Evidence map›Paper›PMID 31034515›Full record

ArticlePLoS pathogens2019

Molluscum contagiosum virus MC80 sabotages MHC-I antigen presentation by targeting tapasin for ER-associated degradation.

Ian B Harvey, Xiaoli Wang, Daved H Fremont

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. 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
2.1field-weighted citation impact, top 13% 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, 27 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
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  7. Genetic variation that determinesProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Immunogenic cell stress and death.Nature immunology · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. HLA polymorphism and tapasin independence influence outcomes of HIV and dengue virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. HLA tapasin independence: broader peptide repertoire and HIV control.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  14. Article
  15. Article
  16. Review
  17. Article
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

3 authors at 1 institution in 1 country.

Ian B HarveyDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.ORCID 0000-0002-5444-8287
Xiaoli WangDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Daved H FremontDepartment of Pathology & Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.ORCID 0000-0002-8544-2689
Washington University in St. Louis · US

Funding

Infectious Diseases/Basic Microbial Pathogenic MechanismsT32AI007172 · NIAID · WASHINGTON UNIVERSITY · PI Daniel E. Goldberg, JENNIFER A PHILIPS · 1985 to 2026
$13.0M
T Cell Control by Cowpoxvirus U19AI109948 · NIAID · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 2014 to 2018
$6.4M
MHC-I regulation by herpes virusR01AI019687 · NIAID · WASHINGTON UNIVERSITY · PI FREMONT, DAVED H. · 1985 to 2016
$5.2M
NIAID NIH HHS R01 AI019687NIAID NIH HHS T32 AI007172NIAID NIH HHS U19 AI109948
6 · The paper itself

Abstract

The human specific poxvirus molluscum contagiosum virus (MCV) produces skin lesions that can persist with minimal inflammation, suggesting that the virus has developed robust immune evasion strategies. However, investigations into the underlying mechanisms of MCV pathogenesis have been hindered by the lack of a model system to propagate the virus. Herein we demonstrate that MCV-encoded MC80 can disrupt MHC-I antigen presentation in human and mouse cells. MC80 shares moderate sequence-similarity with MHC-I and we find that it associates with components of the peptide-loading complex. Expression of MC80 results in ER-retention of host MHC-I and thereby reduced cell surface presentation. MC80 accomplishes this by engaging tapasin via its luminal domain, targeting it for ubiquitination and ER-associated degradation in a process dependent on the MC80 transmembrane region and cytoplasmic tail. Tapasin degradation is accompanied by a loss of TAP, which limits MHC-I access to cytosolic peptides. Our findings reveal a unique mechanism by which MCV undermines adaptive immune surveillance.

Indexed as

Endoplasmic Reticulum-Associated DegradationAnimalsAntigen PresentationATP Binding Cassette Transporter, Subfamily B, Member 2Cells, CulturedEndoplasmic ReticulumHistocompatibility Antigens Class IHumansImmune EvasionMembrane Transport ProteinsMiceMolluscum ContagiosumMolluscum contagiosum virusT-Lymphocytes, CytotoxicViral ProteinsATP Binding Cassette Transporter, Subfamily B, Member 2Histocompatibility Antigens Class IMembrane Transport ProteinstapasinViral Proteins

Identifiers

PMID31034515
PMCPMC6508746
OpenAlexW2943634992

What Socratic 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 Socratic graph.