4.4 Article

Sheep-Associated Malignant Catarrhal Fever: Role of Latent Virus and Macrophages in Vasculitis

Journal

VETERINARY PATHOLOGY
Volume 58, Issue 2, Pages 332-345

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0300985820978310

Keywords

cattle; malignant catarrhal fever; vasculitis; rete mirabile

Funding

  1. Ministry of Higher Education and Scientific Research in Iraq (MOHESR)

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The study suggests that the vasculitis in MCF originates from the interaction between infected cells and immune cells, leading to infiltration of inflammatory cells and recruitment of white blood cells in the blood vessels, resulting in structural changes in the vasculature. Macrophages and T cells are the main infiltrating cells, capable of proliferating locally, and the process is accompanied by widespread viral infection.
Malignant catarrhal fever (MCF) is a sporadic, generally fatal disease caused by gammaherpesviruses in susceptible dead-end hosts. A key pathological process is systemic vasculitis in which productively infected cytotoxic T cells play a major role. Nonetheless, the pathogenesis of MCF vasculitis is not yet clear. We hypothesized that it develops due to an interaction between virus-infected cells and immune cells, and we undertook a retrospective in situ study on the rete mirabile arteries of confirmed ovine gammaherpesvirus-2 (OvHV-2)-associated MCF cases in cattle, buffalo, and bison. Our results suggest that the arteritis develops from an adventitial infiltration of inflammatory cells from the vasa vasorum, and recruitment of leukocytes from the arterial lumen that leads to a superimposed infiltration of the intima and media that can result in chronic changes including neointimal proliferation. We found macrophages and T cells to be the dominant infiltrating cells, and both could proliferate locally. Using RNA in situ hybridization and immunohistology, we showed that the process is accompanied by widespread viral infection, not only in infiltrating leukocytes but also in vascular endothelial cells, medial smooth muscle cells, and adventitial fibroblasts. Our results suggest that OvHV-2-infected T cells, monocytes, and locally proliferating macrophages contribute to the vasculitis in MCF. The initial trigger or insult that leads to leukocyte recruitment and activation is not yet known, but there is evidence that latently infected, activated endothelial cells play a role in this. Activated macrophages might then release the necessary pro-inflammatory mediators and, eventually, induce the characteristic vascular changes.

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