# Mechanism of tacrolimus in the treatment of lupus nephritis

**Authors:** Ming Wang, Jing Zhou, Qiyan Niu, Hongyue Wang

PMC · DOI: 10.3389/fphar.2024.1331800 · Frontiers in Pharmacology · 2024-05-07

## TL;DR

This paper reviews how tacrolimus treats lupus nephritis by suppressing the immune system and reducing inflammation, while also highlighting its potential side effects.

## Contribution

The paper provides a comprehensive review of tacrolimus' mechanisms in treating lupus nephritis, emphasizing both immune and non-immune pathways.

## Key findings

- Tacrolimus inhibits T cell activation and cytokine production via calcineurin inhibition.
- It modulates immune cell activity and balances Th1/Th2 and Th17/Treg ratios in lupus nephritis.
- Tacrolimus also affects non-immune mechanisms like actin cytoskeleton and angiotensin II pathways.

## Abstract

Systemic lupus erythematosus (SLE) is a complex autoimmune disorder, with more than half of the patients developing lupus nephritis (LN), which significantly contributes to chronic kidney disease (CKD) and end-stage renal disease (ESRD). The treatment of lupus nephritis has always been challenging. Tacrolimus (TAC), an effective immunosuppressant, has been increasingly used in the treatment of LN in recent years. This review aims to explore the mechanisms of action of tacrolimus in treating LN. Firstly, we briefly introduce the pharmacological properties of tacrolimus, including its role as a calcineurin (CaN) inhibitor, exerting immunosuppressive effects by inhibiting T cell activation and cytokine production. Subsequently, we focus on various other immunomodulatory mechanisms of tacrolimus in LN therapy, including its effects on T cells, B cells, and immune cells in kidney. Particularly, we emphasize tacrolimus’ regulatory effect on inflammatory mediators and its importance in modulating the Th1/Th2 and Th17/Treg balance. Additionally, we review its effects on actin cytoskeleton, angiotensin II (Ang II)-specific vascular contraction, and P-glycoprotein activity, summarizing its impacts on non-immune mechanisms. Finally, we summarize the efficacy and safety of tacrolimus in clinical studies and trials. Although some studies have shown significant efficacy of tacrolimus in treating LN, its safety remains a challenge. We outline the potential adverse reactions of long-term tacrolimus use and provide suggestions on effectively monitoring and managing these adverse reactions in clinical practice. In general, tacrolimus, as a novel immunosuppressant, holds promising prospects for treating LN. Of course, further research is needed to better understand its therapeutic mechanisms and ensure its safety and efficacy in clinical practice.

## Linked entities

- **Proteins:** ppp3ca.S (protein phosphatase 3, catalytic subunit, alpha isozyme S homeolog), Mdr65 (Multi drug resistance 65)
- **Chemicals:** tacrolimus (PubChem CID 445643)
- **Diseases:** systemic lupus erythematosus (MONDO:0007915), lupus nephritis (MONDO:0005556), chronic kidney disease (MONDO:0005300), end-stage renal disease (MONDO:0004375)

## Full-text entities

- **Genes:** ABCB1 (ATP binding cassette subfamily B member 1) [NCBI Gene 5243] {aka ABC20, CD243, CLCS, ENPAT, GP170, MDR1}, AGT (angiotensinogen) [NCBI Gene 183] {aka ANHU, SERPINA8, hFLT1}
- **Diseases:** autoimmune disorder (MESH:D001327), CKD (MESH:D051436), inflammatory (MESH:D007249), ESRD (MESH:D007676), LN (MESH:D008181), SLE (MESH:D008180)
- **Chemicals:** TAC (MESH:D016559)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11106426/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11106426/full.md

## References

107 references — full list in the complete paper: https://tomesphere.com/paper/PMC11106426/full.md

---
Source: https://tomesphere.com/paper/PMC11106426