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Low-dose interleukin-2 therapy in systemic lupus erythematosus
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 cli...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
De Gruyter
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538619/ https://www.ncbi.nlm.nih.gov/pubmed/37781677 http://dx.doi.org/10.2478/rir-2023-0021 |
Sumario: | 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. |
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