4.5 Article

NK1.1- natural killer T cells upregulate interleukin-17 expression in experimental lupus nephritis

期刊

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
卷 320, 期 5, 页码 F772-F788

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00252.2020

关键词

interleukin-17; lupus nephritis; natural killer T cells; NK1.1(-)

资金

  1. National Research Foundation of Korea - Korean Government [2018R1D1A1B07050196]
  2. Korean Society of Nephrology
  3. National Research Foundation of Korea [2018R1D1A1B07050196] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

This study reveals the upregulation of IL-17 in lupus nephritis and the involvement of natural killer T (NKT) cells in its pathogenesis. Activation of NKT cells regulates IL-17-related immune responses, both systemically and in the kidney, primarily through NK1.1(-) NKT cells. IL-17-secreting NK1.1(-) NKT cells could potentially be targeted for the diagnosis and treatment of lupus nephritis.
Interleukin (IL)-17-secreting invariant natural killer T (NKT) cells are involved in several inflammatory diseases. However, their role in lupus nephritis (LN) has not been fully characterized. Samples from patients with LN or glomerulonephritis and healthy controls were obtained, and elevated IL-17(+) NKT cell numbers and IL-17 expression were observed in blood cells and kidneys, respectively, in patients with LN. Comparison of a mouse model of experimental autoimmune LN with the parental strain (NKT-deficient B6.CD1d(-/-) mice) revealed improved proteinuria, disease severity, and histopathology and decreased levels of chemokine (C-X-C motif) ligand 16 and T cell receptor-alpha variable 14 expression. Spleens and kidneys of B6CD1d(-/-) mice also showed downregulation of inflammatory markers and IL-17. In coculture with renal mesangial and NKT cells, inflammatory markers and IL-17 were upregulated following alpha-galactosylceramide treatment and downregulated after treatment with IL-17-blocking antibodies. This was most prominent with killer cell lectin-like receptor subfamily B member 1C (NK1.1)(-) NKT cells. Thus, IL-17 is upregulated in LN. Activation of NKT cells regulates IL-17-related immune responses systemically and in the kidneys, primarily via NK1.1(-) NKT cells. IL-17-secreting NK1.1(-) NKT cells could serve as diagnostic and therapeutic targets for LN. NEW & NOTEWORTHY This study makes a significant contribution to the literature because our results indicate that IL-17 is upregulated in lupus nephritis and that natural killer T (NKT) cells are involved in its pathogenesis. Activation of NKT cells regulates IL-17-related immune responses, both systemically and in the kidney, and this mainly involves NK1.1(-) NKT cells. Furthermore, IL-17-secreting NK1.1(-) NKT cells could serve as a diagnostic and therapeutic target for lupus nephritis.

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