# Belimumab-induced remission in refractory lupus mesenteric vasculitis: a case report with 49-month follow-up

**Authors:** Wen-jia Gao, Qi-feng Zang, Yan Xu, Yin-shan Zang

PMC · DOI: 10.3389/fimmu.2026.1687299 · Frontiers in Immunology · 2026-03-04

## TL;DR

A 46-year-old woman with severe lupus-related gut inflammation achieved long-term remission using belimumab, a treatment that may help others with similar conditions.

## Contribution

Belimumab induced 49-month remission in refractory lupus mesenteric vasculitis, the longest documented response to date.

## Key findings

- Belimumab led to sustained remission with resolution of symptoms and imaging findings over 49 months.
- Systemic lupus activity markers improved, including reduced anti-dsDNA and increased complement C3 levels.
- Glucocorticoid dosage was successfully tapered without disease relapse.

## Abstract

Lupus mesenteric vasculitis (LMV) is a rare but life-threatening gastrointestinal complication of systemic lupus erythematosus (SLE). Refractory cases pose significant therapeutic challenges due to limited treatment options and cumulative toxicity from long-term immunosuppressant therapy.

A 46-year-old woman with SLE presented with recurrent abdominal pain, diarrhea, and malar rash over a 1-year period. Despite receiving standard immunosuppressive therapies—including glucocorticoids (GCs), cyclophosphamide, mycophenolate mofetil, and tacrolimus—she experienced multiple relapses of LMV between 2015 and 2020, confirmed by abdominal computed tomography showing bowel wall thickening and the characteristic “target sign.” In September 2020, belimumab (600 mg intravenous every 4 weeks) was initiated alongside a reduced-dose GC regimen. Over a 49-month treatment period (34 doses), the patient achieved sustained remission, with complete resolution of abdominal symptoms, normalization of computed tomography findings, stable Systemic Lupus Erythematosus Disease Activity Index scores (0–4), decreasing anti-double-stranded DNA titers (<20 IU/mL), and rising serum complement C3 levels (>0.6 g/L). GC dosage was successfully tapered to 2.5 mg/day without disease relapse.

This case demonstrates belimumab’s efficacy in achieving the longest documented remission (49 months) in refractory LMV, highlighting its potential as a first-line biologic for steroid-dependent gastrointestinal vasculitis.

## Linked entities

- **Chemicals:** cyclophosphamide (PubChem CID 2907), mycophenolate mofetil (PubChem CID 5281078), tacrolimus (PubChem CID 445643)
- **Diseases:** systemic lupus erythematosus (MONDO:0007915)

## Full-text entities

- **Genes:** C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}
- **Diseases:** LMV (MESH:D020945), abdominal pain (MESH:D015746), SLE (MESH:D008180), malar rash (MESH:C000721270), gastrointestinal vasculitis (MESH:D014657), gastrointestinal complication (MESH:D005767), toxicity (MESH:D064420), diarrhea (MESH:D003967)
- **Chemicals:** tacrolimus (MESH:D016559), mycophenolate mofetil (MESH:D009173), steroid (MESH:D013256), cyclophosphamide (MESH:D003520), Belimumab (MESH:C511911)
- **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/PMC12996141/full.md

## References

15 references — full list in the complete paper: https://tomesphere.com/paper/PMC12996141/full.md

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Source: https://tomesphere.com/paper/PMC12996141