Low-dose interleukin-2 therapy in systemic lupus erythematosus.
Antonio La CavaPublished in: Rheumatology and immunology research (2023)
In systemic lupus erythematosus (SLE), T regulatory cells (T regs ) contribute to the inhibition of autoimmune responses by suppressing self-reactive immune cells. Interleukin (IL)-2 plays an essential role in the generation, function and homeostasis of the T regs and is reduced in SLE. Several clinical studies, including randomized trials, have shown that low-dose IL-2 therapy in SLE patients is safe and effective and can reduce disease manifestations. This review discusses the rationale for the use of low-dose IL-2 therapy in SLE, the clinical responses in patients, and the effects of this therapy on different types of T cells. Considerations are made on the current and future directions of use of low-dose IL-2 regimens in SLE.
Keyphrases
- low dose
- systemic lupus erythematosus
- end stage renal disease
- disease activity
- high dose
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- prognostic factors
- rheumatoid arthritis
- clinical trial
- multiple sclerosis
- stem cells
- mesenchymal stem cells
- transcription factor
- cell death
- current status
- replacement therapy