Evidence map›Paper›PMID 20844537›Full record

ArticleNature2010

Inhibition of follicular T-helper cells by CD8(+) regulatory T cells is essential for self tolerance.

Hye-Jung Kim, Bert Verbinnen, Xiaolei Tang, Linrong Lu, Harvey Cantor

Abstract read
In one paragraph

Article in Nature, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 210 papers.

0numbers the graph read from it
0cells of the map it votes in
210citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

210 citing papers in PubMed, 342 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Review
  7. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Regulatory KIRScience translational medicine · 2025
    Article
  17. Article
  18. Distinct functions of CD4Nature immunology · 2025
    Article
  19. Differential roles of human CD4Nature immunology · 2025
    Article
  20. GzmkFrontiers in immunology · 2025
    Review

150 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 2 countries.

Hye-Jung KimDepartment of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115, USA.
Bert Verbinnen
Xiaolei Tang
Linrong Lu
Harvey Cantor
Dana-Farber Cancer Institute · USHarvard University · USZhejiang University · CN

Funding

IMMUNOLOGIC MECHANISMS THAT PREVENT AUTOIMMUNITYR01AI037562 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1996 to 2021
$9.4M
Pathobiology of Cancer at the Host and Population LevelT32CA009382 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI YUAN, ZHI-MIN · 1985 to 2012
$2.9M
Postdoctoral Training Program in Cancer ImmunologyT32CA070083 · NCI · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1997 to 2012
$2.8M
NCI NIH HHS T32 CA009382NCI NIH HHS T32 CA070083NIAID NIH HHS AI 037562NIAID NIH HHS R01 AI037562
6 · The paper itself

Abstract

The ability to produce vigorous immune responses that spare self tissues and organs depends on the elimination of autoreactive T and B cells. However, purging of immature and mature self-reactive T and B cells is incomplete and may also require the involvement of cells programmed to suppress immune responses. Regulatory T cells (T(reg)) belonging to the CD4(+) T-cell subset may have a role in preventing untoward inflammatory responses, but T-cell subsets programmed to inhibit the development of autoantibody formation and systemic-lupus-erythematosus-like disease have not yet been defined. Here we delineate a CD8(+) regulatory T-cell lineage that is essential for the maintenance of self tolerance and prevention of murine autoimmune disease. Genetic disruption of the inhibitory interaction between these CD8(+) T cells and their target Qa-1(+) follicular T-helper cells results in the development of a lethal systemic-lupus-erythematosus-like autoimmune disease. These findings define a sublineage of CD8 T cells programmed to suppress rather than activate immunity that represents an essential regulatory element of the immune response and a guarantor of self tolerance.

Indexed as

AnimalsAntibodiesAntibody AffinityAntigensAutoantibodiesCD8-Positive T-LymphocytesCell LineageGerminal CenterHistocompatibility Antigens Class IHyaluronan ReceptorsImmunoglobulin GLupus Erythematosus, SystemicMiceModels, ImmunologicalMutationSelf ToleranceAntibodiesAntigensAutoantibodiesHistocompatibility Antigens Class IHyaluronan ReceptorsImmunoglobulin GQ surface antigens

Identifiers

PMID20844537
PMCPMC3395240
OpenAlexW1972804526

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.