Evidence map›Paper›PMID 16924471›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2006

Treatment of coxsackievirus-B3-infected BALB/c mice with the soluble coxsackie adenovirus receptor CAR4/7 aggravates cardiac injury.

A Dörner, H-P Grunert, V Lindig, K Chandrasekharan, H Fechner, K U Knowlton, A Isik, M Pauschinger, H Zeichhardt, H-P Schultheiss

Abstract read
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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. CAR-diology--a virus receptor in the healthy and diseased heart.Journal of molecular medicine (Berlin, Germany) · 2009
    Article
  11. 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

10 authors at 2 institutions in 2 countries.

A DörnerDepartment of Cardiology and Pneumonology, Charité University of Medicine, Campus Benjamin Franklin, Hindenburgdamm 30, 12200, Berlin, Germany. andrea.doerner@charite.de
H-P Grunert
V Lindig
K Chandrasekharan
H Fechner
K U Knowlton
A Isik
M Pauschinger
H Zeichhardt
H-P Schultheiss
Charité - Universitätsmedizin Berlin · DEUniversity of California, San Diego · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coxsackie adenovirus receptor (CAR) is involved in immunological processes, and its soluble isoforms have antiviral effects on coxsackievirus B3 (CVB3) infection in vitro. We explored in this study the impact of CAR4/7, a soluble CAR isoform, on CVB3-induced myocarditis in BALB/c mice. BALB/c mice were treated daily with recombinant CAR4/7, beta-galactosidase (beta-Gal; as control protein) or buffer for 9 days. Half of each group was infected with CVB3 on day 3, and all mice were killed on day 9. Myocardial CVB3 titer, histology, and serology were analyzed. Treatment with CAR4/7 led to a significant reduction of myocardial CVB3 titer, whereas the application of beta-Gal had no detectable effect on the myocardial virus load. CAR4/7 application, however, resulted in increased myocardial inflammation and tissue damage in CVB3-infected hearts, whereas beta-Gal caused a degree of cardiac inflammation and injury similar to that in buffer-treated CVB3-infected control animals. CAR4/7 and beta-Gal treatment induced the production of antibodies against the respective antigens. CAR4/7-, but not beta-Gal-specific, virus-negative sera reacted against myocardial tissue and cellular membranous CAR, and significantly inhibited CVB3 infection in vitro. Thus, CAR4/7 suppressed CVB3 infection in vivo, supporting the concept of receptor analog in antiviral therapy. However, CAR4/7 treatment also leads to an aggravation of myocardial inflammation and injury most likely secondary to an autoimmune process.

Indexed as

AnimalsAntiviral AgentsCell SurvivalCoxsackie and Adenovirus Receptor-Like Membrane ProteinCoxsackievirus InfectionsCreatine KinaseEnterovirus B, HumanEnzyme-Linked Immunosorbent AssayHeLa CellsHumansImmune SeraImmunohistochemistryInjections, IntraperitonealMaleMiceMice, Inbred BALB CAntiviral AgentsCLMP protein, humanCLMP protein, mouseCoxsackie and Adenovirus Receptor-Like Membrane ProteinCreatine KinaseImmune SeraReceptors, VirusRecombinant ProteinsSerum Amyloid A Protein

Identifiers

PMID16924471
OpenAlexW2137241376

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.