp3(-) Treg cells include Tr1, Th3, CD8(+)CD28(-/-), and Qa1-restricted T cells; however, the contribution of these Treg cells to self-tolerance, immune homeostasis as well as preventing autoimmunity is not well defined. Here, we discuss the phenotypes and function of Foxp3(+) Treg cells and the potential use of such Treg cells against rheumatoid arthritis (RA). Of note, even though most expanded populations of Foxp3(+) Treg cells exhibit suppressive activity, tissue-associated or antigen-specific Treg cells appear superior in suppressing local autoimmune disorders such as RA. In addition, utilizing tissue-associated Foxp3(+) Treg cells from stem cells may stable Foxp3 expression and avoid induction of a potentially detrimental systemic immunosuppression.

Indexed as

autoimmunitycell-based therapiesregulatory T cellsrheumatoid arthritisstem cellssuppressive cytokines

Identifiers

PMID25152867
PMCPMC4125784
OpenAlexW2147579309

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.