Evidence map›Paper›PMID 26044496›Full record

ArticleVaccine2015

Competitive detection of influenza neutralizing antibodies using a novel bivalent fluorescence-based microneutralization assay (BiFMA).

Steven F Baker, Aitor Nogales, Felix W Santiago, David J Topham, Luis Martínez-Sobrido

Abstract read
In one paragraph

Article in Vaccine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

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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.

Steven F BakerDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, United States.
Aitor NogalesDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, United States.
Felix W SantiagoDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, United States.
David J TophamDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, United States.
Luis Martínez-SobridoDepartment of Microbiology and Immunology, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, United States. Electronic address: luis_martinez@urmc.rochester.edu.

Funding

The T32 Predoctoral Training Program in Immunology (PTPI)T32AI007285 · NIAID · UNIVERSITY OF ROCHESTER · PI Scott Andrew Gerber, JACQUES Robert · 1986 to 2026
$7.6M
Aza Sisters: An HIV Prevention Program for African American GirlsR21NR010511 · NINR · GEORGETOWN UNIVERSITY · PI TOWNSEND, TIFFANY G. · 2007 to 2008
$418k
Single-cycle Infectious Candid#1 to Study Hemorrhagic Fever New World ArenavirusR03AI099681 · NIAID · UNIVERSITY OF ROCHESTER · PI MARTINEZ-SOBRIDO, LUIS · 2012 to 2013
$154k
NIAID NIH HHS HHSN266200700008CNIAID NIH HHS R03 AI099681NIAID NIH HHS T32 AI007285NIAID NIH HHS T32 AI 007285-26NINR NIH HHS R21 NR010511PHS HHS HHSN266200700008C
6 · The paper itself

Abstract

Avian-derived influenza A zoonoses are closely monitored and may be an indication of virus strains with pandemic potential. Both successful vaccination and convalescence of influenza A virus in humans typically results in the induction of antibodies that can neutralize viral infection. To improve long-standing and new-generation methodologies for detection of neutralizing antibodies, we have employed a novel reporter-based approach that allows for multiple antigenic testing within a single sample. Central to this approach is a single-cycle infectious influenza A virus (sciIAV), where a functional hemagglutinin (HA) gene was changed to encode either the green or the monomeric red fluorescent protein (GFP and mRFP, respectively) and HA is complemented in trans by stable HA-expressing cell lines. By using fluorescent proteins with non-overlapping emission spectra, this novel bivalent fluorescence-based microneutralization assay (BiFMA) can be used to detect neutralizing antibodies against two distinct influenza isolates in a single reaction, doubling the speed of experimentation while halving the amount of sera required. Moreover, this approach can be used for the rapid identification of influenza broadly neutralizing antibodies. Importantly, this novel BiFMA can be used for any given influenza HA-pseudotyped virus under BSL-2 facilities, including highly pathogenic influenza HA isolates.

Indexed as

Antibodies, NeutralizingFluorometryHemagglutinin Glycoproteins, Influenza VirusHumansInfluenza A virusLuminescent ProteinsNeutralization TestsAntibodies, NeutralizingHemagglutinin Glycoproteins, Influenza VirusLuminescent ProteinsBivalent fluorescence-based microneutralization assay (BiFMA)Green fluorescent protein (GFP)Hemagglutination inhibition (HAI)Hemagglutinin (HA)Monomeric red fluorescent protein (mRFP)Neutralizing antibody (NAb)Single-cycle infectious influenza A virus (sciIAV)Virus neutralization (VN)

Identifiers

PMID26044496
PMCPMC4480155

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.