Evidence map›Paper›PMID 25298110›Full record

ArticleClinical and vaccine immunology : CVI2014

Immunologic characterization of a rhesus macaque H1N1 challenge model for candidate influenza virus vaccine assessment.

Jason A Skinner, Sandra M Zurawski, Chie Sugimoto, Heather Vinet-Oliphant, Parvathi Vinod, Yaming Xue, Kasi Russell-Lodrigue, Randy A Albrecht, Adolfo García-Sastre, Andres M Salazar and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2014. 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
2.4field-weighted citation impact, top 12% 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, 28 citations in OpenAlex.

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  12. The Legacy of CVI.Clinical and vaccine immunology : CVI · 2017
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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

14 authors at 3 institutions in 1 country.

Jason A SkinnerBaylor Institute for Immunology Research, Dallas, Texas, USA.
Sandra M ZurawskiBaylor Institute for Immunology Research, Dallas, Texas, USA.
Chie SugimotoTulane National Primate Research Center, Covington, Louisiana, USA.
Heather Vinet-OliphantTulane National Primate Research Center, Covington, Louisiana, USA.
Parvathi VinodBaylor Institute for Immunology Research, Dallas, Texas, USA.
Yaming XueBaylor Institute for Immunology Research, Dallas, Texas, USA.
Kasi Russell-LodrigueTulane National Primate Research Center, Covington, Louisiana, USA.
Randy A AlbrechtIcahn School of Medicine at Mount Sinai, New York, New York, USA.
Adolfo García-SastreIcahn School of Medicine at Mount Sinai, New York, New York, USA.
Andres M SalazarOncovir, Inc., Washington, DC, USA.
Chad J RoyTulane National Primate Research Center, Covington, Louisiana, USA.
Marcelo J KurodaTulane National Primate Research Center, Covington, Louisiana, USA.
SangKon OhBaylor Institute for Immunology Research, Dallas, Texas, USA.
Gerard ZurawskiBaylor Institute for Immunology Research, Dallas, Texas, USA gerardz@baylorhealth.edu.
Tulane University · USIcahn School of Medicine at Mount Sinai · USOncovir (United States) · US

Funding

Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI LEGRAND, ROGER · 2003 to 2013
$49.2M
Vaccine Induced Activation of T Follicular Helper Cell SubsetsU19AI089987 · NIAID · BAYLOR RESEARCH INSTITUTE · PI PASCUAL, MARIA VIRGINIA · 2010 to 2015
$17.0M
NIAID NIH HHS 5U19AI057234NIAID NIH HHS 5U19AI057234S2NIAID NIH HHS 5U19AI057234S3NIAID NIH HHS 5U19AI089987NIAID NIH HHS U19 AI057234NIAID NIH HHS U19 AI089987NIH HHS OD-011104-51NIH HHS P51 OD011104
6 · The paper itself

Abstract

Despite the availability of annually formulated vaccines, influenza virus infection remains a worldwide public health burden. Therefore, it is important to develop preclinical challenge models that enable the evaluation of vaccine candidates while elucidating mechanisms of protection. Here, we report that naive rhesus macaques challenged with 2009 pandemic H1N1 (pH1N1) influenza virus do not develop observable clinical symptoms of disease but develop a subclinical biphasic fever on days 1 and 5 to 6 postchallenge. Whole blood microarray analysis further revealed that interferon activity was associated with fever. We then tested whether type I interferon activity in the blood is a correlate of vaccine efficacy. The animals immunized with candidate vaccines carrying hemagglutinin (HA) or nucleoprotein (NP) exhibited significantly reduced interferon activity on days 5 to 6 postchallenge. Supported by cellular and serological data, we conclude that blood interferon activity is a prominent marker that provides a convenient metric of influenza virus vaccine efficacy in the subclinical rhesus macaque model.

Indexed as

AnimalsAntibodies, ViralHumansImmunizationInfluenza A Virus, H1N1 SubtypeInfluenza, HumanInfluenza VaccinesMacaca mulattaOrthomyxoviridae InfectionsVaccinationAntibodies, ViralInfluenza Vaccines

Identifiers

PMID25298110
PMCPMC4248778
OpenAlexW2107834199

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.