Evidence map›Paper›PMID 26200652›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2015

Association of systemic lupus erythematosus with decreased immunosuppressive potential of the IgG glycome.

Frano Vučković, Jasminka Krištić, Ivan Gudelj, Maria Teruel, Toma Keser, Marija Pezer, Maja Pučić-Baković, Jerko Štambuk, Irena Trbojević-Akmačić, Clara Barrios and 18 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed, 1 pooled it
17.3field-weighted citation impact, top 1% 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

157 citing papers in PubMed, 1 synthesis or guideline pooled it, 264 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Article
  8. Advances in the lectin pathway in systemic lupus erythematosus: from clinical correlations and mechanisms to targeted interventions.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  9. IgG N-glycosylation in autoimmune diseases.Frontiers in immunology · 2026
    Review
  10. Not all antibodies are created equal: total IgG glycosylation and severity of antibody-mediated rejection in kidney transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2026
    Article
  11. Article
  12. Immunoglobulin GFrontiers in immunology · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

97 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

28 authors at 12 institutions in 7 countries.

Frano VučkovićGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Jasminka KrištićGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Ivan GudeljGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Maria TeruelPfizer-University of Granada-Junta de Andalucia Centre for Genomics and Oncological Research (GENYO), Granada, Spain.
Toma KeserUniversity of Zagreb, Zagreb, Croatia.
Marija PezerGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Maja Pučić-BakovićGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Jerko ŠtambukGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Irena Trbojević-AkmačićGenos Ltd., Glycoscience Research Laboratory, Zagreb, Croatia.
Clara BarriosKing's College London, London, UK, and Hospital del Mar and Institut Mar d'Investigacions Mediques, Barcelona, Spain.
Tamara PavićUniversity of Zagreb, Zagreb, Croatia.
Cristina MenniKing's College London, London, UK.
Youxin WangCapital Medical University, Beijing, China.
Yong ZhouBeijing Tiantan Hospital and Capital Medical University, Beijing, China.
Liufu CuiAffiliated Kailuan General Hospital of Hebei United University, Tangshan, China.
Haicheng SongAffiliated Kailuan General Hospital of Hebei United University, Tangshan, China.
Qiang ZengInternational Medical Center and Chinese People's Liberation Army General Hospital, Beijing, China.
Xiuhua GuoCapital Medical University, Beijing, China.
Bernardo A Pons-EstelSanatorio Parque, Rosario, Argentina.
Paul McKeigueUniversity of Edinburgh, Edinburgh, UK.
Alan Leslie PatrickKavanagh Street Medical Centre, Port of Spain, Trinidad, West Indies.
Olga GornikUniversity of Zagreb, Zagreb, Croatia.
Tim D SpectorKing's College London, London, UK.
Miroslav HarjačekClinical Hospital Center Sestre Milosrdnice, Zagreb, Croatia.
Marta Alarcon-RiquelmePfizer-University of Granada-Junta de Andalucia Centre for Genomics and Oncological Research (GENYO), Granada, Spain, and Oklahoma Medical Research Foundation, Oklahoma City.
Mariam MolokhiaKing's College London, London, UK.
Wei WangCapital Medical University, Beijing, China, and Edith Cowan University, Perth, Western Australia, Australia.
Gordan LaucGenos Ltd., Glycoscience Research Laboratory, and University of Zagreb, Zagreb, Croatia.
Capital Medical University · CNKing's College London · GBScience Research Laboratory · USUniversity of Zagreb · HRGenos (Croatia) · HRNorth China University of Science and Technology · CNCentro Científico Tecnólogico - Rosario · ARChinese People's Liberation Army · CNOklahoma Medical Research Foundation · USPfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ESSisters of Charity Hospital · HRUniversity of Edinburgh · GB

Funding

UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
SequencingP01AI083194 · NIAID · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI KIMBERLY, ROBERT P. · 2009 to 2013
$9.6M
Identification of Susceptibility Genes for SLE of Amerindian Origin in HispanicsRC1AR058621 · NIAMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALARCON-RIQUELME, MARTA E · 2009 to 2010
$1.0M
Fine Mapping and Replication of a Genome-Wide Association Scan for SLE in HispaniR01CA141700 · NCI · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI ALARCON-RIQUELME, MARTA E · 2009 to 2010
$538k
Arthritis Research UK M0600Arthritis Research UK M0651NCATS NIH HHS UL1 TR001417NCI NIH HHS CA-141700NIAID NIH HHS P01 AI083194NIAMS NIH HHS RC1 AR058621NIAMS NIH HHS RC1-AR-058621Wellcome Trust
6 · The paper itself

Abstract

objectiveGlycans attached to the Fc portion of IgG are important modulators of IgG effector functions. Interindividual differences in IgG glycome composition are large and they associate strongly with different inflammatory and autoimmune diseases. IKZF1, HLA-DQ2A/B, and BACH2 genetic loci that affect IgG glycome composition show pleiotropy with systemic lupus erythematosus (SLE), indicating a potentially causative role of aberrant IgG glycosylation in SLE. We undertook this large multicenter case-control study to determine whether SLE is associated with altered IgG glycosylation.

methodsUsing ultra-performance liquid chromatography analysis of released glycans, we analyzed the composition of the IgG glycome in 261 SLE patients and 247 matched controls of Latin American Mestizo origin (the discovery cohort) and in 2 independent replication cohorts of different ethnicity (108 SLE patients and 193 controls from Trinidad, and 106 SLE patients and 105 controls from China).

resultsMultiple statistically significant differences in IgG glycome composition were observed between patients and controls. The most significant changes included decreased galactosylation and sialylation of IgG (which regulate proinflammatory and antiinflammatory actions of IgG) as well as decreased core fucose and increased bisecting N-acetylglucosamine (which affect antibody-dependent cell-mediated cytotoxicity).

conclusionThe IgG glycome in SLE patients is significantly altered in a way that decreases immunosuppressive action of circulating immunoglobulins. The magnitude of observed changes is associated with the intensity of the disease, indicating that aberrant IgG glycome composition or changes in IgG glycosylation may be an important molecular mechanism in SLE.

Indexed as

Genetic Predisposition to DiseaseAdolescentAdultAgedCase-Control StudiesFemaleGlycoproteinsHumansImmunoglobulin GLupus Erythematosus, SystemicMaleMiddle AgedYoung AdultGlycoproteinsglycosylated IgGImmunoglobulin G

Identifiers

PMID26200652
PMCPMC4626261
OpenAlexW2158387380

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.