Skip to content
2000
Volume 24, Issue 21
  • ISSN: 0929-8673
  • E-ISSN: 1875-533X

Abstract

Atherosclerosis is a chronic vascular disease in which atherosclerotic plaques develop in the arterial wall. It is believed that inflammation plays a major role in atherosclerotic formation and progression. Thus, atherosclerosis can be considered as an inflammatory disease of the arterial vessel. Mouse model demonstrated that T and B cell deficiency reduces the atherosclerotic burden in the formation of an atherosclerotic lesion. CD4+ T helper cells (Th), such as Th1 cells known being the major CD4+ T cell subtype found in mouse models of atherogenesis, increase plaque formation caused by oxLDL. IL-17 (also known as IL-17A) was produced by T cells or by a unique subset of T helper cells. IL-17-producing T cells express interferon- gamma (IFN-γ), an important regulator of immune function, which is highly expressed in atherosclerotic lesions, defying their neat characteristics as Th17 cells. Regulation of Th17 signal pathway may play a significant role in the pathogenesis of multiple inflammatory and autoimmune disorders, such as atherosclerosis. In this review, the structural features of IL-17 family and their roles involved in atherosclerosis are described.

Loading

Article metrics loading...

/content/journals/cmc/10.2174/0929867324666170419150614
2017-06-01
2025-05-25
Loading full text...

Full text loading...

/content/journals/cmc/10.2174/0929867324666170419150614
Loading

  • Article Type:
    Research Article
Keyword(s): Atherosclerosis; IL-17; immune function; lipoproteins; mouse model; plaques; Th17 cells
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test