Evidence map›Paper›PMID 11877485›Full record

ArticleThe Journal of experimental medicine2002

Functionally distinct subsets of CD1d-restricted natural killer T cells revealed by CD1d tetramer staining.

Jenny E Gumperz, Sachiko Miyake, Takashi Yamamura, Michael B Brenner

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 346 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
346citing papers in PubMed, 1 pooled it
11.7field-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

346 citing papers in PubMed, 1 synthesis or guideline pooled it, 763 citations in OpenAlex.

  1. Pooled it
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  13. Human CD4Frontiers in immunology · 2026
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286 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

4 authors at 3 institutions in 2 countries.

Jenny E GumperzDivision of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, One Jimmy Fund Way, Boston, MA 02115, USA.
Sachiko Miyake
Takashi Yamamura
Michael B Brenner
National Center of Neurology and Psychiatry · JPBrigham and Women's Hospital · USHarvard University · US

Funding

IMMUNOLOGIC BASIS OF RESISTANCE AND HYPERSENSITIVITYT32AI007306 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI Nora Amanda Barrett, Joshua A Boyce · 1985 to 2026
$12.2M
T LYMPOHOCYTE RECOGNITIONR01AI028973 · NIAID · DANA-FARBER CANCER INSTITUTE · PI BRENNER, MICHAEL B. · 1990 to 2014
$4.5M
T LYMPHOCYTE RECOGNITIONR37AI028973 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B · 1995 to 2004
$1.7M
NIAID NIH HHS AI28973NIAID NIH HHS R01 AI028973NIAID NIH HHS R37 AI028973NIAID NIH HHS T32 AI007306NIAID NIH HHS T32-AI07306
6 · The paper itself

Abstract

CD1d-restricted natural killer (NK)T cells are known to potently secrete T helper (Th)1 and Th2 cytokines and to mediate cytolysis, but it is unclear how these contrasting functional activities are regulated. Using lipid antigen-loaded CD1d tetramers, we have distinguished two subsets of CD1d-restricted T cells in fresh peripheral blood that differ in cytokine production and cytotoxic activation. One subset, which was CD4(-), selectively produced the Th1 cytokines interferon gamma and tumor necrosis factor alpha, and expressed NKG2d, a marker associated with cytolysis of microbially infected and neoplastic cells. This subset up-regulated perforin after exposure to interleukin (IL)-2 or IL-12. In contrast, CD4(+) CD1d-restricted NKT cells potently produced both Th1 and Th2 cytokines, up-regulated perforin in response to stimulation by phorbol myristate acetate and ionomycin but not IL-2 or IL-12, and could be induced to express CD95L. Further, for both CD1d-restricted NKT cell subsets, we found that antigenic stimulation induced cytokine production but not perforin expression, whereas exposure to inflammatory factors enhanced perforin expression but did not stimulate cytokine production. These results show that the various activities of CD1d-restricted T cells in tumor rejection, autoimmune disease, and microbial infections could result from activation of functionally distinct subsets, and that inflammatory and antigenic stimuli may influence different effector functions.

Indexed as

Lectins, C-TypeAnimalsAntigens, CD1Antigens, CD1dAntigens, SurfaceCytokinesCytotoxicity, ImmunologicGalactosylceramidesHumansKiller Cells, NaturalMiceNK Cell Lectin-Like Receptor Subfamily BNK Cell Lectin-Like Receptor Subfamily KReceptors, ImmunologicReceptors, Lymphocyte HomingReceptors, Natural Killer CellAntigens, CD1Antigens, CD1dAntigens, SurfaceCD1D protein, humanCytokinesGalactosylceramidesKLRB1 protein, humanKLRK1 protein, humanKlrk1 protein, mouseLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily BNK Cell Lectin-Like Receptor Subfamily KReceptors, ImmunologicReceptors, Lymphocyte HomingReceptors, Natural Killer Cell

Identifiers

PMID11877485
PMCPMC2193772
OpenAlexW2167094013

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.