Evidence map›Paper›PMID 27869818›Full record

ArticleNature immunology2017

TCRα-TCRβ pairing controls recognition of CD1d and directs the development of adipose NKT cells.

Joshua A Vieth, Joy Das, Fanomezana M Ranaivoson, Davide Comoletti, Lisa K Denzin, Derek B Sant'Angelo

Erratum issuedAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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  20. Are fat NKT cells born that way?Cellular & molecular immunology · 2017
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Joshua A ViethChild Health Institute of New Jersey, Rutgers University, New Brunswick, New Jersey, USA.
Joy DasImmunology Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
Fanomezana M RanaivosonChild Health Institute of New Jersey, Rutgers University, New Brunswick, New Jersey, USA.
Davide ComolettiChild Health Institute of New Jersey, Rutgers University, New Brunswick, New Jersey, USA.
Lisa K DenzinChild Health Institute of New Jersey, Rutgers University, New Brunswick, New Jersey, USA.
Derek B Sant'AngeloChild Health Institute of New Jersey, Rutgers University, New Brunswick, New Jersey, USA.
Rutgers, The State University of New Jersey · USJohnson University · USMemorial Sloan Kettering Cancer Center · US

Funding

Immunobiology of NKT cell development and functionR01AI059739 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI SANT'ANGELO, DEREK B. · 2006 to 2010
$2.5M
The function of PLZF in innate T cellsR01AI083988 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI SANT'ANGELO, DEREK B. · 2010 to 2014
$2.2M
Caspr2 as an autism candidate gene: a proteomic approach to function & structure.R01MH092906 · NIMH · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI COMOLETTI, DAVIDE · 2011 to 2015
$1.6M
Characterization of a novel ILC-like population of adipose-resident cellsR21AI138505 · NIAID · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI SANT'ANGELO, DEREK B. · 2019 to 2020
$437k
PLZF expression in adipose resident natural killer T cellsR21AI159066 · NIAID · RBHS-ROBERT WOOD JOHNSON MEDICAL SCHOOL · PI SANT'ANGELO, DEREK B. · 2021 to 2022
$431k
NIAID NIH HHS R01 AI059739NIAID NIH HHS R01 AI083988NIAID NIH HHS R21 AI138505NIAID NIH HHS R21 AI159066NIMH NIH HHS R01 MH092906
6 · The paper itself

Abstract

The interaction between the T cell antigen receptor (TCR) expressed by natural killer T cells (NKT cells) and the antigen-presenting molecule CD1d is distinct from interactions between the TCR and major histocompatibility complex (MHC). Our molecular modeling suggested that a hydrophobic patch created after TCRα-TCRβ pairing has a role in maintaining the conformation of the NKT cell TCR. Disruption of this patch ablated recognition of CD1d by the NKT cell TCR but not interactions of the TCR with MHC. Partial disruption of the patch, while permissive to the recognition of CD1d, significantly altered NKT cell development, which resulted in the selective accumulation of adipose-tissue-resident NKT cells. These results indicate that a key component of the TCR is essential for the development of a distinct population of NKT cells.

Indexed as

Adipose TissueAnimalsAntigen PresentationAntigens, CD1dCell DifferentiationCells, CulturedComputer SimulationHistocompatibility Antigens Class IMiceMice, Inbred C57BLMice, TransgenicNatural Killer T-CellsProtein BindingProtein ConformationProtein EngineeringProtein MultimerizationAntigens, CD1dHistocompatibility Antigens Class IReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID27869818
OpenAlexW2550443214

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.