Evidence map›Paper›PMID 20004216›Full record

ArticleAntiviral research2010

Antiviral prevention of sepsis induced cytomegalovirus reactivation in immunocompetent mice.

Meghan R Forster, Joanne Trgovcich, Peter Zimmerman, Alexander Chang, Cortland Miller, Paul Klenerman, Charles H Cook

Abstract read
In one paragraph

Article in Antiviral research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 29 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Impaired polyfunctionality of CD8Experimental & molecular medicine · 2017
    Article
  7. Article
  8. Article
  9. Sepsis and cytomegalovirus: foes or conspirators?Medical microbiology and immunology · 2015
    Review
  10. Resistant pathogens, fungi, and viruses.The Surgical clinics of North America · 2014
    Review
  11. Article
  12. Review
  13. [Ventilator-associated viral pneumonia].Reanimation : journal de la Societe de reanimation de langue francaise · 2011
    Article
  14. 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

7 authors at 2 institutions in 2 countries.

Meghan R ForsterDepartment of Surgery, The Ohio State University, Columbus, OH 43210, United States.
Joanne Trgovcich
Peter Zimmerman
Alexander Chang
Cortland Miller
Paul Klenerman
Charles H Cook
The Ohio State University · USUniversity of Oxford · GB

Funding

Bacterial Sepsis & Reactivation of Latent CytomegalovirusR01GM066115 · NIGMS · OHIO STATE UNIVERSITY · PI COOK, CHARLES H · 2003 to 2014
$2.6M
NIGMS NIH HHS R01 GM066115NIGMS NIH HHS R01GM066115
6 · The paper itself

Abstract

introductionImmunocompetent patients can reactivate latent cytomegalovirus (CMV) during critical illness and reactivation is associated with significantly worse outcomes. Prior to clinical trials in humans to prove causality, we sought to determine an optimal antiviral treatment strategy.

methodsMice latently infected with murine CMV (MCMV) received a septic reactivation trigger and were randomized to receive one of four ganciclovir regimens or saline. Lungs were evaluated for viral transcriptional reactivation and fibrosis after each regimen. Influences of ganciclovir on early sepsis-induced pulmonary inflammation and T-cell activation were studied after sepsis induction.

resultsAll ganciclovir regimens reduced measurable MCMV transcriptional reactivation, and 10mg/day for 7 or 21 days was most effective. Lower dose (5mg/kg/day) or delayed therapy was associated with significant breakthrough reactivation. Higher doses of ganciclovir given early were associated with the lowest incidence of pulmonary fibrosis, and delay of therapy for 1 week was associated with significantly worse pulmonary fibrosis. Although bacterial sepsis induced activation of MCMV-specific pulmonary T-cells, this activation was not influenced by ganciclovir.

conclusionThese results suggest that antiviral treatment trials in humans should use 10mg/kg/day ganciclovir administered as early as possible in at-risk patients to minimize reactivation events and associated pulmonary injury.

Indexed as

Virus ActivationAnimalsAntiviral AgentsCytomegalovirus InfectionsDisease Models, AnimalFemaleGanciclovirHumansLungMiceMice, Inbred BALB CMuromegalovirusRandom AllocationSepsisAntiviral AgentsGanciclovir

Identifiers

PMID20004216
PMCPMC2830346
OpenAlexW2042436918

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.