Evidence map›Paper›PMID 21889557›Full record

ArticleHuman immunology2012

Global expression profiling of peripheral Qa-1-restricted CD8αα+TCRαβ+ regulatory T cells reveals innate-like features: implications for immune-regulatory repertoire.

Shaohsuan S Fanchiang, Radu Cojocaru, Mohammad Othman, Ritu Khanna, Matthew J Brooks, Trevor Smith, Xiaolei Tang, Igor Maricic, Anand Swaroop, Vipin Kumar

Abstract read
In one paragraph

Article in Human immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. CD8ααSkin health and disease · 2021
    Article
  4. Distinct PLZFJournal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  5. Advances in the Study of CD8+ Regulatory T Cells.Critical reviews in immunology · 2019
    Review
  6. Review
  7. Article
  8. Review
  9. 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

10 authors at 4 institutions in 1 country.

Shaohsuan S FanchiangLaboratory of Autoimmunity, Torrey Pines Institute for Molecular Studies, San Diego, California, USA.
Radu Cojocaru
Mohammad Othman
Ritu Khanna
Matthew J Brooks
Trevor Smith
Xiaolei Tang
Igor Maricic
Anand Swaroop
Vipin Kumar
Torrey Pines Institute For Molecular Studies · USNational Institutes of Health · USUniversity of Michigan–Ann Arbor · USNational Eye Institute · US

Funding

Regulation of retinal developmentZIAEY000450 · NEI · NATIONAL EYE INSTITUTE · PI SWAROOP, ANAND · 2009 to 2025
$71.0M
Regulatory CD4/CD8 T cells in autoimmune demyelinationR01AI052227 · NIAID · TORREY PINES INST FOR MOLECULAR STUDIES · PI KUMAR, VIPIN · 2003 to 2006
$1.4M
NIAID NIH HHS R01 AI052227NIAID NIH HHS R01AI05227
6 · The paper itself

Abstract

Among peripheral regulatory T cells, CD8(+) T cells also play an important role in the maintenance of immune homeostasis. A subset of CD8(+) Treg that express αβ T cell receptor (TCR) and CD8αα homodimers can recognize TCR-derived peptides in the context of the class Ib MHC molecule Qa-1. To gain a better understanding of the nature and phenotype of CD8αα(+)TCRαβ+ Treg, a global gene expression profiling using microarray, real-time quantitative polymerase chain reaction, and flow-cytometric analysis was performed using functional Treg clones and lines. The study findings show that CD8(+) Treg shared gene profile expressed by innate-like lymphocytes, including murine intraepithelial lymphocytes and thymic CD8αα(+)TCRαβ+ T-cell populations. In addition, this subset displays differential expression of several key regulatory molecules, including CD200. CD8αα(+) Treg expressed higher levels of a number of natural killer cell-related receptors and molecules belonging to the TNF superfamily. Collectively, peripheral class Ib-reactive CD8αα(+)TCRαβ+ T cells represent a unique regulatory population different from class Ia major histocompatibility complex-restricted conventional T cells. These studies have important implications for the regulatory mechanisms mediated by the CD8(+) Treg population in general.

Indexed as

AnimalsAntigens, CDCD8 AntigensCell LineClone CellsGene Expression ProfilingHistocompatibility Antigens Class IHumansImmunity, InnateImmunomodulationKiller Cells, NaturalMiceMice, TransgenicOligonucleotide Array Sequence AnalysisPeripheral ToleranceProtein BindingAntigens, CDantigens, CD200CD8 antigen, alpha chainCD8 AntigensHistocompatibility Antigens Class IQ surface antigensReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID21889557
PMCPMC3261310
OpenAlexW2066935464

What OpenQuestion holds

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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.