Evidence map›Paper›PMID 19834548›Full record

ArticlePLoS pathogens2009

Coxsackievirus B3 inhibits antigen presentation in vivo, exerting a profound and selective effect on the MHC class I pathway.

Christopher C Kemball, Stephanie Harkins, Jason K Whitmire, Claudia T Flynn, Ralph Feuer, J Lindsay Whitton

Abstract read
In one paragraph

Article in PLoS pathogens, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. SARS-CoV-2 accessory proteins ORF7a and ORF3a use distinct mechanisms to down-regulate MHC-I surface expression.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. A viral-specific CD4Frontiers in immunology · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Murine Models of Hepatitis A Virus Infection.Cold Spring Harbor perspectives in medicine · 2019
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

6 authors.

Christopher C KemballDepartment of Immunology and Microbial Science, SP30-2110, The Scripps Research Institute, La Jolla, CA, USA.
Stephanie Harkins
Jason K Whitmire
Claudia T Flynn
Ralph Feuer
J Lindsay Whitton

Funding

COXSACKIE MYOCARDITIS AND VIRAL PERSISTENCE IN THE HEARTR01AI042314 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI WHITTON, J. LINDSAY · 1998 to 2013
$5.6M
Virology of the Central Nervous SystemT32NS041219 · NINDS · SCRIPPS RESEARCH INSTITUTE, THE · PI ELDER, JOHN H · 2001 to 2010
$2.4M
Analyses of the effects of pro-inflammatory cytokines on CD4+ T cell responsesR01AI074862 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI WHITMIRE, JASON KYLE · 2008 to 2012
$1.6M
NIAID NIH HHS R01 AI-042314NIAID NIH HHS R01 AI042314NIAID NIH HHS R01 AI-074862NIAID NIH HHS R01 AI074862NINDS NIH HHS T32 NS041219NINDS NIH HHS T32 NS41219
6 · The paper itself

Abstract

Many viruses encode proteins whose major function is to evade or disable the host T cell response. Nevertheless, most viruses are readily detected by host T cells, and induce relatively strong T cell responses. Herein, we employ transgenic CD4(+) and CD8(+) T cells as sensors to evaluate in vitro and in vivo antigen presentation by coxsackievirus B3 (CVB3), and we show that this virus almost completely inhibits antigen presentation via the MHC class I pathway, thereby evading CD8(+) T cell immunity. In contrast, the presentation of CVB3-encoded MHC class II epitopes is relatively unencumbered, and CVB3 induces in vivo CD4(+) T cell responses that are, by several criteria, phenotypically normal. The cells display an effector phenotype and mature into multi-functional CVB3-specific memory CD4(+) T cells that expand dramatically following challenge infection and rapidly differentiate into secondary effector cells capable of secreting multiple cytokines. Our findings have implications for the efficiency of antigen cross-presentation during coxsackievirus infection.

Indexed as

AnimalsAntigen PresentationCD4-Positive T-LymphocytesCells, CulturedCoxsackievirus InfectionsEnterovirus B, HumanEpitopesHeLa CellsHistocompatibility Antigens Class IHumansImmunologic MemoryMaleMiceMice, Inbred C57BLMice, TransgenicReceptors, Antigen, T-CellEpitopesHistocompatibility Antigens Class IReceptors, Antigen, T-Cell

Identifiers

PMID19834548
PMCPMC2757675

What OpenQuestion holds

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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.