# Two-Hour Post-dose (C2)-Monitored Cyclosporine Microemulsion as a Practical Alternative to Voclosporin in Mixed Class IV/V Lupus Nephritis: A Case Report

**Authors:** Divya Akella, Virin Ramoutar

PMC · DOI: 10.7759/cureus.102585 · Cureus · 2026-01-29

## TL;DR

A patient with lupus nephritis achieved kidney function improvement using cyclosporine microemulsion monitored at two hours after dose, offering a practical alternative to voclosporin.

## Contribution

Demonstrates the effectiveness of C2-monitored cyclosporine microemulsion as a viable alternative to voclosporin in lupus nephritis treatment.

## Key findings

- Transition to C2-guided cyclosporine microemulsion led to complete proteinuric remission.
- Kidney function remained stable during follow-up with this treatment approach.
- The regimen provided benefits similar to voclosporin with reduced toxicity.

## Abstract

Lupus nephritis (LN) is a major cause of chronic kidney disease and progression to end-stage kidney disease in patients with systemic lupus erythematosus. Calcineurin inhibitor-based therapy is used in LN management because of its combined systemic immunomodulatory effects on T-cell activation and direct podocyte-stabilizing actions, leading to reduction in proteinuria. We report a patient with mixed class IV and V LN who achieved partial remission with voclosporin but was unable to continue therapy. Transition to cyclosporine microemulsion (CsA-ME) guided by two-hour post-dose (C2) monitoring was associated with complete proteinuric remission and stable kidney function during follow-up. This case demonstrates that individualized C2-guided CsA-ME dosing was associated with marked proteinuria reduction and preservation of kidney function. The observed response suggests pharmacodynamic effects that may overlap with those reported for voclosporin, within a fully oral, non-depletive regimen selected to mitigate treatment-related toxicity from cytotoxic therapy after shared decision-making with the patient.

## Linked entities

- **Chemicals:** cyclosporine (PubChem CID 5284373), voclosporin (PubChem CID 6918486)
- **Diseases:** lupus nephritis (MONDO:0005556), systemic lupus erythematosus (MONDO:0007915), chronic kidney disease (MONDO:0005300), end-stage kidney disease (MONDO:0004375)

## Full-text entities

- **Genes:** SYNPO (synaptopodin) [NCBI Gene 11346] {aka SYNPO1}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, CTSL (cathepsin L) [NCBI Gene 1514] {aka CATL, CTSL1, MEP}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, C3 (complement C3) [NCBI Gene 718] {aka AHUS5, ARMD9, ASP, C3a, C3b, CPAMD1}, RNPC3 (RNA binding region (RNP1, RRM) containing 3) [NCBI Gene 55599] {aka CPHD7, IGHD5, RBM40, RNP, SNRNP65}, TRPC6 (transient receptor potential cation channel subfamily C member 6) [NCBI Gene 7225] {aka FSGS2, TRP6}
- **Diseases:** hypertension (MESH:D006973), cytotoxic (MESH:D064420), organ toxicity (MESH:D019965), infection (MESH:D007239), end-stage kidney disease (MESH:D007676), marrow suppression (MESH:D001855), infertility (MESH:D007246), IV (MESH:D006011), Kidney Disease (MESH:D007674), immune dysregulation (OMIM:614878), proliferative (class III/IV) and membranous (class V) disease (MESH:D008313), nephrotic (MESH:D009404), fibrosis (MESH:D005355), prediabetes (MESH:D011236), chronic kidney disease (MESH:D051436), edema (MESH:D004487), atrophy (MESH:D001284), kidney failure (MESH:D051437), CNIs (MESH:D054179), urothelial toxicity (MESH:D014526), LN (MESH:D008181), malignancy (MESH:D009369), tubular injury (MESH:D000230), hypogammaglobulinemia (MESH:D000361), systemic lupus erythematosus (MESH:D008180), Segmental glomerulosclerosis (MESH:C538457), proteinuria (MESH:D011507)
- **Chemicals:** tacrolimus (MESH:D016559), hydroxychloroquine (MESH:D006886), Cyclosporine (MESH:D016572), CsA-ME (-), Rituximab (MESH:D000069283), Prednisone (MESH:D011241), creatinine (MESH:D003404), magnesium (MESH:D008274), calcium (MESH:D002118), mycophenolate (MESH:D009173), losartan (MESH:D019808), Voclosporin (MESH:C484071), empagliflozin (MESH:C570240), blood glucose (MESH:D001786), Cyclophosphamide (MESH:D003520)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## Figures

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949670/full.md

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Source: https://tomesphere.com/paper/PMC12949670