Evidence map›Paper›PMID 12368467›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Existing antivirals are effective against influenza viruses with genes from the 1918 pandemic virus.

Terrence M Tumpey, Adolfo García-Sastre, Andrea Mikulasova, Jeffery K Taubenberger, David E Swayne, Peter Palese, Christopher F Basler

Abstract readHistorical Article
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. COVID-19: Antiviral agents and enzyme inhibitors/receptor blockers in development.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  5. Review
  6. The 1918 Influenza Pandemic and Its Legacy.Cold Spring Harbor perspectives in medicine · 2020
    Review
  7. The Rationale for Potential Pharmacotherapy of COVID-19.Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Structure and mechanism of proton transport through the transmembrane tetrameric M2 protein bundle of the influenza A virus.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  20. Analysis of in vivo dynamics of influenza virus infection in mice using a GFP reporter virus.Proceedings of the National Academy of Sciences of the United States of America · 2010
    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

7 authors.

Terrence M TumpeySoutheast Poultry Research Laboratory, United States Department of Agriculture, Athens, GA 30605, USA.
Adolfo García-Sastre
Andrea Mikulasova
Jeffery K Taubenberger
David E Swayne
Peter Palese
Christopher F Basler

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The 1918 influenza pandemic caused more than 20 million deaths worldwide. Thus, the potential impact of a re-emergent 1918 or 1918-like influenza virus, whether through natural means or as a result of bioterrorism, is of significant concern. The genetic determinants of the virulence of the 1918 virus have not been defined yet, nor have specific clinical prophylaxis and/or treatment interventions that would be effective against a re-emergent 1918 or 1918-like virus been identified. Based on the reported nucleotide sequences, we have reconstructed the hemagglutinin (HA), neuraminidase (NA), and matrix (M) genes of the 1918 virus. Under biosafety level 3 (agricultural) conditions, we have generated recombinant influenza viruses bearing the 1918 HA, NA, or M segments. Strikingly, recombinant viruses possessing both the 1918 HA and 1918 NA were virulent in mice. In contrast, a control virus with the HA and NA from a more recent human isolate was unable to kill mice at any dose tested. The recombinant viruses were also tested for their sensitivity to U.S. Food and Drug Administration-approved antiinfluenza virus drugs in vitro and in vivo. Recombinant viruses possessing the 1918 NA or both the 1918 HA and 1918 NA were inhibited effectively in both tissue culture and mice by the NA inhibitors, zanamivir and oseltamivir. A recombinant virus possessing the 1918 M segment was inhibited effectively both in tissue culture and in vivo by the M2 ion-channel inhibitors amantadine and rimantadine. These data suggest that current antiviral strategies would be effective in curbing the dangers of a re-emergent 1918 or 1918-like virus.

Indexed as

Genes, ViralAmantadineAnimalsAntiviral AgentsDisease OutbreaksEnzyme InhibitorsHemagglutinin Glycoproteins, Influenza VirusHistory, 20th CenturyHumansInfluenza A virusInfluenza, HumanMaleMiceMice, Inbred BALB CNeuraminidaseRecombination, GeneticAmantadineAntiviral AgentsEnzyme InhibitorsHemagglutinin Glycoproteins, Influenza VirusM2 protein, Influenza A virusM-protein, influenza virusNeuraminidaseRimantadineViral Matrix ProteinsViroporin Proteins

Identifiers

PMID12368467
PMCPMC129786

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.