Evidence map›Paper›PMID 38774868›Full record

ArticleFrontiers in immunology2024

Identification of immune subsets with distinct lectin binding signatures using multi-parameter flow cytometry: correlations with disease activity in systemic lupus erythematosus.

Enikő Szabó, Anna Faragó, Gergely Bodor, Nikolett Gémes, László G Puskás, László Kovács, Gábor J Szebeni

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. 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

7 authors.

Enikő SzabóInstitute of Genetics, Laboratory of Functional Genomics, HUN-REN Biological Research Center, Szeged, Hungary.
Anna FaragóAstridbio Technologies Ltd, Szeged, Hungary.
Gergely BodorDepartment of Rheumatology and Immunology, Albert Szent-Gyorgyi Medical School and Health Center, University of Szeged, Szeged, Hungary.
Nikolett GémesInstitute of Genetics, Laboratory of Functional Genomics, HUN-REN Biological Research Center, Szeged, Hungary.
László G PuskásInstitute of Genetics, Laboratory of Functional Genomics, HUN-REN Biological Research Center, Szeged, Hungary.
László Kovács *Department of Rheumatology and Immunology, Albert Szent-Gyorgyi Medical School and Health Center, University of Szeged, Szeged, Hungary.
Gábor J Szebeni *Institute of Genetics, Laboratory of Functional Genomics, HUN-REN Biological Research Center, Szeged, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Cell surface glycosylation can influence protein-protein interactions with particular relevance to changes in core fucosylation and terminal sialylation. Glycans are ligands for immune regulatory lectin families like galectins (Gals) or sialic acid immunoglobulin-like lectins (Siglecs). This study delves into the glycan alterations within immune subsets of systemic lupus erythematosus (SLE). Methods: Evaluation of binding affinities of Galectin-1, Galectin-3, Siglec-1, Results: Elevated AAL, SNA and CD25 Conclusion: Alterations in the glycosylation of immune cells in SLE correlate with disease severity, which might represent potential implications in the pathogenesis of SLE.

Indexed as

Flow CytometryLectinsLupus Erythematosus, SystemicAdultFemaleGalectinsGlycosylationHumansLeukocytes, MononuclearMaleMiddle AgedProtein BindingSeverity of Illness IndexYoung AdultGalectinsLectinsflow cytometryglycobiology of SLEimmunophenotypinglectin bindingsystemic lupus erythematosus

Identifiers

PMID38774868
PMCPMC11106380

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.