H. Mizutani et al., GASTROINTESTINAL VASCULITIS IN AUTOIMMUNE-PRONE (NZWXBXSB)F-1 MICE - ASSOCIATION WITH ANTICARDIOLIPIN AUTOANTIBODIES, Proceedings of the Society for Experimental Biology and Medicine, 209(3), 1995, pp. 279-285
Gastrointestinal vasculitis is a fatal aspect of systemic lupus erythe
matosus. Whether lupus-prone strains of mice develop gastrointestinal
vasculitis, and whether it is accompanied by elevated titres of antica
rdiolipin autoantibody is not known. Lupus-prone (NZW 10 BXSB)F-1 (W/B
F1) mice, and other strains were examined immunohistologically. Levels
of anticardiolipin autoantibody and circulating immune complexes were
determined by microELISA. Reciprocal haploidentical marrow transplant
ations between W/BF1 and autoimmune-resistent B6C3F(1) mice were made.
Young adult W/BF1 mice had the highest incidence of gastrointestinal
vasculitis (61%), and the highest mean titre of anticardiolipin autoan
tibody. Lesions consisted of sub-intimal fibrinoid degeneration in art
erioles of the duodenum, jejunum and ileum, and were prevented, or alt
ernatively induced by reciprocal marrow transplantations between W/BF1
and B6C3F(1) mice. Mice engrafted with W/BF1 marrow which developed v
asculitis had higher titres of anticardiolipin autoantibodies than eng
rafted mice free of vasculitis (P < 0.005). This represents the first
report of gastrointestinal vasculitis as an aspect of systemic autoimm
unity in lupus-prone mice. The concurrent elevation of anticardiollpin
autoantibody and development of vasculitis suggests that anticardioll
pin autoantibodies, and their proposed thrombogenic and vascular injur
y consequences, contribute to development of microvasculitis in lupus-
prone mice.