# Telitacicept for refractory AChR-positive generalized myasthenia gravis: a retrospective real-world study

**Authors:** Xi Rong, Xupeng Sun, Li Wang, Meijie Qu, Liwei Jiang, Min Liu

PMC · DOI: 10.3389/fimmu.2026.1752245 · Frontiers in Immunology · 2026-02-09

## TL;DR

Telitacicept shows promise as a safe and effective treatment for patients with refractory AChR-positive generalized myasthenia gravis.

## Contribution

This study provides real-world evidence of telitacicept's efficacy and safety in treating refractory AChR+ gMG.

## Key findings

- Telitacicept significantly improved QMG scores in refractory AChR+ gMG patients.
- Cumulative response rates reached 69.9% for MGFA-PIS and 73.8% for QMG improvement.
- The therapy reduced the need for prednisone and other immunosuppressants.

## Abstract

Treating refractory acetylcholine receptor-positive generalized myasthenia gravis (AChR+ gMG) remains challenging, especially for patients requiring long-term immunosuppressive therapy. Current treatments often lack specificity and pose significant long-term risks, underscoring the need for alternatives. Telitacicept, a novel dual inhibitor of B lymphocyte stimulator (BLyS) and proliferation-inducing ligand (APRIL), offers a promising targeted therapeutic approach. This study aimed to evaluate the efficacy and safety of telitacicept in the treatment of refractory AChR+ generalized myasthenia gravis.

This retrospective study included 42 patients with refractory AChR+ gMG who received telitacicept. The primary outcomes assessed were changes from baseline in Quantitative Myasthenia Gravis (QMG) scores, analyzed using mixed-effects models. Secondary outcomes comprised cumulative response rates, reductions in concomitant immunosuppressive medications, and safety events.

A total of 42 refractory MG patients with MGFA class II–IV were enrolled. Significant improvements were observed in the QMG total score (least-squares [LS] mean change at month 5: -2.24, 95% CI -3.34 to -1.15, p<0.001), with sustained benefits across ocular, limb, and bulbar areas. Cumulative response rates reached 69.9% for MGFA-PIS and 73.8% for QMG improvement (≥3-point reduction) by 6 months. Notable decreases in prednisone (LS mean -10.17 mg/day, p<0.001) and immunosuppressant use were also seen. The therapy demonstrated a promising safety profile.

Telitacicept demonstrated significant efficacy in refractory AChR+ gMG and may reduce dependence on traditional immunosuppressants. These real-world findings support its use as a valuable treatment choice for this challenging patient group.

## Linked entities

- **Chemicals:** prednisone (PubChem CID 5865)
- **Diseases:** myasthenia gravis (MONDO:0009688)

## Full-text entities

- **Genes:** TNFRSF13B (TNF receptor superfamily member 13B) [NCBI Gene 23495] {aka CD267, CVID, CVID2, IGAD2, RYZN, TACI}, AGRN (agrin) [NCBI Gene 375790] {aka AGRIN, CMS8, CMSPPD}, FCGRT (Fc gamma receptor and transporter) [NCBI Gene 2217] {aka FCRN, FcgammaRn, alpha-chain}, TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}, MUSK (muscle associated receptor tyrosine kinase) [NCBI Gene 4593] {aka CMS9, FADS}, LRP4 (LDL receptor related protein 4) [NCBI Gene 4038] {aka CLSS, CMS17, LRP-4, LRP10, MEGF7, SOST2}, CHRNA1 (cholinergic receptor nicotinic alpha 1 subunit) [NCBI Gene 1134] {aka ACHRA, ACHRD, CHRNA, CMS1A, CMS1B, CMS2A}
- **Diseases:** malignancies (MESH:D009369), Sjogren's syndrome (MESH:D012859), bone marrow suppression (MESH:D001855), lymphocytopenia (MESH:D008231), muscle weakness (MESH:D018908), infections (MESH:D007239), osteoporosis (MESH:D010024), hyperglycemia (MESH:D006943), rheumatoid arthritis (MESH:D001172), PE (MESH:D054219), Myasthenia (MESH:D020294), respiratory infections (MESH:D012141), hypertension (MESH:D006973), IgAN (MESH:D005922), NMOSD (MESH:D009471), hyperplasia (MESH:D006965), impaired neuromuscular transmission (MESH:D020511), MGFA class II-IV (MESH:D008312), MG (MESH:D009157), SLE (MESH:D008180), autoimmune disorder (MESH:D001327), thyroid disease (MESH:D013959), Thymic abnormalities (MESH:D013953), liver dysfunction (MESH:D017093), allergic reactions (MESH:D004342), thymoma (MESH:D013945), myopathy (MESH:D009135), fatigue (MESH:D005221)
- **Chemicals:** MMF (MESH:D009173), CYA (MESH:D016572), Tac (MESH:D016559), Prednisone (MESH:D011241), steroid (MESH:D013256), pyridostigmine bromide (MESH:D011729)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## Figures

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## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926135/full.md

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Source: https://tomesphere.com/paper/PMC12926135