Evidence map›Paper›PMID 29531320›Full record

ArticleScientific reports2018

A Highly Potent and Broadly Neutralizing H1 Influenza-Specific Human Monoclonal Antibody.

Aitor Nogales, Michael S Piepenbrink, Jiong Wang, Sandra Ortega, Madhubanti Basu, Christopher F Fucile, John J Treanor, Alexander F Rosenberg, Martin S Zand, Michael C Keefer and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 68 citations in OpenAlex.

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  16. Engineering recombinantly expressed lectin-based antiviral agents.Frontiers in cellular and infection microbiology · 2022
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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

12 authors at 2 institutions in 1 country.

Aitor NogalesDepartment of Microbiology & Immunology, University of Rochester, Rochester, NY, USA.
Michael S PiepenbrinkInfectious Diseases Division, University of Rochester, Rochester, NY, USA.
Jiong WangDivision of Nephrology, University of Rochester, Rochester, NY, USA.
Sandra OrtegaDepartment of Microbiology & Immunology, University of Rochester, Rochester, NY, USA.
Madhubanti BasuInfectious Diseases Division, University of Rochester, Rochester, NY, USA.
Christopher F FucileDepartment of Microbiology, Informatics Institute, University of Alabama at Birmingham, Birmingham, AL, USA.
John J TreanorInfectious Diseases Division, University of Rochester, Rochester, NY, USA.
Alexander F RosenbergDepartment of Microbiology, Informatics Institute, University of Alabama at Birmingham, Birmingham, AL, USA.
Martin S ZandDivision of Nephrology, University of Rochester, Rochester, NY, USA.
Michael C KeeferInfectious Diseases Division, University of Rochester, Rochester, NY, USA.
Luis Martinez-SobridoDepartment of Microbiology & Immunology, University of Rochester, Rochester, NY, USA. Luis_Martinez@urmc.rochester.edu.
James J KobieInfectious Diseases Division, University of Rochester, Rochester, NY, USA. James_Kobie@urmc.rochester.edu.
University of Rochester · USUniversity of Alabama at Birmingham · US

Funding

The University of Rochester's Clinical and Translational Science InstituteUL1TR002001 · NCATS · UNIVERSITY OF ROCHESTER · PI WILSON, KAREN M., ZAND, MARTIN S · 2016 to 2024
$34.6M
Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
The University of Rochester's Clinical and Translational Science InstituteUL1TR000042 · NCATS · UNIVERSITY OF ROCHESTER · PI BENNETT, NANCY M, KIEBURTZ, KARL D. · 2012 to 2015
$14.4M
Modeling B Cell Vaccine Responses in Transplant RecipientsR01AI069351 · NIAID · UNIVERSITY OF ROCHESTER · PI HYRIEN, OLLIVIER, ZAND, MARTIN S · 2007 to 2016
$3.7M
Modeling Mechanisms of Adjuvanted Influenza Vaccine Induced IgG Repertoire Diversity and Heterosubtypic ImmunityR01AI129518 · NIAID · UNIVERSITY OF ROCHESTER · PI HYRIEN, OLLIVIER, ZAND, MARTIN S · 2017 to 2021
$3.5M
Modeling Immune Desensitization in Renal TransplantationR01AI098112 · NIAID · UNIVERSITY OF ROCHESTER · PI ZAND, MARTIN S · 2012 to 2016
$1.9M
Predictive Modeling of Multidimensional Anti-Influenza IgG RepertoiresR21AI138500 · NIAID · UNIVERSITY OF ROCHESTER · PI ZAND, MARTIN S · 2018 to 2019
$424k
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
NCATS NIH HHS UL1 TR000042NCATS NIH HHS UL1 TR002001NCRR NIH HHS S10 RR027241NIAID NIH HHS P30 AI078498NIAID NIH HHS R01 AI069351NIAID NIH HHS R01 AI098112NIAID NIH HHS R01 AI129518NIAID NIH HHS R21 AI116285NIAID NIH HHS R21 AI138500
6 · The paper itself

Abstract

Influenza's propensity for antigenic drift and shift, and to elicit predominantly strain specific antibodies (Abs) leaves humanity susceptible to waves of new strains with pandemic potential for which limited or no immunity may exist. Subsequently new clinical interventions are needed. To identify hemagglutinin (HA) epitopes that if targeted may confer universally protective humoral immunity, we examined plasmablasts from a subject that was immunized with the seasonal influenza inactivated vaccine, and isolated a human monoclonal Ab (mAb), KPF1. KPF1 has broad and potent neutralizing activity against H1 influenza viruses, and recognized 83% of all H1 isolates tested, including the pandemic 1918 H1. Prophylactically, KPF1 treatment resulted in 100% survival of mice from lethal challenge with multiple H1 influenza strains and when given as late as 72 h after challenge with A/California/04/2009 H1N1, resulted in 80% survival. KPF1 recognizes a novel epitope in the HA globular head, which includes a highly conserved amino acid, between the Ca and Cb antigenic sites. Although recent HA stalk-specific mAbs have broader reactivity, their potency is substantially limited, suggesting that cocktails of broadly reactive and highly potent HA globular head-specific mAbs, like KPF1, may have greater clinical feasibility for the treatment of influenza infections.

Indexed as

AnimalsAntibodies, MonoclonalAntibodies, NeutralizingHumansImmunity, HumoralInfluenza A Virus, H1N1 SubtypeInfluenza VaccinesMiceOrthomyxoviridae InfectionsSpecies SpecificitySurvival RateAntibodies, MonoclonalAntibodies, NeutralizingInfluenza Vaccines

Identifiers

PMID29531320
PMCPMC5847613
OpenAlexW2789756931

What OpenQuestion holds

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LicenceCC BY
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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.