Evidence map›Paper›PMID 25376021›Full record

ArticlePLoS computational biology2014

Relationships between Th1 or Th2 iNKT cell activity and structures of CD1d-antigen complexes: meta-analysis of CD1d-glycolipids dynamics simulations.

Xavier Laurent, Nicolas Renault, Amaury Farce, Philippe Chavatte, Eric Hénon

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 5 institutions in 1 country.

Xavier LaurentIntestinal Biotech Development, Faculté de Médecine, Lille, France; Laboratoire de Chimie Thérapeutique EA4481, Université Lille 2, Lille, France.
Nicolas RenaultLaboratoire de Chimie Thérapeutique EA4481, Université Lille 2, Lille, France.
Amaury FarceLaboratoire de Chimie Thérapeutique EA4481, Université Lille 2, Lille, France.
Philippe ChavatteLaboratoire de Chimie Thérapeutique EA4481, Université Lille 2, Lille, France; Institut de Chimie Pharmaceutique Albert Lespagnol EA4481, Université Lille 2, Lille, France.
Eric HénonInstitut de Chimie Moléculaire de Reims UMR CNRS 7312, University of Reims Champagne-Ardenne, Reims, France.
Centre National de la Recherche Scientifique · FRInstitut de Chimie · FRLaboratoire de Chimie · FRParis Biotech Santé · FRUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of potentially bioactive molecules can be found in nature. In particular, marine organisms are a valuable source of bioactive compounds. The activity of an α-galactosylceramide was first discovered in 1993 via screening of a Japanese marine sponge (Agelas mauritanius). Very rapidly, a synthetic glycololipid analogue of this natural molecule was discovered, called KRN7000. Associated with the CD1d protein, this α-galactosylceramide 1 (KRN7000) interacts with the T-cell antigen receptor to form a ternary complex that yields T helper (Th) 1 and Th2 responses with opposing effects. In our work, we carried out molecular dynamics simulations (11.5 µs in total) involving eight different ligands (conducted in triplicate) in an effort to find out correlation at the molecular level, if any, between chemical modulation of 1 and the orientation of the known biological response, Th1 or Th2. Comparative investigations of human versus mouse and Th1 versus Th2 data have been carried out. A large set of analysis tools was employed including free energy landscapes. One major result is the identification of a specific conformational state of the sugar polar head, which could be correlated, in the present study, to the biological Th2 biased response. These theoretical tools provide a structural basis for predicting the very different dynamical behaviors of α-glycosphingolipids in CD1d and might aid in the future design of new analogues of 1.

Indexed as

AnimalsAntigens, CD1dGlycolipidsHumansMiceMolecular Dynamics SimulationNatural Killer T-CellsTh1 CellsTh2 CellsThermodynamicsAntigens, CD1dGlycolipids

Identifiers

PMID25376021
PMCPMC4222593
OpenAlexW2049774707

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.