The MRL-Fas(lpr) mouse, a model of multisystemic, organ non-specific autoim
mune disease, has been proposed as a model of immune-mediated inner ear dis
ease. Preliminary studies indicate that it develops cochlear pathology focu
sed in the stria vascularis including intracellular edema and degeneration
which develops in the absence of an inflammatory infiltrate but in the pres
ence of antibody deposition. It was thus hypothesized that the antibodies f
ound in the stria were mediating a direct pathologic effect on this structu
re, without recruiting classical inflammatory mediators. It was further hyp
othesized that the antibodies deposited within the stria would be derived f
rom the non-complement fixing isotypes and subclasses, which are known to b
e able to mediate direct pathologic effects on target tissues. This study u
tilized immunohistologic techniques to identify the antibody isotypes and s
ubclasses deposited within the stria vascularis of the MRL-Fas(lpr) mouse.
Results indicate that all antibody isotypes and subclasses can be identifie
d within the stria vascularis in the absence of complement. Thus, antibody
deposition was not restricted to non-complement fixing antibodies. While it
is possible that antibodies are mediating direct pathologic effects within
the stria, the non-specific nature of the antibody deposition may indicate
that these antibodies are not responsible for the observed pathology. Rath
er, other mechanisms, such as metabolic and genetic etiologies, must also b
e considered. (C) 1999 Published by Elsevier Science B.V. All rights reserv
ed.