Evidence map›Paper›PMID 17509909›Full record

ArticleImmunity2007

Regulation of activated CD4+ T cells by NK cells via the Qa-1-NKG2A inhibitory pathway.

Linrong Lu, Koichi Ikizawa, Dan Hu, Miriam B F Werneck, Kai W Wucherpfennig, Harvey Cantor

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
137citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

137 citing papers in PubMed, 1 synthesis or guideline pooled it, 245 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Unconventional functions of natural killer cells in homeostasis and disease.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Review
  8. Article
  9. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  10. Cytotoxic T Cells: Kill, Memorize, and Mask to Maintain Immune Homeostasis.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Generation of an Inhibitory NK Cell Subset by TGF-β1/IL-15 Polarization.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  19. Article
  20. Review

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

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

6 authors at 2 institutions in 1 country.

Linrong LuDepartment of Cancer Immunology & AIDS, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Koichi Ikizawa
Dan Hu
Miriam B F Werneck
Kai W Wucherpfennig
Harvey Cantor
Harvard University · USDana-Farber Cancer Institute · US

Funding

IMMUNOLOGIC MECHANISMS THAT PREVENT AUTOIMMUNITYR01AI037562 · NIAID · DANA-FARBER CANCER INSTITUTE · PI CANTOR, HARVEY · 1996 to 2021
$9.4M
NIAID NIH HHS AI 37562NIAID NIH HHS R01 AI037562
6 · The paper itself

Abstract

The ability of natural-killer cells to regulate adaptive immunity is not well understood. Here we define an interaction between the class Ib major histocompatibility complex (MHC) molecule Qa-1-Qdm on activated T cells responsible for adaptive immunity and CD94-NKG2A inhibitory receptors expressed by natural-killer cells by using Qa-1-deficient and Qa-1 knockin mice containing a point mutation that selectively abolishes Qa-1-Qdm binding to CD94-NKG2A receptors. The Qa-1-NKG2A interaction protected activated CD4+ T cells from lysis by a subset of NKG2A+ NK cells and was essential for T cell expansion and development of immunologic memory. Antibody-dependent blockade of this Qa-1-NKG2A interaction resulted in potent NK-dependent elimination of activated autoreactive T cells and amelioration of experimental autoimmune encephalomyelitis. These findings extend the functional reach of the NK system to include regulation of adaptive T cell responses and suggest a new clinical strategy for elimination of antigen-activated T cells in the context of autoimmune disease and transplantation.

Indexed as

AnimalsBone MarrowCD4-Positive T-LymphocytesCell ProliferationCells, CulturedChimerin ProteinsDNA-Binding ProteinsEncephalomyelitis, Autoimmune, ExperimentalGene Expression RegulationGenetic Predisposition to DiseaseHistocompatibility Antigens Class IImmunologic MemoryInterferon-gammaKiller Cells, NaturalLentivirusLymphocyte ActivationChimerin ProteinsDNA-Binding ProteinsHistocompatibility Antigens Class IInterferon-gammaKlrc1 protein, mouseNK Cell Lectin-Like Receptor Subfamily CNK Cell Lectin-Like Receptor Subfamily DQ surface antigensRag2 protein, mouseReceptors, ImmunologicReceptors, Natural Killer Cell

Identifiers

PMID17509909
PMCPMC3428267
OpenAlexW2049238953

What OpenQuestion holds

Textmetadata
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.