Evidence map›Paper›PMID 27303031›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

B-cell-independent sialylation of IgG.

Mark B Jones, Douglas M Oswald, Smita Joshi, Sidney W Whiteheart, Ron Orlando, Brian A Cobb

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

91 citing papers in PubMed, 135 citations in OpenAlex.

  1. Trial
  2. Article
  3. Sialylation in the nervous system: Functions and mechanisms.The Journal of biological chemistry · 2026
    Review
  4. Immunoglobulin G in aging and cancer.Frontiers in immunology · 2026
    Review
  5. Article
  6. 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
  7. Review
  8. Therapeutic effect of galactosyltransferase- and sialyltransferase-encoding mRNA in rheumatoid arthritis.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  9. Article
  10. Article
  11. Role of Antibody Glycosylation in Health, Disease, and Therapy.Handbook of experimental pharmacology · 2025
    Review
  12. Review
  13. B Cell Responses to the Placenta and Fetus.Annual review of pathology · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Antigen specificity shapes antibody functions in tuberculosis.bioRxiv : the preprint server for biology · 2024
    Article
  19. Article
  20. Review

31 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 1 country.

Mark B JonesDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106;
Douglas M OswaldDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106;
Smita JoshiDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536;
Sidney W WhiteheartDepartment of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40536;
Ron OrlandoComplex Carbohydrate Research Center, University of Georgia, Athens, GA 30602; Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602.
Brian A CobbDepartment of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106; brian.cobb@case.edu.
University of Kentucky · USUniversity School · USCase Western Reserve University · USUniversity of Georgia · US

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SASISEKHARAN, RAM · 2001 to 2010
$80.3M
MOLECULAR MECHANISMS OF PLATELET EXOCYTOSISR01HL056652 · NHLBI · UNIVERSITY OF KENTUCKY · PI WHITEHEART, SIDNEY WALDO · 1996 to 2019
$5.2M
TRAINING IN GEOGRAPHIC MEDICINE &INFECTIOUS DISEASET32AI007024 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI KAZURA, JAMES WALTER · 1985 to 2020
$4.5M
Immunology Training Program-PredoctoralT32AI089474 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI COBB, BRIAN A · 2010 to 2025
$3.4M
Protein-Glycan Interaction Resource of the CFGR24GM098791 · NIGMS · EMORY UNIVERSITY · PI CUMMINGS, RICHARD D, PAULSON, JAMES C · 2011 to 2013
$2.6M
Antigenic Carbohydrate Structure, Function, and SpecificityR01GM082916 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI COBB, BRIAN A · 2009 to 2016
$1.9M
T cell Dependent Immune Responses to Carbohydrate AntigensDP2OD004225 · OD · CASE WESTERN RESERVE UNIVERSITY · PI COBB, BRIAN A · 2008 to 2008
$1.9M
Connecting the microbiota to peripheral immune quiescence by T cell crosstalkF32AI114109 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI JONES, MARK B · 2015 to 2017
$124k
NHLBI NIH HHS R01 HL056652NIAID NIH HHS F32 AI114109NIAID NIH HHS T32 AI007024NIAID NIH HHS T32 AI089474NIGMS NIH HHS R01 GM082916NIGMS NIH HHS R24 GM098791NIGMS NIH HHS U54 GM062116NIH HHS DP2 OD004225
6 · The paper itself

Abstract

IgG carrying terminal α2,6-linked sialic acids added to conserved N-glycans within the Fc domain by the sialyltransferase ST6Gal1 accounts for the anti-inflammatory effects of large-dose i.v. Ig (IVIg) in autoimmunity. Here, B-cell-specific ablation of ST6Gal1 in mice revealed that IgG sialylation can occur in the extracellular environment of the bloodstream independently of the B-cell secretory pathway. We also discovered that secreted ST6Gal1 is produced by cells lining central veins in the liver and that IgG sialylation is powered by serum-localized nucleotide sugar donor CMP-sialic acid that is at least partially derived from degranulating platelets. Thus, antibody-secreting cells do not exclusively control the sialylation-dependent anti-inflammatory function of IgG. Rather, IgG sialylation can be regulated by the liver and platelets through the corresponding release of enzyme and sugar donor into the cardiovascular circulation.

Indexed as

Animalsbeta-D-Galactoside alpha 2-6-SialyltransferaseBlood PlateletsB-LymphocytesImmunoglobulin GLiverMice, KnockoutOvalbuminPolysaccharidesProtein Processing, Post-TranslationalSialic AcidsSialyltransferasesbeta-D-Galactoside alpha 2-6-SialyltransferaseImmunoglobulin GOvalbuminPolysaccharidesSialic AcidsSialyltransferasesB cellIgGIVIgsialylationsialyltransferase

Identifiers

PMID27303031
PMCPMC4932940
OpenAlexW2421962974

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.