Evidence map›Paper›PMID 31748388›Full record

ArticleJournal of virology2020

Broadly Inhibiting Antineuraminidase Monoclonal Antibodies Induced by Trivalent Influenza Vaccine and H7N9 Infection in Humans.

Pramila Rijal, Bei Bei Wang, Tiong Kit Tan, Lisa Schimanski, Philipp Janesch, Tao Dong, John W McCauley, Rodney S Daniels, Alain R Townsend, Kuan-Ying A Huang

Open access · hybridAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

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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

10 authors at 6 institutions in 3 countries.

Pramila Rijal *Center for Translational Immunology, Chinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom Pramila.rijal@rdm.ox.ac.uk arthur1726@cgmh.org.tw.
Bei Bei Wang *Institute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Tiong Kit TanMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Lisa SchimanskiMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Philipp JaneschMRC Human Immunology Unit, MRC Weatherall Institute of Molecular Medicine, Radcliffe Department of Medicine, University of Oxford, Oxford, United Kingdom.
Tao DongCenter for Translational Immunology, Chinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
John W McCauleyWorldwide Influenza Centre, The Francis Crick Institute, London, United Kingdom.
Rodney S DanielsWorldwide Influenza Centre, The Francis Crick Institute, London, United Kingdom.
Alain R TownsendCenter for Translational Immunology, Chinese Academy of Medical Sciences Oxford Institute, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Kuan-Ying A HuangDivision of Infectious Diseases, Department of Paediatrics, Chang Gung Memorial Hospital, Taoyuan, Taiwan Pramila.rijal@rdm.ox.ac.uk arthur1726@cgmh.org.tw.
University of Oxford · GBMRC Human Immunology Unit · GBThe Francis Crick Institute · GBAcademy of Medical Sciences · GBBeijing Ditan Hospital · CNChang Gung Memorial Hospital · TW

Funding

Cancer Research UK FC001030Medical Research Council FC001030Medical Research Council MC_UU_00008/11Medical Research Council MR/L018942/1Medical Research Council MR/P021336/1Wellcome Trust FC001030
6 · The paper itself

Abstract

The majority of antibodies induced by influenza neuraminidase (NA), like those against hemagglutinin (HA), are relatively specific to viruses isolated within a limited time window, as seen in serological studies and the analysis of many murine monoclonal antibodies (MAbs). We report three broadly reactive human MAbs targeting N1 NA. Two were isolated from a young adult vaccinated with trivalent influenza vaccine (TIV), which inhibited N1 NA from viruses isolated from humans over a period of a hundred years. The third antibody, isolated from a child with acute mild H7N9 infection, inhibited both group 1 N1 and group 2 N9 NAs. In addition, the antibodies cross-inhibited the N1 NAs of highly pathogenic avian H5N1 influenza viruses. These antibodies are protective in prophylaxis against seasonal H1N1 viruses in mice. This study demonstrates that human antibodies to N1 NA with exceptional cross-reactivity can be recalled by vaccination and highlights the importance of standardizing the NA antigen in seasonal vaccines to offer optimal protection.

Indexed as

AnimalsAntibodies, MonoclonalChildCross ProtectionCross ReactionsDogsFemaleHEK293 CellsHemagglutininsHumansImmunization, PassiveInfluenza A Virus, H1N1 SubtypeInfluenza A Virus, H5N1 SubtypeInfluenza A Virus, H7N9 SubtypeInfluenza, HumanInfluenza VaccinesAntibodies, MonoclonalHemagglutininsInfluenza VaccinesNeuraminidaseELLAH7N9 virusimmune responseimmunizationinfluenza neuraminidaseinfluenza virusmonoclonal antibodies

Identifiers

PMID31748388
PMCPMC6997757
OpenAlexW2984052607

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.