Evidence map›Paper›PMID 21257291›Full record

ArticleJournal of autoimmunity2011

Neuroantigen-specific CD8+ regulatory T-cell function is deficient during acute exacerbation of multiple sclerosis.

Ethan J Baughman, Jason P Mendoza, Sterling B Ortega, Chris L Ayers, Benjamin M Greenberg, Elliot M Frohman, Nitin J Karandikar

Abstract read
In one paragraph

Article in Journal of autoimmunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

55 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. CD4European journal of immunology · 2026
    Article
  3. Myelin-reactive CD8Journal of neuroinflammation · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Increased Percentage of CD8Neurology(R) neuroimmunology & neuroinflammation · 2023
    Article
  9. Article
  10. The immunology of multiple sclerosis.Nature reviews. Immunology · 2022
    Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. CD8Cell death & disease · 2021
    Article
  18. Review
  19. A Functionally Distinct CXCR3Journal of immunology (Baltimore, Md. : 1950) · 2021
    Article
  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

7 authors at 3 institutions in 1 country.

Ethan J BaughmanDepartment of Pathology, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.
Jason P Mendoza
Sterling B Ortega
Chris L Ayers
Benjamin M Greenberg
Elliot M Frohman
Nitin J Karandikar
Southwestern Medical CenterThe University of Texas Southwestern Medical Center · USSouthwestern Medical Center · US

Funding

T CELLS IN THE IMMUNOMODULATION OF MSR01AI053439 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2003 to 2011
$3.2M
AUTOREACTIVE CD8+ T CELLS IN MULTIPLE SCLEROSISR01AI065463 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2007 to 2010
$1.4M
DISSECTING THE IMMUNE BASIS OF DISEASE AND THERAPYK24AI079272 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2009 to 2013
$1.1M
ROLE OF T CELLS IN THE IMMUNOMODULATION OF MSR56AI053439 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2007 to 2007
$314k
AUTOREACTIVE CD8+ T CELLS IN MULTIPLE SCLEROSISR56AI065463 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI KARANDIKAR, NITIN J · 2006 to 2006
$314k
NIAID NIH HHS K24 AI079272NIAID NIH HHS R01 AI053439NIAID NIH HHS R01 AI065463NIAID NIH HHS R56 AI053439NIAID NIH HHS R56 AI065463
6 · The paper itself

Abstract

Multiple sclerosis (MS) is an inflammatory, demyelinating disease of the central nervous system (CNS). MS is thought to be T-cell-mediated, with prior research predominantly focusing on CD4+ T-cells. There is a high prevalence of CNS-specific CD8+ T-cell responses in MS patients and healthy subjects. However, the role of neuroantigen-specific CD8+ T-cells in MS is poorly understood, with the prevalent notion that these may represent pathogenic T-cells. We show here that healthy subjects and MS patients demonstrate similar magnitudes of CD8+ and CD4+ T-cell responses to various antigenic stimuli. Interestingly, CD8+ T-cells specific for CNS autoantigens, but not those specific for control foreign antigens, exhibit immune regulatory ability, suppressing proliferation of CD4+CD25- T-cells when stimulated by their cognate antigen. While CD8+ T-cell-mediated immune suppression is similar between healthy subjects and clinically quiescent treatment-naïve MS patients, it is significantly deficient during acute exacerbation of MS. Of note, the recovery of neuroantigen-specific CD8+ T-cell suppression correlates with disease recovery post-relapse. These studies reveal a novel immune suppressor function for neuroantigen-specific CD8+ T-cells that is clinically relevant in the maintenance of peripheral tolerance and the intrinsic regulation of MS immune pathology.

Indexed as

AdultAgedAntigensAutoantigensCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell LineCell ProliferationCentral Nervous SystemFemaleFlow CytometryHumansInterleukin-2 Receptor alpha SubunitMaleMiddle AgedMultiple SclerosisAntigensAutoantigensInterleukin-2 Receptor alpha Subunit

Identifiers

PMID21257291
PMCPMC3046327
OpenAlexW1973240867

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.