# Case Report: Telitacicept in the treatment of cSLE-APS: novel therapeutic perspectives on autoimmune thrombotic diseases in children

**Authors:** Jingyue Liu, Zhilang Cao, Yajun Wang, Jing Zheng

PMC · DOI: 10.3389/fimmu.2025.1675554 · Frontiers in Immunology · 2026-02-06

## TL;DR

This case report shows that telitacicept can effectively treat a severe autoimmune condition in children, offering new hope for managing related diseases.

## Contribution

The first reported case of telitacicept-induced remission in cSLE-APS, highlighting its novel dual inhibition of BAFF/APRIL.

## Key findings

- Telitacicept resolved life-threatening infarctions in a cSLE-APS patient.
- Corticosteroids were successfully discontinued within six months of treatment.
- LLDAS was maintained, indicating effective disease control.

## Abstract

Thrombotic antiphospholipid syndrome (APS) in Childhood-onset systemic lupus erythematosus (cSLE) remains a therapeutic frontier. Here, we report the first case of telitacicept (a TACI-Fc fusion protein)- induced remission in cSLE related antiphospholipid syndrome (cSLE-APS), where targeted dual BAFF(B cell-activating factor)/APRIL(a proliferation-inducing ligand) inhibition resolved life-threatening infarctions and achieved sustained disease control. During treatment, corticosteroids were successfully discontinued within six months, and a lupus low disease activity state (LLDAS) was maintained. Our findings indicate that telitacicept’s unique ability to regulate B-cell activity could target the dual pathology of cSLE-APS, offering a new therapeutic approach for this serious condition.

## Linked entities

- **Proteins:** TNFSF13B (TNF superfamily member 13b), TNFSF13 (TNF superfamily member 13)
- **Diseases:** antiphospholipid syndrome (MONDO:0017278)

## Full-text entities

- **Genes:** TNFRSF13B (TNF receptor superfamily member 13B) [NCBI Gene 23495] {aka CD267, CVID, CVID2, IGAD2, RYZN, TACI}, BTG3 (BTG anti-proliferation factor 3) [NCBI Gene 10950] {aka ANA, ANA/BTG3, APRO4, TOB5, TOB55, TOFA}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TNFSF13B (TNF superfamily member 13b) [NCBI Gene 10673] {aka BAFF, BLYS, CD257, TALL-1, TALL1, THANK}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, MB (myoglobin) [NCBI Gene 4151] {aka MYOSB, PVALB}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}
- **Diseases:** pulmonary artery dilation (MESH:D000071079), cough (MESH:D003371), Antiphospholipid antibodies (MESH:D016736), leukocytosis (MESH:D007964), swelling (MESH:D004487), dizziness (MESH:D004244), renal, neurological, and hematological involvement (MESH:C565423), myocardial infarction (MESH:D009203), psychiatric (MESH:D001523), Infection (MESH:D007239), neuropsychiatric involvement (MESH:C000631768), thrombocytopenia (MESH:D013921), immune (MESH:D007154), ischemic lesions (MESH:D017202), ischemic (MESH:D002545), cerebral infarcts (MESH:D002544), encephalopathy (MESH:D001927), pain (MESH:D010146), cytopenias (MESH:D006402), encephalomalacia (MESH:D004678), aCL (MESH:D007153), MINOCA (MESH:D000088442), anemia (MESH:D000740), LA (MESH:C531622), AIHA (MESH:D000744), inflammatory (MESH:D007249), atrial appendage thrombus (MESH:D013927), damage (MESH:D020263), regurgitation (MESH:D008944), pericardial effusion (MESH:D010490), Lupus Erythematosus Disease (MESH:D008180), LLPCs (MESH:D007952), erythema (MESH:D004890), fever (MESH:D005334), gait instability (MESH:D043171), thromboembolic (MESH:D013923), fatigue (MESH:D005221), myocardial injury (MESH:D009202), jaundice (MESH:D007565), LLDAS (MESH:D009800), NYHA (MESH:D006331), left (MESH:D018487), infarctions (MESH:D007238), heart failure (MESH:D006333), autoimmune disorder (MESH:D001327), hypogammaglobulinemia (MESH:D000361), Nephropathy (MESH:D007674)
- **Chemicals:** Rituximab (MESH:D000069283), HCQ (MESH:D006886), antiphospholipid (-), MMF (MESH:D009173), clopidogrel bisulfate (MESH:D000077144), Belimumab (MESH:C511911), calcium (MESH:D002118), warfarin (MESH:D014859), Digoxin (MESH:D004077), phospholipid (MESH:D010743), Spironolactone (MESH:D013148), Prednisone (MESH:D011241), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12920562/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920562/full.md

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Source: https://tomesphere.com/paper/PMC12920562