Evidence map›Paper›PMID 23243279›Full record

ArticleBlood2013

A catalytically inactive mutant of the deubiquitylase YOD-1 enhances antigen cross-presentation.

Sharvan Sehrawat, Paul-Albert Koenig, Oktay Kirak, Christian Schlieker, Manuel Fankhauser, Hidde L Ploegh

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  15. Deubiquitinase YOD1 potentiates YAP/TAZ activities through enhancing ITCH stability.Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

6 authors at 3 institutions in 1 country.

Sharvan SehrawatWhitehead Institute for Biomedical Research, Cambridge, MA 02142, USA.
Paul-Albert Koenig
Oktay Kirak
Christian Schlieker
Manuel Fankhauser
Hidde L Ploegh
Whitehead Institute for Biomedical Research · USScripps Research Institute · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antigen presenting cells (APCs) that express a catalytically inactive version of the deubiquitylase YOD1 (YOD1-C160S) present exogenous antigens more efficiently to CD8(+) T cells, both in vitro and in vivo. Compared with controls, immunization of YOD1-C160S mice led to greater expansion of specific CD8(+) T cells and showed improved control of infection with a recombinant -herpes virus, MHV-68, engineered to express SIINFEKL peptide, the ligand for the ovalbumin-specific TCR transgenic OT-I cells. Enhanced expansion of specific CD8(+) T cells was likewise observed on infection of YOD1-C160S mice with a recombinant influenza A virus expressing SIINFEKL. YOD1-C160S APCs retained antigen longer than did control APCs. Enhanced crosspresentation by YOD1-C160S APCs was transporter associated with antigen processing (TAP1)-independent but sensitive to inclusion of inhibitors of acidification and of the proteasome. The activity of deubiquitylating enzymes may thus help control antigenspecific CD8(+) T-cell responses during immunization.

Indexed as

Cross-PrimingMutation, MissenseAdoptive TransferAnimalsAntigen-Presenting CellsATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2Brefeldin ACD8-Positive T-LymphocytesFemaleHydrogen-Ion ConcentrationImmunizationMaleMiceMice, Inbred C57BLMice, KnockoutATP-Binding Cassette TransportersATP Binding Cassette Transporter, Subfamily B, Member 2Brefeldin AOVA-8OvalbuminPeptide FragmentsTap1 protein, mouseUbiquitin Thiolesterase

Identifiers

PMID23243279
PMCPMC3575758
OpenAlexW2016505377

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.