Evidence map›Paper›PMID 19949076›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2010

Mechanisms for glycolipid antigen-driven cytokine polarization by Valpha14i NKT cells.

Barbara A Sullivan, Niranjana A Nagarajan, Gerhard Wingender, Jing Wang, Iain Scott, Moriya Tsuji, Richard W Franck, Steven A Porcelli, Dirk M Zajonc, Mitchell Kronenberg

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
–field-weighted citation impact
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

77 citing papers in PubMed.

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  9. A DesignedAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
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17 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

10 authors.

Barbara A SullivanDivision of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Niranjana A Nagarajan
Gerhard Wingender
Jing Wang
Iain Scott
Moriya Tsuji
Richard W Franck
Steven A Porcelli
Dirk M Zajonc
Mitchell Kronenberg

Funding

Precision Targeting of CD1-Restricted iNKT Cells for Cancer ImmunotherapyR01AI045889 · NIAID · YESHIVA UNIVERSITY · PI Steven A Porcelli · 1999 to 2026
$9.3M
Development and Function of NKT CellsR37AI071922 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2006 to 2015
$4.9M
Recognition of bacterial antigens by NKT cellsR01AI045053 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI KRONENBERG, MITCHELL · 2000 to 2010
$3.3M
Structural Immunology of CD1 and CD1-TCR ComplexesR01AI074952 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI ZAJONC, DIRK M · 2009 to 2013
$1.8M
Structural Immunology of CD1 and CD1-TCR ComplexesR56AI074952 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI ZAJONC, DIRK M · 2008 to 2008
$412k
Altered Glycolipid Ligands for Va14i NKT cellsF32AI062015 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI SULLIVAN, BARBARA A · 2004 to 2006
$142k
NIAID NIH HHS F32 AI062015NIAID NIH HHS F32 AI62015NIAID NIH HHS R01 AI045053NIAID NIH HHS R01 AI045889NIAID NIH HHS R01 AI074952NIAID NIH HHS R01 AI45053NIAID NIH HHS R01AI45889NIAID NIH HHS R37 AI071922NIAID NIH HHS R37 AI71922NIAID NIH HHS R56 AI074952NIAID NIH HHS R56/R01 AI074952
6 · The paper itself

Abstract

Certain glycolipid Ags for Valpha14i NKT cells can direct the overall cytokine balance of the immune response. Th2-biasing OCH has a lower TCR avidity than the most potent agonist known, alpha-galactosylceramide. Although the CD1d-exposed portions of OCH and alpha-galactosylceramide are identical, structural analysis indicates that there are subtle CD1d conformational differences due to differences in the buried lipid portion of these two Ags, likely accounting for the difference in antigenic potency. Th1-biasing C-glycoside/CD1d has even weaker TCR interactions than OCH/CD1d. Despite this, C-glycoside caused a greater downstream activation of NK cells to produce IFN-gamma, accounting for its promotion of Th1 responses. We found that this difference correlated with the finding that C-glycoside/CD1d complexes survive much longer in vivo. Therefore, we suggest that the pharmacokinetic properties of glycolipids are a major determinant of cytokine skewing, suggesting a pathway for designing therapeutic glycolipids for modulating invariant NKT cell responses.

Indexed as

AnimalsAntigen PresentationAntigensAntigens, CD1dCytokinesFlow CytometryGalactosylceramidesGlycolipidsGlycosidesLymphocyte ActivationMiceMice, Inbred C57BLMonosaccharidesNatural Killer T-CellsSignal TransductionSurface Plasmon Resonancealpha-galactosylceramideAntigensAntigens, CD1dC-glycosideCytokinesGalactosylceramidesGlycolipidsGlycosidesMonosaccharidestetracosanoic acid 1-galactopyranosyloxy-3,4-dihydroxydec-2-yl amide

Identifiers

PMID19949076
PMCPMC2834884

What OpenQuestion holds

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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.