Evidence map›Paper›PMID 30862743›Full record

ArticlemBio2019

Broad and Protective Influenza B Virus Neuraminidase Antibodies in Humans after Vaccination and their Clonal Persistence as Plasma Cells.

Michael S Piepenbrink, Aitor Nogales, Madhubanti Basu, Christopher F Fucile, Jane L Liesveld, Michael C Keefer, Alexander F Rosenberg, Luis Martinez-Sobrido, James J Kobie

Open access · goldAbstract read
In one paragraph

Article in mBio, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 27 citations in OpenAlex.

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  20. The Quest for a Truly Universal Influenza Vaccine.Frontiers in cellular and infection microbiology · 2019
    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

9 authors at 2 institutions in 1 country.

Michael S Piepenbrink *Infectious Diseases Division, University of Rochester, Rochester, New York, USA.
Aitor Nogales *Department of Microbiology & Immunology, University of Rochester, Rochester, New York, USA.
Madhubanti BasuInfectious Diseases Division, University of Rochester, Rochester, New York, USA.
Christopher F FucileInformatics Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Jane L LiesveldDivision of Hematology/Oncology/James P. Wilmot Cancer Institute, University of Rochester, Rochester, New York, USA.
Michael C KeeferInfectious Diseases Division, University of Rochester, Rochester, New York, USA.
Alexander F RosenbergInformatics Institute, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Luis Martinez-SobridoDepartment of Microbiology & Immunology, University of Rochester, Rochester, New York, USA Luis_Martinez@urmc.rochester.edu James_Kobie@urmc.rochester.edu.
James J KobieInfectious Diseases Division, University of Rochester, Rochester, New York, USA Luis_Martinez@urmc.rochester.edu James_Kobie@urmc.rochester.edu.
University of Rochester · USUniversity of Alabama at Birmingham · US

Funding

The Origin and Fate of Human HIV-Specific Plasma Cells Following VaccinationR21AI116285 · NIAID · UNIVERSITY OF ROCHESTER · PI KOBIE, JAMES J · 2015 to 2016
$422k
BIAcore T100 for research and drug discovery in RochesterS10RR027241 · NCRR · UNIVERSITY OF ROCHESTER · PI KIELKOPF, CLARA · 2010 to 2010
$365k
NCRR NIH HHS S10 RR027241NIAID NIH HHS R21 AI116285
6 · The paper itself

Abstract

Although most seasonal inactivated influenza vaccines (IIV) contain neuraminidase (NA), the extent and mechanisms of action of protective human NA-specific humoral responses induced by vaccination are poorly resolved. Due to the propensity of influenza virus for antigenic drift and shift and its tendency to elicit predominantly strain-specific antibodies, humanity remains susceptible to waves of new strains of seasonal viruses and is at risk from viruses with pandemic potential for which limited or no immunity may exist. Here we demonstrate that the use of IIV results in increased levels of influenza B virus (IBV) NA-specific serum antibodies. Detailed analysis of the IBV NA B cell response indicates concurrent expansion of IBV NA-specific peripheral blood plasmablasts 7 days after IIV immunization which express monoclonal antibodies with broad and potent antiviral activity against both IBV Victoria and Yamagata lineages and prophylactic and therapeutic activity in mice. These IBV NA-specific B cell clonal lineages persisted in CD138

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, ViralCross ProtectionDisease Models, AnimalHealthy VolunteersHumansInfluenza B virusInfluenza, HumanInfluenza VaccinesMiceNeuraminidaseOrthomyxoviridae InfectionsPlasma CellsVaccines, InactivatedViral ProteinsAntibodies, MonoclonalAntibodies, ViralInfluenza VaccinesNA protein, influenza B virusNeuraminidaseVaccines, InactivatedViral ProteinsB cell responseshumaninfluenza vaccinesmonoclonal antibodiesneuraminidase

Identifiers

PMID30862743
PMCPMC6414695
OpenAlexW2921588290

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.