Evidence map›Paper›PMID 41922188›Full record

ReviewZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences2026

[Research progress on the application of telitacicept in rheumatism and autoimmune diseases].

Xue Wang, Yihuai Xu, Guixia Tong, Hongxia Zhang

Abstract readReviewEnglish Abstract
In one paragraph

Review in Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Xue WangDepartment of Nephrology, Children's Hospital Affiliated to Shandong University (Jinan Children's Hospital), Jinan 250022, China. 782920442@qq.com.
Yihuai XuDepartment of Rheumatism and Immunology, Children's Hospital Affiliated to Shandong University (Jinan Children's Hospital), Jinan 250022, China].
Guixia TongDepartment of Rheumatism and Immunology, Children's Hospital Affiliated to Shandong University (Jinan Children's Hospital), Jinan 250022, China].
Hongxia ZhangDepartment of Rheumatism and Immunology, Children's Hospital Affiliated to Shandong University (Jinan Children's Hospital), Jinan 250022, China]. 1036579519@qq.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditional treatment regimens for rheumatism and autoimmune diseases are associated with significant adverse effects, and some patients have a limited response, leading to poor prognosis. Telitacicept, a biologic agent and fusion protein targeting B cell activating factor (BAFF) and a proliferation inducing ligand (APRIL), offers a novel therapeutic strategy for refractory rheumatism and autoimmune diseases. Clinical trials have shown promising efficacy and safety. In systemic lupus erythematosus, telitacicept reduces disease activity and facilitates glucocorticoid sparing, with favorable outcomes also observed in pediatric patients. In Sjögren's syndrome, telitacicept achieves sustained improvement in clinical symptoms and disease activity. In rheumatoid arthritis, telitacicept improves the response rates for the American College of Rheumatology 20% improvement criteria (ACR20) and for the American College of Rheumatology 50% improvement criteria (ACR50) while significantly reducing glucocorticoid requirements. In IgA vasculitis, studies focused on patients with renal involvement, and showed efficacy in reducing proteinuria in both adults and children. In myasthenia gravis, telitacicept reduces disease severity and improves quality of life. Additionally, telitacicept has shown preliminary therapeutic potential in IgG4-related disease and granulomatosis with polyangiitis, warranting further investigation. Existing clinical data indicate a favorable overall safety profile for telitacicept. However, attention should be paid to long-term risks of infection, decreased immunoglobulin levels, potential resistance mechanisms, and its efficacy and safety in special populations. This review summarizes recent research progress on the use of telitacicept in rheumatism and autoimmune diseases, aiming to provide a reference for its clinical application.

Indexed as

Autoimmune DiseasesRecombinant Fusion ProteinsRheumatic DiseasesArthritis, RheumatoidB-Cell Activating FactorHumansSjogren's SyndromeTumor Necrosis Factor Ligand Superfamily Member 13B-Cell Activating FactorRecombinant Fusion ProteinstelitaciceptTumor Necrosis Factor Ligand Superfamily Member 13A proliferation-inducing ligandAutoimmune diseaseB cell activating factorReviewRheumatismTelitacicept

Identifiers

PMID41922188
PMCPMC13154138

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Registered trials

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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.