Evidence map›Paper›PMID 26193065›Full record

ReviewTransplantation2015

Advances on Non-CD4 + Foxp3+ T Regulatory Cells: CD8+, Type 1, and Double Negative T Regulatory Cells in Organ Transplantation.

Ann J Ligocki, Jerry Y Niederkorn

Abstract readReview
In one paragraph

Review in Transplantation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-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

27 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Human CD36Immunology · 2021
    Article
  8. Article
  9. Coexpression of Helios in Foxp3Disease markers · 2021
    Review
  10. The Blockade of Interleukin-2 During the Acute Phase ofFrontiers in cellular and infection microbiology · 2021
    Article
  11. New Insights on CD8Frontiers in immunology · 2021
    Review
  12. Microbiota-host interactions shape ageing dynamics.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Commensal Bacteria-Specific CD4Frontiers in immunology · 2018
    Review
  19. Review
  20. Review
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

2 authors at 1 institution in 1 country.

Ann J Ligocki1 Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX.
Jerry Y Niederkorn
The University of Texas Southwestern Medical Center · US

Funding

TRANSPLANT AND TUMOR REJECTION PROCESSES WITHIN THE EYER01EY005631 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI NIEDERKORN, JERRY · 1985 to 2015
$5.8M
THE IMMUNOBIOLOGY OF CORNEAL ALLOGRAFTSR01EY007641 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI NIEDERKORN, JERRY · 1988 to 2016
$5.6M
Core Grant for Vision ResearchP30EY020799 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI NIEDERKORN, JERRY · 2010 to 2016
$4.1M
INFRASTRUCTIRE DEVELOPMENT GRANT FOR CORNEA RESEARCHR24EY016664 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI NIEDERKORN, JERRY · 2005 to 2009
$1.2M
NEI NIH HHS EY005631NEI NIH HHS EY007641NEI NIH HHS EY020799NEI NIH HHS P30 EY020799NEI NIH HHS R01 EY005631NEI NIH HHS R01 EY007641NEI NIH HHS R24 EY016664
6 · The paper itself

Abstract

The overwhelming body of research on T regulatory cells (Treg) has focused on CD4 + CD25 + Foxp3+ T cells. However, recent years have witnessed a resurgence in interest in CD4 - CD8+, CD4 - CD8- (double negative [DN]), and CD4 + Foxp3- type 1 Treg (Tr1) Treg and their role in controlling autoimmune diseases and in promoting the survival of organ allografts and xenografts. CD8+ and DN Treg can arise spontaneously (natural Treg) or can be induced in situ. Both CD8+ and DN Treg have been shown to enhance the survival of organ allografts and xenografts. Additionally, both can suppress alloimmune responses by contact-dependent mechanisms by either inducing apoptosis or mediating direct cytolysis of effector T cells. CD8+, DN, and Tr1 Treg can also act in a contact-independent manner by elaborating soluble immunosuppressive factors, such as TGF-β and IL-10. Applying CD8+, DN, and Tr1 Treg for enhancing the survival of organ allografts and xenografts is still in its infancy but holds significant potential. Furthermore, there is a need for a more comprehensive understanding of how current immunosuppressive therapies applied to organ transplantations affect the wide array of Treg populations.

Indexed as

Organ TransplantationTransplantation ToleranceAnimalsBiomarkersCD8-Positive T-LymphocytesGraft RejectionGraft SurvivalHumansImmunosuppressive AgentsPhenotypeSignal TransductionT-Lymphocytes, RegulatoryTreatment OutcomeBiomarkersImmunosuppressive Agents

Identifiers

PMID26193065
PMCPMC4551577
OpenAlexW996613263

What OpenQuestion holds

Textmetadata
LicenceTDM
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.