Abstract

Large vessel vasculitis (LVV), such as giant cell arteritis (GCA) and Takayasu’s arteritis (TA), are autoimmune diseases characterized by granulomatous inflammation of large vessels, including the aorta and its branch vessels. Disease etiology is still unknown. Comparative immunohistochemical (IMH) studies between GCA and TA cases might be important. The purpose of the study was to assess and to compare composition and distribution of the inflammatory infiltrate of the ascending aortic aneurysmal wall. Ascending aortic aneurysm (AAA) tissue blocks belonging to one male patient of 59 years and one female patient aged 36 years, diagnosed with GCA and TA, respectively, were used for histological and IMH analysis. Immunohistochemistry staining was performed using antibodies directed against markers of lymphocytes and macrophages. Histological analysis showed in both cases lymphocytes, macrophages, epithelioid histiocytes and multinucleated giant cells that infiltrate all layers of the arterial wall, intimal hyperplasia and adventitial fibrotic changes of different degrees. Immunohistochemical examination showed that the media and adventitia from GCA aortitis case had increased number of T cells and macrophages compared with TA aortitis case, and a less number of B cells in both. Our study made a morphologic and morphometric analysis of lymphocyte infiltration within aneurysm aortic tissue and demonstrated that immune inflammation is a typical feature of GCA and TA diseases. We also noted the utility of immunohistochemical staining of the aortic biopsies for evaluation of indeterminate or healing GCA and TA cases. Keywords: immunohistochemical, granulomatous inflammation, aortic aneurysm, large vessel vasculitis

Highlights

  • Large vessel vasculitis (LVV), such as giant cell arteritis (GCA) and Takayasu’s arteritis (TA), are autoimmune diseases characterized by granulomatous inflammation of large vessels, including the aorta and its branch vessels

  • Giant cell arteritis and TA are two granulomatous vasculitis which develop on a specific genetic background and share some similarities regarding the immunological pathways involved in their pathogenesis [6]

  • We revealed a significant adventitial reactive fibrosis in the intima, media and adventitia and neovascularization at the medio-adventitial junction in TA [15]. In both TA and GCA we found parietal inflammatory lesions produced in the adventitia through the vasa vasorum, allowing the lymphocytes to gain access to the arterial wall, as Noris M. observed [16]

Read more

Summary

Introduction

Large vessel vasculitis (LVV), such as giant cell arteritis (GCA) and Takayasu’s arteritis (TA), are autoimmune diseases characterized by granulomatous inflammation of large vessels, including the aorta and its branch vessels. In addition it might be initiated in the adventitia, with inflammatory cells entering through the vasa vasorum and subsequently infiltrating into all layers of the aortic wall [9]. The degree of total wall inflammation was evaluated by relating the average inflammatory cell number to the entire studied histological section area.

Objectives
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call