Evidence map›Paper›PMID 35797920›Full record

ReviewCurrent opinion in immunology2022

Harnessing IgG Fc glycosylation for clinical benefit.

Eva J Archer, Joseph C Gonzalez, Debopam Ghosh, Elizabeth D Mellins, Taia T Wang

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Endothelial cells sialylate IgG within the FcRn-mediated recycling pathway.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. 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

5 authors at 1 institution in 1 country.

Eva J ArcherDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.
Joseph C GonzalezDepartment of Medicine, Division of Infectious Diseases, Stanford University School of Medicine, Stanford, CA, USA; Program in Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Debopam GhoshDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA; Program in Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Elizabeth D MellinsDepartment of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA; Program in Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Taia T WangDepartment of Medicine, Division of Infectious Diseases, Stanford University School of Medicine, Stanford, CA, USA; Program in Immunology, Stanford University School of Medicine, Stanford, CA, USA; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Stanford University · US

Funding

COLLABORATIVE INFLUENZA VACCINE INNOVATION CENTER: UNIVERSAL INFLUENZA VACCINE RESEARCH75N93019C00051 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KRAMMER, FLORIAN · 2019 to 2025
$105.4M
MOLECULAR &CELLULAR IMMUNOBIOLOGYT32AI007290 · NIAID · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Olivia M Martinez · 1985 to 2026
$27.0M
Understanding B cell memory in response to diverse virus infectionsU19AI111825 · NIAID · ROCKEFELLER UNIVERSITY · PI BOURNAZOS, STYLIANOS · 2014 to 2023
$26.0M
Regulation of the IgG Fc domain repertoireR01AI139119 · NIAID · STANFORD UNIVERSITY · PI WANG, TAIA · 2019 to 2023
$2.8M
NIAID NIH HHS 75N93019C00051NIAID NIH HHS R01 AI139119NIAID NIH HHS T32 AI007290NIAID NIH HHS U19 AI111825
6 · The paper itself

Abstract

The effector activity of IgG antibodies is regulated at several levels, including IgG subclass, modifications of the Fc glycan, and the distribution of Type I and II Fcγ receptors (FcγR) on effector cells. Here, we explore how Fc glycosylation, particularly sialylation and fucosylation, tunes cellular responses to immune complexes. We review the current understanding of the pathways and mechanisms underlying this biology, address FcγR in antigen presentation, and discuss aspects of the clinical understanding of Fc glycans in therapies and disease.

Indexed as

Immunoglobulin GReceptors, IgGAntigen-Antibody ComplexGlycosylationHumansImmunoglobulin Fc FragmentsPolysaccharidesAntigen-Antibody ComplexImmunoglobulin Fc FragmentsImmunoglobulin GPolysaccharidesReceptors, IgG

Identifiers

PMID35797920
PMCPMC9870045
OpenAlexW4283819230

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.