Evidence map›Paper›PMID 33046650›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Glycomic analysis of host response reveals high mannose as a key mediator of influenza severity.

Daniel W Heindel, Sujeethraj Koppolu, Yue Zhang, Brian Kasper, Lawrence Meche, Christopher A Vaiana, Stephanie J Bissel, Chalise E Carter, Alyson A Kelvin, Mohamed Elaish and 9 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.1field-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

35 citing papers in PubMed, 63 citations in OpenAlex.

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  5. Gene sequencing andJournal of advanced veterinary and animal research · 2025
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  18. Glycoproteome remodeling and organelle-specificProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  19. Article
  20. Article
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

19 authors at 8 institutions in 3 countries.

Daniel W HeindelBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.ORCID 0000-0002-4760-4501
Sujeethraj KoppoluBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.ORCID 0000-0002-8120-961X
Yue ZhangBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.
Brian KasperBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.
Lawrence MecheBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.
Christopher A VaianaBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003.ORCID 0000-0002-2582-4829
Stephanie J BisselDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261.
Chalise E CarterCenter for Vaccines and Immunology, University of Georgia, Athens, GA 30602.
Alyson A KelvinDepartment of Pediatrics, Dalhousie University, Halifax, NS, B3H 4R2, Canada.
Mohamed ElaishDepartment of Cell Biology, University of Alberta, Edmonton, AB, T6G 2R7, Canada.ORCID 0000-0003-3628-5856
Joaquin Lopez-OrozcoHigh Content Analysis Core, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB, T6G 2R7, Canada.ORCID 0000-0003-0454-9757
Bin ZhangDepartment of Genetics and Genomic Sciences, Mount Sinai Center for Transformative Disease Modeling, Icahn Institute of Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Bin ZhouCenter for Genomics & Systems Biology, Department of Biology, New York University, New York, NY 10003.
Tsui-Wen ChouCenter for Genomics & Systems Biology, Department of Biology, New York University, New York, NY 10003.ORCID 0000-0001-6901-4599
Lauren LashuaCenter for Genomics & Systems Biology, Department of Biology, New York University, New York, NY 10003.ORCID 0000-0002-6739-5188
Tom C HobmanDepartment of Cell Biology, University of Alberta, Edmonton, AB, T6G 2R7, Canada.ORCID 0000-0002-5744-3545
Ted M RossCenter for Vaccines and Immunology, University of Georgia, Athens, GA 30602.ORCID 0000-0003-1947-7469
Elodie GhedinCenter for Genomics & Systems Biology, Department of Biology, New York University, New York, NY 10003.ORCID 0000-0002-1515-725X
Lara K MahalBiomedical Research Institute, Department of Chemistry, New York University, New York, NY 10003; lkmahal@ualberta.ca.ORCID 0000-0003-4791-8524
Biomedical Research Institute · USNew York University · USUniversity of Alberta · CAUniversity of Georgia · USCairo University · EGDalhousie University · CAIcahn School of Medicine at Mount Sinai · USUniversity of Pittsburgh · US

Funding

Omics-Based Predictive Modeling of Age-Dependent Outcome to Influenza InfectionU01AI111598 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GHEDIN, ELODIE · 2013 to 2017
$13.3M
NIAID NIH HHS U01 AI111598
6 · The paper itself

Abstract

Influenza virus infections cause a wide variety of outcomes, from mild disease to 3 to 5 million cases of severe illness and ∼290,000 to 645,000 deaths annually worldwide. The molecular mechanisms underlying these disparate outcomes are currently unknown. Glycosylation within the human host plays a critical role in influenza virus biology. However, the impact these modifications have on the severity of influenza disease has not been examined. Herein, we profile the glycomic host responses to influenza virus infection as a function of disease severity using a ferret model and our lectin microarray technology. We identify the glycan epitope high mannose as a marker of influenza virus-induced pathogenesis and severity of disease outcome. Induction of high mannose is dependent upon the unfolded protein response (UPR) pathway, a pathway previously shown to associate with lung damage and severity of influenza virus infection. Also, the mannan-binding lectin (MBL2), an innate immune lectin that negatively impacts influenza outcomes, recognizes influenza virus-infected cells in a high mannose-dependent manner. Together, our data argue that the high mannose motif is an infection-associated molecular pattern on host cells that may guide immune responses leading to the concomitant damage associated with severity.

Indexed as

Host-Pathogen InteractionsA549 CellsAnimalsCarbohydrate MetabolismFemaleFerretsGlycomicsGlycoproteinsGlycosylationHumansInfluenza A Virus, H1N1 SubtypeInfluenza, HumanLungMannoseMannose-Binding LectinX-Box Binding Protein 1GlycoproteinsMannoseMannose-Binding LectinX-Box Binding Protein 1lectin arraylectin microarraymannan binding lectinmannose binding lectinMBL2

Identifiers

PMID33046650
PMCPMC7604487
OpenAlexW3091980496

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.