Evidence map›Paper›PMID 40149905›Full record

ReviewBiomolecules2025

IgG Biomarkers in Multiple Sclerosis: Deciphering Their Puzzling Protein A Connection.

Leonard Apeltsin, Xiaoli Yu

Abstract readReview
In one paragraph

Review in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. 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

2 authors.

Leonard ApeltsinAnomaly Insights, 500 7th Ave, Floor 8, New York, NY 10028, USA.
Xiaoli YuDepartment of Neurosurgery, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0003-4850-8586

Funding

Development of Validation of Phage-Displayed Random Peptide Libraries Technologies for Rapid Isolation and Characterization of Extracellular Vesicles from Patients with Brain TumorsR33MH118174 · NIMH · UNIVERSITY OF COLORADO DENVER · PI GRANER, MICHAEL W., YU, XIAOLI · 2020 to 2022
$1.9M
NIMH NIH HHS R33 MH118174United States Department of Defense HT94252410815University of Colorado Chancelor's Innovation Award na
6 · The paper itself

Abstract

Identifying reliable biomarkers in peripheral blood is critical for advancing the diagnosis and management of multiple sclerosis (MS), particularly given the invasive nature of cerebrospinal fluid (CSF) sampling. This review explores the role of B cells and immunoglobulins (Igs), particularly IgG and IgM, as biomarkers for MS. B cell oligoclonal bands (OCBs) in the CSF are well-established diagnostic tools, yet peripheral biomarkers remain underdeveloped. Emerging evidence highlights structural and functional variations in immunoglobulin that may correlate with disease activity and progression. A recent novel discovery of blood IgG aggregates in MS patients that fail to bind Protein A reveals promising diagnostic potential and confirms previous findings of the unique features of immunoglobulin G in MS and the potential link between the superantigen Protein A and MS. These aggregates, enriched in IgG1 and IgG3 subclasses, exhibit unique structural properties, including mutations in the framework region 3 (FR3) of

Indexed as

Immunoglobulin GMultiple SclerosisBiomarkersB-LymphocytesHumansBiomarkersImmunoglobulin GB cellsblood biomarkerCDRcomplementarity determining regiondiagnosisFc gamma receptorframeworkIgGIgG1IgG3IgG aggregatesIGHV3IGHV4IgMimmunoglobulinmultiple sclerosisoligoclonal bandprotein A

Identifiers

PMID40149905
PMCPMC11940459

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.