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Updated: Nov 16, 2025

Isolation and Th17 Differentiation of Naïve CD4 T Lymphocytes
Published on: September 26, 2013
Interleukin-17A Interweaves the Skeletal and Immune Systems
Mengjia Tang1, Lingyun Lu2, Xijie Yu1
1Department of Endocrinology and Metabolism, Laboratory of Endocrinology and Metabolism, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, China.
Interleukin-17A (IL-17A) is a key cytokine influencing bone health. This review explores IL-17A's dual role in bone metabolism and its implications for immune-mediated bone diseases.
Area of Science:
- Immunology
- Skeletal Biology
- Rheumatology
Background:
- The immune and skeletal systems exhibit complex crosstalk crucial for maintaining bone homeostasis.
- Interleukin-17A (IL-17A), produced by immune cells like Th17 cells, is a significant cytokine involved in this interaction.
Purpose of the Study:
- To review the pathophysiological roles of IL-17A in skeletal homeostasis.
- To discuss the potential therapeutic strategies targeting IL-17A in immune-mediated bone diseases.
Main Methods:
- Literature review summarizing existing research on IL-17A and bone metabolism.
- Analysis of IL-17A's effects on osteoclasts and osteoblasts.
- Examination of IL-17A's involvement in various immune-mediated bone diseases.
Main Results:
- IL-17A exerts direct and indirect effects on osteoclasts, with a dual role influenced by concentration and interacting factors.
- IL-17A also demonstrates a dual role in osteoblasts in vitro.
- IL-17A is implicated as a bone-destructive cytokine in conditions such as postmenopausal osteoporosis, rheumatoid arthritis, psoriatic arthritis, and axial spondylarthritis.
Conclusions:
- IL-17A plays a critical, often detrimental, role in the pathogenesis of immune-mediated bone diseases.
- Understanding IL-17A's complex actions provides avenues for developing targeted therapies for skeletal disorders.
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