Evidence map›Paper›PMID 28874545›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Increasing the breadth and potency of response to the seasonal influenza virus vaccine by immune complex immunization.

Jad Maamary, Taia T Wang, Gene S Tan, Peter Palese, Jeffrey V Ravetch

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
–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

35 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Controlling timing and location in vaccines.Advanced drug delivery reviews · 2020
    Pooled it
  2. Article
  3. Review
  4. Article
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  6. Review
  7. Review
  8. Article
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  10. Article
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  12. Article
  13. Review
  14. Harnessing IgG Fc glycosylation for clinical benefit.Current opinion in immunology · 2022
    Review
  15. Review
  16. Article
  17. A novel mouse strain optimized for chronic human antibody administration.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  18. Review
  19. Review
  20. 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

5 authors.

Jad MaamaryLeonard Wagner Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY 10065.
Taia T WangLeonard Wagner Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY 10065.
Gene S TanDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Peter PaleseDepartment of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Jeffrey V RavetchLeonard Wagner Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, NY 10065; ravetch@rockefeller.edu.ORCID 0000-0003-2024-9041

Funding

Developing, Demonstrating, and Disseminating Innovative Programs to Achieve Translational SuccessUL1TR001866 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY, KRUEGER, JAMES G · 2016 to 2025
$40.6M
Understanding B cell memory in response to diverse virus infectionsU19AI111825 · NIAID · ROCKEFELLER UNIVERSITY · PI RAVETCH, JEFFREY VICTOR · 2014 to 2023
$26.0M
Toward a Universal Influenza Virus VaccineP01AI097092 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI PALESE, PETER · 2012 to 2022
$17.6M
Understanding Human B Cell Responses to Influenza to Improve the Influenza U19AI109946 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RAVETCH, JEFFREY VICTOR · 2014 to 2018
$9.6M
Regulation of the IgG Fc domain repertoireR01AI139119 · NIAID · STANFORD UNIVERSITY · PI WANG, TAIA · 2019 to 2023
$2.8M
Co-engaging CD23 and BCR for enhanced neutralizing antibody responsesK22AI123478 · NIAID · STANFORD UNIVERSITY · PI WANG, TAIA · 2017 to 2018
$269k
NCATS NIH HHS UL1 TR001866NIAID NIH HHS HHSN272201400008CNIAID NIH HHS K22 AI123478NIAID NIH HHS P01 AI097092NIAID NIH HHS R01 AI139119NIAID NIH HHS U19 AI109946NIAID NIH HHS U19 AI111825
6 · The paper itself

Abstract

The main barrier to reduction of morbidity caused by influenza is the absence of a vaccine that elicits broad protection against different virus strains. Studies in preclinical models of influenza virus infections have shown that antibodies alone are sufficient to provide broad protection against divergent virus strains in vivo. Here, we address the challenge of identifying an immunogen that can elicit potent, broadly protective, antiinfluenza antibodies by demonstrating that immune complexes composed of sialylated antihemagglutinin antibodies and seasonal inactivated flu vaccine (TIV) can elicit broadly protective antihemagglutinin antibodies. Further, we found that an Fc-modified, bispecific monoclonal antibody against conserved epitopes of the hemagglutinin can be combined with TIV to elicit broad protection, thus setting the stage for a universal influenza virus vaccine.

Indexed as

AnimalsDogsFemaleHemagglutinin Glycoproteins, Influenza VirusHumansImmunoglobulin GInfluenza A Virus, H5N1 SubtypeInfluenza, HumanInfluenza VaccinesMadin Darby Canine Kidney CellsMice, Inbred C57BLReceptors, IgEHemagglutinin Glycoproteins, Influenza Virushemagglutinin, human influenza A virusImmunoglobulin GInfluenza VaccinesReceptors, IgECD23immune complexsialylated FcTIVuniversal influenza vaccine

Identifiers

PMID28874545
PMCPMC5617290

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.