Evidence map›Paper›PMID 39055718›Full record

ReviewFrontiers in immunology2024

Protein-A immunoadsorption combined with immunosuppressive treatment in refractory primary Sjögren's syndrome coexisting with NMOSD: a case report and literature review.

Wei Fan, Xuyan Chen, Pingping Xiao, Bo Wei, Yi Zhang, Jinmei Huang, Shufan Wu, Liangjing Lu

Abstract readCase ReportsReview
In one paragraph

Review 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 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

8 authors.

Wei FanDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Xuyan ChenDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Pingping XiaoDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Bo WeiDepartment of Rheumatology, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen University, Xiamen, China.
Yi ZhangDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Jinmei HuangDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Shufan WuDepartment of Rheumatology and Immunology, The Second Affiliated Hospital of Xiamen Medical College, Xiamen, China.
Liangjing LuDepartment of Rheumatology, Ren ji Hosptial, Shanghai Jiaotong University School of Medicine, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of primary Sjögren's syndrome (pSS) coexisting with neuromyelitis optica spectrum disorder (NMOSD) using protein-A immunoadsorption combined with immunosuppressive therapy has rarely been reported. Herein, we present the case of a 35-year-old female diagnosed with pSS concomitant with NMOSD (pSS-NMOSD) who demonstrated a positive response to protein-A immunoadsorption after failing to respond to therapy comprising high-dose intravenous methylprednisolone (IVMP) and intravenous immunoglobulin (IVIG). Within one week of receiving three sessions of immunoadsorption combined with immunosuppressive treatment, the patient's clinical symptoms (blurred vision, paraparesis, and dysfunctional proprioception) significantly improved. Additionally, a rapid decrease in the circulating levels of Aquaporin-4 immunoglobulin G antibodies (AQP4-IgG), immunoglobulin (Ig) A, IgG, IgM, erythrocyte sedimentation rate (ESR), and rheumatoid factor (RF) were observed. Magnetic resonance imaging (MRI) further revealed a significant reduction in the lesions associated with longitudinal extensive transverse myelitis. During the follow-up period, prednisolone was gradually tapered to a maintenance dose of 5-10 mg/day, whereas mycophenolate mofetil (MMF) was maintained at 1.0-1.5 g/day. The patient's condition has remained stable for four years, with no signs of recurrence or progression observed on imaging examination. Therefore, this case suggests that protein A immunoadsorption may represent a potentially effective therapeutic option for patients with pSS-NMOSD who are refractory to conventional treatments.

Indexed as

Immunosuppressive AgentsNeuromyelitis OpticaSjogren's SyndromeAdultAquaporin 4AutoantibodiesCombined Modality TherapyFemaleHumansImmunosorbent TechniquesStaphylococcal Protein ATreatment OutcomeAquaporin 4AutoantibodiesImmunosuppressive AgentsStaphylococcal Protein Acase reportimmunoadsorptionNMOSDSjögren’s syndrometreatment

Identifiers

PMID39055718
PMCPMC11269126

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.