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Updated: May 5, 2026

Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 26, 2013
Advances in understanding the Th17/Treg balance in systemic lupus erythematosus: implications for treatment and
Yi Liu1, Ling Xiang2, Rui-Juan Cheng3
1Department of Rheumatology and Immunology, The Chengdu Wenjiang District People's Hospital, Chengdu, China.
Abstract:
Systemic lupus erythematosus (SLE) is a chronic autoimmune disorder characterized by a complex and multifactorial pathogenesis. Recent studies have highlighted the critical role of the disrupted balance between T helper 17 (Th17) cells and regulatory T (Treg) cells in disease initiation and progression. Understanding this imbalance has offered a conceptual framework for developing novel targeted interventions. In this review, we focus on emerging therapeutic strategies aimed at restoring the Th17/Treg balance. We place particular emphasis on the mechanisms and clinical implications of biologic agents, such as IL-17 inhibitors, IL-6 receptor antagonists, low-dose IL-2, and mammalian target of rapamycin (mTOR) pathway inhibitors. Additionally, we explore cell-based therapies, including chimeric antigen receptor T-cell (CAR-T) and CAR-Treg approaches. We also outline ongoing challenges and potential future directions for translating these findings into precise, immune-modulating treatments for patients with SLE.
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