Evidence map›Paper›PMID 23813435›Full record

ReviewBioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy2013

Emerging targets and novel approaches to Ebola virus prophylaxis and treatment.

Jin Huk Choi, Maria A Croyle

Abstract readReview
In one paragraph

Review in BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing 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

40 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Nucleic Acid-Based Technologies Targeting Coronaviruses.Trends in biochemical sciences · 2021
    Review
  9. Review
  10. Viral Pandemics of the Last Four Decades: Pathophysiology, Health Impacts and Perspectives.International journal of environmental research and public health · 2020
    Review
  11. A review on current status of antiviral siRNA.Reviews in medical virology · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Particulate delivery systems for vaccination against bioterrorism agents and emerging infectious pathogens.Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology · 2017
    Review
  18. Review
  19. Review
  20. 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

2 authors.

Jin Huk ChoiDivision of Pharmaceutics, The University of Texas at Austin, College of Pharmacy, PHR 4.214D, 2409 W. University Ave., 1 University Station #A1920, Austin, TX, 78712-1074, USA.
Maria A Croyle

Funding

Evaluation of Protective Immunity After Mucosal Vaccination Against Ebola VirusU01AI078045 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI CROYLE, MARIA A · 2008 to 2012
$2.5M
NIAID NIH HHS U01 AI078045NIAID NIH HHS U01AI078045
6 · The paper itself

Abstract

Ebola is a highly virulent pathogen causing severe hemorrhagic fever with a high case fatality rate in humans and non-human primates (NHPs). Although safe and effective vaccines or other medicinal agents to block Ebola infection are currently unavailable, a significant effort has been put forth to identify several promising candidates for the treatment and prevention of Ebola hemorrhagic fever. Among these, recombinant adenovirus-based vectors have been identified as potent vaccine candidates, with some affording both pre- and post-exposure protection from the virus. Recently, Investigational New Drug (IND) applications have been approved by the US Food and Drug Administration (FDA) and phase I clinical trials have been initiated for two small-molecule therapeutics: anti-sense phosphorodiamidate morpholino oligomers (PMOs: AVI-6002, AVI-6003) and lipid nanoparticle/small interfering RNA (LNP/siRNA: TKM-Ebola). These potential alternatives to vector-based vaccines require multiple doses to achieve therapeutic efficacy, which is not ideal with regard to patient compliance and outbreak scenarios. These concerns have fueled a quest for even better vaccination and treatment strategies. Here, we summarize recent advances in vaccines or post-exposure therapeutics for prevention of Ebola hemorrhagic fever. The utility of novel pharmaceutical approaches to refine and overcome barriers associated with the most promising therapeutic platforms are also discussed.

Indexed as

AdenoviridaeAnimalsDrug DesignEbola VaccinesEbolavirusGenetic VectorsHemorrhagic Fever, EbolaHumansMedication AdherenceMolecular Targeted TherapyOligonucleotides, AntisensePost-Exposure ProphylaxisRNA, Small InterferingEbola VaccinesOligonucleotides, AntisenseRNA, Small Interfering

Identifiers

PMID23813435
PMCPMC3833964

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.