Evidence map›Paper›PMID 15123745›Full record

ArticleThe Journal of experimental medicine2004

The cell surface receptor SLAM controls T cell and macrophage functions.

Ninghai Wang, Abhay Satoskar, William Faubion, Duncan Howie, Susumu Okamoto, Stefan Feske, Charles Gullo, Kareem Clarke, Miriam Rodriguez Sosa, Arlene H Sharpe and 1 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in The Journal of experimental medicine, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
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

83 citing papers in PubMed, 179 citations in OpenAlex.

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  15. Development of αβ T Cells with Innate Functions.Advances in experimental medicine and biology · 2022
    Article
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23 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

11 authors at 3 institutions in 2 countries.

Ninghai WangDivision of Immunology, RE-204, Beth Israel Deaconess Medical Center, Harvard Medical School, 41 Avenue Louis Pasteur, Boston, MA 02215, USA.
Abhay Satoskar
William Faubion
Duncan Howie
Susumu Okamoto
Stefan Feske
Charles Gullo
Kareem Clarke
Miriam Rodriguez Sosa
Arlene H Sharpe
Cox Terhorst
Hadassah Medical Center · ILHarvard University · USBrigham and Women's Hospital · US

Funding

Cell Surface Receptors on T Cells and MacrophagesR01AI015066 · NIAID · DANA-FARBER CANCER INSTITUTE · PI TERHORST, CORNELIS P · 1985 to 2011
$4.7M
Cell Surface Receptors on T Cells and MacrophagesR56AI015066 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 2013 to 2013
$317k
NIAID NIH HHS AI-015066NIAID NIH HHS R01 AI015066NIAID NIH HHS R56 AI015066
6 · The paper itself

Abstract

Signaling lymphocyte activation molecule (SLAM), a glycoprotein expressed on activated lymphocytes and antigen-presenting cells, has been shown to be a coregulator of antigen-driven T cell responses and is one of the two receptors for measles virus. Here we show that T cell receptor-induced interleukin (IL)-4 secretion by SLAM(-/-) CD4(+) cells is down-regulated, whereas interferon gamma production by CD4(+) T cells is only slightly up-regulated. Although SLAM controls production of IL-12, tumor necrosis factor, and nitric oxide in response to lipopolysaccharide (LPS) by macrophages, SLAM does not regulate phagocytosis and responses to peptidoglycan or CpG. Thus, SLAM acts as a coreceptor that regulates signals transduced by the major LPS receptor Toll-like receptor 4 on the surface of mouse macrophages. A defective macrophage function resulted in an inability of SLAM(-/-) C57Bl/6 mice to remove the parasite Leishmania major. We conclude that the coreceptor SLAM plays a central role at the interface of acquired and innate immune responses.

Indexed as

AnimalsAntigens, CDBase SequenceCD4-Positive T-LymphocytesDNA PrimersGlycoproteinsImmunoglobulinsLeishmania majorLeishmaniasis, CutaneousLipopolysaccharidesMacrophages, PeritonealMiceMice, Inbred BALB CMice, Inbred C57BLMice, Mutant StrainsReceptors, Antigen, T-CellAntigens, CDDNA PrimersGlycoproteinsImmunoglobulinsLipopolysaccharidesReceptors, Antigen, T-CellReceptors, Antigen, T-Cell, alpha-betaReceptors, Cell SurfaceRecombinant ProteinsSignaling Lymphocytic Activation Molecule Family Member 1

Identifiers

PMID15123745
PMCPMC2211908
OpenAlexW2136589340

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.