# Telitacicept for systemic lupus erythematosus-associated peripheral neuropathy: a case report

**Authors:** Jinhui Tan, Hai Huang, Linghua Tan, Bo Li, Ximei Wu, Ruonan She, Junjia Luo, Haitao Yang, Haoru Zhang

PMC · DOI: 10.3389/fimmu.2025.1715983 · Frontiers in Immunology · 2026-01-07

## TL;DR

A 37-year-old woman with lupus-related nerve damage improved significantly after treatment with telitacicept, a new drug that may offer a safer alternative to traditional therapies.

## Contribution

First reported use of telitacicept for SLE-associated peripheral neuropathy, showing promising clinical outcomes.

## Key findings

- Telitacicept led to complete resolution of neuropathic symptoms and normalization of inflammatory markers.
- The drug allowed for significant reduction in steroid and MMF use without relapse.
- Follow-up tests showed no nerve abnormalities eight months after treatment initiation.

## Abstract

Peripheral neuropathy (PN) is a challenging manifestation of systemic lupus erythematosus (SLE) with limited evidence-based treatment guidelines. Current standard therapies, including glucocorticoids (GCs) and cyclophosphamide (CYC), are often effective but carry significant risks, such as gonadal toxicity with CYC, which is a major concern for young women. This case report describes the successful use of telitacicept, a novel dual inhibitor of B-lymphocyte stimulator (BLyS) and a proliferation-inducing ligand (APRIL), in a 37-year-old female with SLE-associated PN. The patient had a 17-year history of SLE and lupus nephritis, previously treated with high cumulative doses of CYC (13.2g), GCs, and mycophenolate mofetil (MMF). She developed PN in 2023, confirmed by electromyography showing axonal and demyelinating lesions. Due to her age and fertility concerns, subcutaneous telitacicept (160 mg/week) was added to her ongoing regimen of prednisone (10 mg/day) and MMF. Following telitacicept initiation, the patient’s neuropathic symptoms (numbness and hypoesthesia) completely resolved within months. Inflammatory markers (ESR, hs-CRP) and complement levels normalized, and proteinuria decreased. This clinical improvement allowed for a significant reduction in prednisone to 2.5 mg/day and MMF dosage. A follow-up electromyography eight months later showed no abnormalities. To our knowledge, this is the first report of telitacicept use for SLE-PN. It demonstrates that telitacicept can be a highly effective and steroid-sparing therapy, offering a safer alternative for patients where conventional immunosuppressants like CYC are contraindicated, particularly those of reproductive age. Future studies should explore parallels with immune checkpoint inhibitor (ICI)-related neuropathies.

## Linked entities

- **Chemicals:** cyclophosphamide (PubChem CID 2907), mycophenolate mofetil (PubChem CID 5281078), prednisone (PubChem CID 5865)
- **Diseases:** systemic lupus erythematosus (MONDO:0007915), lupus nephritis (MONDO:0005556), peripheral neuropathy (MONDO:0003620)

## Full-text entities

- **Genes:** TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** gonadal toxicity (MESH:D006058), demyelinating lesions (MESH:D003711), neuropathic symptoms (MESH:D001750), proteinuria (MESH:D011507), neuropathies (MESH:D009422), SLE (MESH:D008180), PN (MESH:D010523), hypoesthesia (MESH:D006987), lupus nephritis (MESH:D008181), Inflammatory (MESH:D007249)
- **Chemicals:** MMF (MESH:D009173), CYC (MESH:D003520), steroid (MESH:D013256), prednisone (MESH:D011241)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12819753/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12819753/full.md

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Source: https://tomesphere.com/paper/PMC12819753