Evidence map›Paper›PMID 26960182›Full record

ArticleMucosal immunology2016

Enhanced binding of antibodies generated during chronic HIV infection to mucus component MUC16.

Bronwyn Gunn, Jeffrey Schneider, Maryam Shansab, Arangassery Rosemary Bastian, Kelly Fahrbach, Archer Smith, Alison Mahan, Marcus Karim, Anna Licht, Ivan Zvonar and 16 more

Open access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

37 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Passive immunization of the human vagina.Human vaccines & immunotherapeutics · 2022
    Article
  6. Review
  7. Article
  8. Article
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  12. Review
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  14. The Microbiome as a Key Regulator of Female Genital Tract Barrier Function.Frontiers in cellular and infection microbiology · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  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

26 authors at 3 institutions in 2 countries.

Bronwyn Gunn *Ragon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Jeffrey Schneider *Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University 303 E Superior St, Chicago, IL 60611 USA.
Maryam Shansab *Ragon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Arangassery Rosemary BastianDepartment of Biomedical Engineering, Department of Chemistry and Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208 USA.
Kelly FahrbachDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University 303 E Superior St, Chicago, IL 60611 USA.
Archer SmithDepartment of Chemistry, Molecular Biosciences, and the Proteomics Center of Excellence, Northwestern University, 2145 N. Sheridan Road, Evanston, Illinois 60208, USA.
Alison MahanRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Marcus KarimRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Anna LichtRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Ivan ZvonarRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Jacquelynn TedescoRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Meegan AndersonDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University 303 E Superior St, Chicago, IL 60611 USA.
Anais ChapelRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Todd SuscovichRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
David MalaspinaDepartment of Biomedical Engineering, Department of Chemistry and Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208 USA.
Hendrik StreeckMilitary HIV Research Program, Bethesda, MD, 20817.
Bruce D WalkerRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Arthur KimMasschusetts General Hospital, 149 13 Street, Charlestown, MA, 02129.
Georg LauerMasschusetts General Hospital, 149 13 Street, Charlestown, MA, 02129.
Marcus AltfeldRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Shiv PillaiRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Igal SzleiferDepartment of Biomedical Engineering, Department of Chemistry and Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208 USA.
Neil L KelleherDepartment of Chemistry, Molecular Biosciences, and the Proteomics Center of Excellence, Northwestern University, 2145 N. Sheridan Road, Evanston, Illinois 60208, USA.
Patrick F KiserDepartment of Biomedical Engineering, Department of Chemistry and Chemistry of Life Processes Institute, Northwestern University, Evanston, IL 60208 USA.
Thomas J HopeDepartment of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University 303 E Superior St, Chicago, IL 60611 USA.
Galit AlterRagon Institute of MGH, MIT, and Harvard. 400 Technology Square, Cambridge, MA 02139 USA.
Ragon Institute of MGH, MIT and Harvard · USNorthwestern University · USMassachusetts General Hospital · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Virology and Immunology Technology CoreP30AI117943 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Michael E Newcomb · 2015 to 2026
$38.4M
The role of NK cells during acute HCV infection and antiviral therapyU19AI066345 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAUER, GEORG MICHAEL · 2005 to 2014
$8.5M
Demystifying the antiviral activity of the IgG3+ antibody responseR37AI080289 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALTER, GALIT · 2015 to 2022
$5.8M
Harnessing MUC16-IgG Interactions to Enhance HIV Vaccine FunctionR01AI125171 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HOPE, THOMAS · 2016 to 2020
$2.9M
Cervical/Vaginal Mucus and MicrobicidesR33AI094584 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HOPE, THOMAS · 2013 to 2015
$1.4M
NCI NIH HHS P30 CA060553NIAID NIH HHS P30 AI117943NIAID NIH HHS R01 AI125171NIAID NIH HHS R33 AI094584NIAID NIH HHS R37 AI080289NIAID NIH HHS U19 AI066345
6 · The paper itself

Abstract

Transmission of HIV across mucosal barriers accounts for the majority of HIV infections worldwide. Thus, efforts aimed at enhancing protective immunity at these sites are a top priority, including increasing virus-specific antibodies (Abs) and antiviral activity at mucosal sites. Mucin proteins, including the largest cell-associated mucin, mucin 16 (MUC16), help form mucus to provide a physical barrier to incoming pathogens. Here, we describe a natural interaction between Abs and MUC16 that is enhanced in specific disease settings such as chronic HIV infection. Binding to MUC16 was independent of IgG subclass, but strongly associated with shorter Ab glycan profiles, with agalactosylated (G0) Abs demonstrating the highest binding to MUC16. Binding of Abs to epithelial cells was diminished following MUC16 knockdown, and the MUC16 N-linked glycans were critical for binding. Further, agalactosylated VRC01 captured HIV more efficiently in MUC16. These data point to a novel opportunity to enrich Abs at mucosal sites by targeting Abs to MUC16 through changes in Fc glycosylation, potentially blocking viral movement and sequestering the virus far from the epithelial border. Thus, next-generation vaccines or monoclonal therapeutics may enhance protective immunity by tuning Ab glycosylation to promote the enrichment of Abs at mucosal barriers.

Indexed as

Antibody AffinityCA-125 AntigenFemaleGlycosylationHIV-1HIV AntibodiesHIV InfectionsHumansImmunoglobulin Fc FragmentsImmunoglobulin GMembrane ProteinsMucous MembraneMucusProtein BindingVaginaCA-125 AntigenHIV AntibodiesImmunoglobulin Fc FragmentsImmunoglobulin GMembrane ProteinsMUC16 protein, human

Identifiers

PMID26960182
PMCPMC5017893
OpenAlexW2295803553

What OpenQuestion holds

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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.