Evidence map›Paper›PMID 21333491›Full record

ArticleJournal of autoimmunity2011

Nasal cardiac myosin peptide treatment and OX40 blockade protect mice from acute and chronic virally-induced myocarditis.

Georgia Fousteri, Amy Dave, Bret Morin, Shaida Omid, Michael Croft, Matthias G von Herrath

Abstract read
In one paragraph

Article in Journal of autoimmunity, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Myocarditis in Humans and in Experimental Animal Models.Frontiers in cardiovascular medicine · 2019
    Review
  7. Review
  8. Berberine Restricts Coxsackievirus B Type 3 Replication via Inhibition of c-Jun N-Terminal Kinase (JNK) and p38 MAPK Activation In Vitro.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  9. Review
  10. Review
  11. Article
  12. OX40L blockade is therapeutic in arthritis, despite promoting osteoclastogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. Review
  14. Review
  15. Review
  16. The autoimmune side of heart and lung diseases.Clinical reviews in allergy & immunology · 2013
    Review
  17. Article
  18. Autoimmunity in 2011.Clinical reviews in allergy & immunology · 2012
    Review
  19. Update on coxsackievirus B3 myocarditis.Current opinion in rheumatology · 2012
    Review
  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 at 1 institution in 1 country.

Georgia FousteriDiabetes Center, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Amy Dave
Bret Morin
Shaida Omid
Michael Croft
Matthias G von Herrath
La Jolla Institute for Immunology · US

Funding

Treg stability in viral infection and autoimmunityP01AI089624 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI PETERS, BJOERN · 2010 to 2014
$10.1M
Viruses and Autoimmunity POIP01AI058105 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI VON HERRATH, MATTHIAS G. · 2004 to 2009
$6.0M
Regulation of T Cell Tolerance by OX40R01CA091837 · NCI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2002 to 2012
$2.5M
TNFR Members in T Cell Immunity to VacciniaR01AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2006 to 2010
$2.3M
How IL-10R blockade can resolve persistent viral infectionsR01AI068818 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI VON HERRATH, MATTHIAS G. · 2007 to 2010
$1.9M
TNFR Members in T Cell Immunity to VacciniaR56AI067341 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI CROFT, MICHAEL · 2012 to 2012
$348k
NCI NIH HHS CA91837NCI NIH HHS R01 CA091837NIAID NIH HHS AI67341NIAID NIH HHS P01 AI058105NIAID NIH HHS P01 AI089624NIAID NIH HHS R01 AI067341NIAID NIH HHS R01 AI068818NIAID NIH HHS R56 AI067341
6 · The paper itself

Abstract

Myocarditis poses a severe health problem, can lead to dilated cardiomyopathy (DCM) and death, and is thought to be triggered by infections. Enteroviruses such as Coxsackie virus B3 (CVB3) have been implicated as a culprit, since they can cause acute and chronic heart disease in susceptible mice. CVB was detected in human cardiac myocytes in some cases, whereas acute CVB infection was thought to have caused death. Here we studied, whether nasal administration of cardiac myosin (CM) major histocompatibility class (MHC) II peptides CM₉₄₇-₉₆₀ and CM₇₃₅-₇₄₇ and OX40 blockade would be able to ameliorate immunopathology and heart disease in BALB/C mice infected with CVB3. We found that nasal CM-peptide prophylactic treatment significantly reduced myocarditis and mortality by enhancing Treg and IL-10 induction and that blockade of OX40 signaling could reduce heart inflammation when administered late during pathogenesis. Altogether, these results chart the way for novel prevention and intervention strategies for viral myocarditis.

Indexed as

Enterovirus B, HumanAcute DiseaseAdministration, IntranasalAnimalsAutoimmune DiseasesCardiac MyosinsChronic DiseaseCoxsackievirus InfectionsInterleukin-10MaleMiceMice, Inbred BALB CMyocarditisReceptors, OX40SpleenT-Lymphocytes, RegulatoryCardiac MyosinsInterleukin-10Receptors, OX40Tnfrsf4 protein, mouse

Identifiers

PMID21333491
PMCPMC3079777
OpenAlexW2099959908

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.