Evidence map›Paper›PMID 23269785›Full record

ArticleJournal of virology2013

A vesicular stomatitis virus-based therapeutic vaccine generates a functional CD8 T cell response to hepatitis B virus in transgenic mice.

Melissa A Cobleigh, Xin Wei, Michael D Robek

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. CD4Nature immunology · 2025
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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

3 authors at 2 institutions in 2 countries.

Melissa A CobleighDepartment of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
Xin Wei
Michael D Robek
Yale University · USAir Force Medical University · CN

Funding

Viral Vaccine Vectors to Prevent Hepatocellular CarcinomaR01CA131133 · NCI · YALE UNIVERSITY · PI ROBEK, MICHAEL · 2008 to 2011
$1.1M
NCI NIH HHS CA131133NCI NIH HHS R01 CA131133
6 · The paper itself

Abstract

Recombinant vesicular stomatitis virus (VSV) is a promising therapeutic vaccine platform. Using a transgenic mouse model of chronic hepatitis B virus (HBV) infection, we evaluated the therapeutic potential of a VSV vector expressing the HBV middle surface envelope glycoprotein (MS). VSV-MS immunization generated HBV-specific CD8 T cell and antibody responses in transgenic mice that express low HBV antigen levels. These findings support the further development of VSV as a therapeutic vaccine vector for chronic HBV.

Indexed as

AnimalsCD8-Positive T-LymphocytesHepatitis BHepatitis B Surface AntigensHepatitis B VaccinesHepatitis B virusMiceMice, TransgenicVesicular stomatitis Indiana virusViral Envelope ProteinsHepatitis B Surface AntigensHepatitis B Vaccinesmiddle envelope protein, Hepatitis B virusViral Envelope Proteins

Identifiers

PMID23269785
PMCPMC3571382
OpenAlexW2013799252

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.