Evidence map›Paper›PMID 19647320›Full record

ArticleMolecular immunology2009

HLA-DM mediates peptide exchange by interacting transiently and repeatedly with HLA-DR1.

Kedar Narayan, Katherine W Su, Chih-Ling Chou, Stanislav Khoruzhenko, Scheherazade Sadegh-Nasseri

Abstract read
In one paragraph

Article in Molecular immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.6field-weighted citation impact, top 32% 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, 35 citations in OpenAlex.

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  16. Evaluating the Role of HLA-DM in MHC Class II-Peptide Association Reactions.Journal of immunology (Baltimore, Md. : 1950) · 2015
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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 1 institution in 1 country.

Kedar NarayanGraduate Program in Immunology, Johns Hopkins Medical Institutions, Baltimore, MD 21205, USA.
Katherine W Su
Chih-Ling Chou
Stanislav Khoruzhenko
Scheherazade Sadegh-Nasseri
Johns Hopkins University · US

Funding

Role of DM in Generation of Immunodominant Epitope(s)R01AI063764 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SADEGH-NASSERI, SCHEHERAZADE · 2006 to 2015
$3.6M
STRUCTURE/BIOLOGY OF SHORT LIVED MHC II LIGAND COMPLEXESR01GM053549 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SADEGH-NASSERI, SCHEHERAZADE · 1998 to 2007
$1.9M
NIAID NIH HHS R01 AI063764NIAID NIH HHS R01AI063764NIGMS NIH HHS R01 GM053549NIGMS NIH HHS R01GM53549
6 · The paper itself

Abstract

The peptide editor HLA-DM (DM) catalyzes the exchange of peptides bound to MHC class II molecules within antigen presenting cells by generating a "peptide-receptive" MHC class II conformation (MHC(receptive)) to which peptides readily bind and rapidly unbind. While recent work has uncovered the determinants of DM recognition and effector functions, the nature of MHC(receptive) and its interaction with DM remains unclear. Here, we show that DM induces but does not stabilize MHC(receptive) in the absence of peptides. We demonstrate that DM is out-competed by certain superantigens, and increasing solvent viscosity inhibits DM-induced peptide association. We suggest that DM mediates peptide exchange by interacting transiently and repeatedly with MHC class II molecules, continually generating MHC(receptive). The simultaneous presence of peptide and DM in the milieu is thus crucial for the efficient generation of specific peptide-MHC class II complexes over time.

Indexed as

HLA-D AntigensHLA-DR1 AntigenHumansPeptidesSuperantigensHLA-D AntigensHLA-DM antigensHLA-DR1 AntigenPeptidesSuperantigens

Identifiers

PMID19647320
PMCPMC2743474
OpenAlexW2165460177

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.