Evidence map›Paper›PMID 27891529›Full record

ArticleInternational journal of virology studies & research2015

Novel Approaches to the Prevention and Treatment of Rabies.

C W Gnanadurai, C T Huang, D Kumar, Zhen F Fu

Open access · diamondAbstract read
In one paragraph

Article in International journal of virology studies & research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Optimization of Inhibitory Peptides Targeting Phosphoprotein of Rabies Virus.International journal of peptide research and therapeutics · 2020
    Article
  4. Article
  5. 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

4 authors at 1 institution in 2 countries.

C W GnanaduraiDepartment of Pathology, College of Veterinary Medicine, University of Georgia Athens, USA.
C T HuangDepartment of Pathology, College of Veterinary Medicine, University of Georgia Athens, USA.
D KumarDepartment of Pathology, College of Veterinary Medicine, University of Georgia Athens, USA.
Zhen F FuDepartment of Pathology, College of Veterinary Medicine, University of Georgia Athens, USA; State-key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, China.
University of Georgia · US

Funding

Virus Clearance from the Central Nervous SystemR01AI093369 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI FU, ZHEN F, HOOPER, DOUGLAS CRAIG · 2011 to 2015
$4.7M
Developing Avirulent Rabies Virus VaccinesR01AI051560 · NIAID · UNIVERSITY OF GEORGIA (UGA) · PI FU, ZHEN F · 2002 to 2010
$2.0M
NIAID NIH HHS R01 AI051560NIAID NIH HHS R01 AI093369
6 · The paper itself

Abstract

Rabies is a highly lethal disease caused by the neurotropic rabies virus (RABV), and it remains an important public health problem globally. Effective vaccines have been developed for pre- and post-exposure prophylaxis (PEP). PEP is only effective if it is initiated promptly after recognizing exposure. Once neurological symptoms develop, however, it is widely accepted that there is no effective treatment available. Recent studies indicate that the presence of RABV-specific immunity (i.e. Virus neutralizing antibodies, VNA) and the transient enhancement of the BBB permeability are absolutely required for effective virus clearance from the CNS. In principle, it has been shown in mice using various live-attenuated RABVs or recombinant RABVs expressing three copies of the G or expressing chemokine/cytokines, which can induce high levels of VNA in the serum and also capable of transiently enhancing the BBB permeability that it is possible to clear the virus from CNS. Also, it has been demonstrated that, intravenous administration of VNA together with MCP-1 (shown to transiently open up BBB) can clear RABV from the CNS in both immunocompetent and immunocompromised mice, as late as 5 days after lethal challenge. Novel therapeutic approaches aimed at allowing the peripheral VNA to cross the BBB by administration of the VNA in combination with biological or chemical agents that can transiently open up the BBB would be useful to establish an effective therapy for rabies in humans. In this review, we focus on the some of the approaches that can be used to meet the challenges in the field of rabies treatment.

Indexed as

Blood-Brain BarrierPathogenesisPost-Exposure ProphylaxisRabies VirusTherapyTreatmentVirus Neutralizing Antibodies

Identifiers

PMID27891529
PMCPMC5123589
OpenAlexW2186329727

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.