Evidence map›Paper›PMID 20146065›Full record

ReviewSeminars in immunopathology2010

SLAM family receptors and the SLAM-associated protein (SAP) modulate T cell functions.

Cynthia Detre, Marton Keszei, Xavier Romero, George C Tsokos, Cox Terhorst

Abstract readReview
In one paragraph

Review in Seminars in immunopathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

75 citing papers in PubMed, 126 citations in OpenAlex.

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15 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

5 authors at 3 institutions in 1 country.

Cynthia DetreBIDMC Division of Immunology, Harvard Center for Life Sciences, Rm. CLS 938, 3 Blackfan Circle, Boston, MA 02115, USA. cdetre@bidmc.harvard.edu
Marton Keszei
Xavier Romero
George C Tsokos
Cox Terhorst
Beth Israel Deaconess Medical Center · USBeth Israel Deaconess Hospital · USHarvard University · US

Funding

The Slamf3, Slamf5, and Slamf6 receptor-induced pathways to murine lupusP01AI065687 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 2006 to 2016
$14.7M
TRANSGENIC MODELS OF T CELL RECEPTOR IMMUNODEFICIENCIESP01AI035714 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 1994 to 2007
$9.3M
Role of TACI mutations in CVIDP01AI076210 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 2009 to 2013
$9.0M
Cell Surface Receptors on T Cells and MacrophagesR01AI015066 · NIAID · DANA-FARBER CANCER INSTITUTE · PI TERHORST, CORNELIS P · 1985 to 2011
$4.7M
Study of LY108 innate and adaptive immune responsesR01DK073339 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TERHORST, CORNELIS P · 2006 to 2013
$2.4M
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-065687NIAID NIH HHS AI-076210NIAID NIH HHS AI-15066NIAID NIH HHS P01 AI035714NIAID NIH HHS P01 AI065687NIAID NIH HHS P01 AI076210NIAID NIH HHS R01 AI015066NIAID NIH HHS R56 AI015066NIDDK NIH HHS R01 DK073339
6 · The paper itself

Abstract

One or more of the signaling lymphocytic activation molecule (SLAM) family (SLAMF) of cell surface receptors, which consists of nine transmembrane proteins, i.e., SLAMF1-9, are expressed on most hematopoietic cells. While most SLAMF receptors serve as self-ligands, SLAMF2 and SLAMF4 use each other as counter structures. Six of the receptors carry one or more copies of a unique intracellular tyrosine-based switch motif, which has high affinity for the single SH2-domain signaling molecules SLAM-associated protein and EAT-2. Whereas SLAMF receptors are costimulatory molecules on the surface of CD4+, CD8+, and natural killer (NK) T cells, they also involved in early phases of lineage commitment during hematopoiesis. SLAMF receptors regulate T lymphocyte development and function and modulate lytic activity, cytokine production, and major histocompatibility complex-independent cell inhibition of NK cells. Furthermore, they modulate B cell activation and memory generation, neutrophil, dendritic cell, macrophage and eosinophil function, and platelet aggregation. In this review, we will discuss the role of SLAM receptors and their adapters in T cell function, and we will examine the role of these receptors and their adapters in X-linked lymphoproliferative disease and their contribution to disease susceptibility in systemic lupus erythematosus.

Indexed as

AnimalsAntigens, CDCell DifferentiationGenetic Predisposition to DiseaseHumansIntracellular Signaling Peptides and ProteinsLupus Erythematosus, SystemicLymphocyte ActivationLymphoproliferative DisordersReceptors, Cell SurfaceSignaling Lymphocytic Activation Molecule Associated ProteinSignaling Lymphocytic Activation Molecule Family Member 1T-LymphocytesAntigens, CDIntracellular Signaling Peptides and ProteinsReceptors, Cell SurfaceSH2D1A protein, humanSignaling Lymphocytic Activation Molecule Associated ProteinSignaling Lymphocytic Activation Molecule Family Member 1SLAMF1 protein, human

Identifiers

PMID20146065
PMCPMC2868096
OpenAlexW2017213329

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.