• 1 January 1985
    • journal article
    • research article
    • Vol. 120  (1) , 99-105
Abstract
The spontaneous occurrence of pulmonary vasculitis in NZB/W mice, a well-characterized autoimmune strain of mice. These mice develop pulmonary vasculitis in an age-related fashion. Mild perivascular and peribronchiolar lymphoid hyperplasia is first seen at 4 mo. of age and progresses into severe hyperplasia by 8 mo. This percedes the development of angiodestructive lesions, which are first noticeable at 10 mo. By 12 mo. of age all mice show multilobe disease characterized by transmural infiltration of the vascular walls by plasma cells, histiocytes and mature lymphocytes. Mitotic figures and necrosis are rare to absent. Vessel lumens are markedly narrowed and obliterated in severe cases, with focal disruption of the limiting elastic membranes. In mice > 10 mo. of age, there is extension of the infiltrate into the interstitium in a manner similar to that of lymphoid interstitial pneumonia. Arteries and veins are equally affected. The cellular infiltrates and pattern of involvement bears similarity to various pulmonary vasculitides in humans. This is the 1st report of spontaneous pulmonary vasculitis in NZB/W mice.