Evidence map›Paper›PMID 29672582›Full record

ArticlePloS one2018

Changes in N-glycans of IgG4 and its relationship with the existence of hypocomplementemia and individual organ involvement in patients with IgG4-related disease.

Naoki Konno, Mitsuru Sugimoto, Tadayuki Takagi, Makiko Furuya, Tomoyuki Asano, Shuzo Sato, Hiroko Kobayashi, Kiyoshi Migita, Yoshiaki Miura, Taichi Aihara and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 12% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. 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

13 authors at 2 institutions in 1 country.

Naoki KonnoDepartment of Gastroenterology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Mitsuru SugimotoDepartment of Gastroenterology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Tadayuki TakagiDepartment of Gastroenterology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Makiko FuruyaDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Tomoyuki AsanoDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Shuzo SatoDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Hiroko KobayashiDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Kiyoshi MigitaDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Yoshiaki MiuraS-Bio, Sumitomo Bakelite Co., Ltd., Hudson, New Hampshire, United States of America.ORCID 0000-0001-5806-2712
Taichi AiharaS-Bio, Sumitomo Bakelite Co., Ltd., Hudson, New Hampshire, United States of America.
Atsushi KomatsudaDepartment of Hematology, Nephrology, and Rheumatology, School of Medicine, Akita University, Akita, Japan.ORCID 0000-0003-1477-8131
Hiromasa OhiraDepartment of Gastroenterology, School of Medicine, Fukushima Medical University, Fukushima, Japan.
Hiroshi WatanabeDepartment of Rheumatology, School of Medicine, Fukushima Medical University, Fukushima, Japan.ORCID 0000-0002-1333-4806
Fukushima Medical University · JPAkita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough increased serum IgG4 level and tissue infiltration of IgG4-positive cells are key events in IgG4-related disease (IgG4RD), and nearly half of IgG4RD patients show hypocomplementemia, the role of IgG4 in the pathogenesis of IgG4RD remains unclear. Many reports show that altered IgG glycosylation, especially IgG with agalactosylated N-linked glycan (G0 N-glycan), have proinflammatory roles including complement activation, implicated in the pathogenesis of various inflammatory diseases. This study determined the concentration of N-linked glycans (N-glycan) released from serum IgG4 in IgG4RD patients and compared the difference of glycosylation changes to those in healthy controls. We also compared the concentration of each IgG4 glycoform between patients with and without hypocomplementemia and individual organ involvement (kidney, pancreas, lymph node) in IgG4RD.

methodsWe collected sera from 12 IgG4RD patients and 8 healthy controls. IgG4 was isolated from sera via Melon™ Gel IgG Spin Purification Kit followed by Capture Select IgG4 (Hu) Affinity Matrix. IgG4 N-glycans were analyzed by S-BIO GlycanMap® Xpress methodology.

resultsSignificant increases of IgG4 G0 N-glycan and IgG4 fucosylated N-glycan (F1 N-glycan) concentrations were observed in IgG4RD compared with healthy controls. Although we observed decreased levels of IgG4 F0 glycan in IgG4RD with hypocomplementemia, there were no significant differences in the galactosylation and sialyation of IgG4 N-glycans. Furthermore, there were no significant differences in the glycosylation of IgG4 N-glycans between patients with and without individual organ involvement of IgG4RD.

conclusionsAlthough IgG4 has anti-inflammatory properties, IgG4 G0 and F1 glycans were increased in patients with IgG4RD. Our results suggest that decreased galactosylation of IgG4 is not related to complement activation and the differences of individual organ involvement in IgG4RD. IgG4 fucosylation change may be related to complement activation in IgG4RD. Further investigation is needed to clarify the role of IgG4 in IgG4RD.

Indexed as

AgedCase-Control StudiesComplement System ProteinsFemaleGlycoproteinsGlycosylationHumansImmune System DiseasesImmunoglobulin GMaleMiddle AgedPolysaccharidesComplement System ProteinsGlycoproteinsglycosylated IgGImmunoglobulin GPolysaccharides

Identifiers

PMID29672582
PMCPMC5908088
OpenAlexW2801380723

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.