Evidence map›Paper›PMID 30541829›Full record

ArticleJournal of virology2019

Novel Modified Vaccinia Virus Ankara Vector Expressing Anti-apoptotic Gene

Lynette S Chea, Linda S Wyatt, Sailaja Gangadhara, Bernard Moss, Rama R Amara

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 11 citations in OpenAlex.

  1. Monkeypox virus protein OPG188 antagonizes cGAS-STING antiviral signaling pathway to mediate immune evasion.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

5 authors at 2 institutions in 1 country.

Lynette S CheaDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Linda S WyattLaboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Sailaja GangadharaDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA.
Bernard MossLaboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0002-2154-8564
Rama R AmaraDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia, USA ramara@emory.edu.
Emory University · USNational Institutes of Health · US

Funding

Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI RENGARAJAN, JYOTHI · 1985 to 2011
$114.0M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Ann M Chahroudi, Colleen F Kelley · 2002 to 2026
$74.0M
Recombinant Virus VaccinesZIAAI000416 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI MOSS, BERNARD · 2009 to 2025
$17.3M
Preclinical Studies and T cell ResponsesU19AI109633 · NIAID · EMORY UNIVERSITY · PI VELU, VIJAYAKUMAR · 2014 to 2018
$10.2M
Optimizing Adjuvants and Needle Free Delivery Methods for Oral HIV VaccinationR01DE026333 · NIDCR · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2016 to 2020
$4.7M
DENTAL, ORAL AND CRANIOFACIAL DATA RESOURCE CENTERN01DE002633 · NIDCR · NORTHRUP GRUMMAN INFORM TECH CORP · PI REICHMAN, MARSHA · 2000 to 2000
$871k
NCRR NIH HHS P51 RR000165NHLBI NIH HHS N01 DE002633NIAID NIH HHS P30 AI050409NIAID NIH HHS U19 AI109633NIDCR NIH HHS R01 DE026333NIH HHS P51 OD011132
6 · The paper itself

Abstract

Modified vaccinia virus Ankara (MVA), an attenuated poxvirus, has been developed as a potential vaccine vector for use against cancer and multiple infectious diseases, including human immunodeficiency virus (HIV). MVA is highly immunogenic and elicits strong cellular and humoral responses in preclinical models and humans. However, there is potential to further enhance the immunogenicity of MVA, as MVA-infected cells undergo rapid apoptosis, leading to faster clearance of recombinant antigens and potentially blunting a greater response. Here, we generated MVA-

Indexed as

AnimalsApoptosisCell Line, TumorDendritic Cellsenv Gene Products, Human Immunodeficiency VirusFemaleGene Products, gagGene Products, polHeLa CellsHumansMacaca mulattaMiceMice, Inbred BALB CVaccinia virusViral ProteinsViral Vaccinesenv Gene Products, Human Immunodeficiency VirusGene Products, gagGene Products, polViral ProteinsViral Vaccinesantibody responsesmodified vaccinia virus AnkaraMVApoxvirusvaccineviral vector

Identifiers

PMID30541829
PMCPMC6384055
OpenAlexW2905519969

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.