Evidence map›Paper›PMID 22235365›Full record

ArticleAutoimmune diseases2011

B-cell-activating factor and autoimmune myasthenia gravis.

Samia Ragheb, Robert P Lisak

Open access · goldAbstract read
In one paragraph

Article in Autoimmune diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. A Rare Case of Chronic Lymphocytic Leukemia Complicated by Myasthenia Gravis.Journal of community hospital internal medicine perspectives · 2025
    Article
  3. Review
  4. Novel Immunotherapies for Myasthenia Gravis.ImmunoTargets and therapy · 2023
    Review
  5. Inflammation and autoimmune myasthenia gravis.Frontiers in immunology · 2023
    Review
  6. Review
  7. Novel Treatments in Myasthenia Gravis.Frontiers in neurology · 2020
    Review
  8. Article
  9. Article
  10. Advances in autoimmune myasthenia gravis management.Expert review of neurotherapeutics · 2018
    Review
  11. Article
  12. Current Treatment, Emerging Translational Therapies, and New Therapeutic Targets for Autoimmune Myasthenia Gravis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Review
  13. Article
  14. Myasthenia gravis: an update for the clinician.Clinical and experimental immunology · 2014
    Review
  15. Review
  16. Review
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 at 1 institution in 1 country.

Samia RaghebDepartment of Neurology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Robert P Lisak
Wayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BAFF is a potent B-cell survival factor, and it plays an essential role in B-cell homeostasis and B-cell function in the periphery. Both normal and autoreactive B cells are BAFF dependent; however, excess BAFF promotes the survival, growth, and maturation of autoreactive B cells. When overexpressed, BAFF protects B cells from apoptosis, thereby contributing to autoimmunity. Three independent studies have shown higher BAFF levels in the circulation of MG patients. BAFF may play an important role in the pathogenesis of MG. BAFF antagonists may well provide new treatment options for MG patients, particularly those patients with thymic lymphoid follicular hyperplasia.

Identifiers

PMID22235365
PMCPMC3251912
OpenAlexW2078361288

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.