Objective
To investigate p53,bcl-2 and c-myc expression in muscle biopsies from child
ren affected with juvenile dermatomyositis (JDM) and to verify a possible d
ysregulation of programmed cell death in this autoimmune disease.
Methods
Ten muscle biopsies of children affected with JDM were formalin fixed and p
araffin embedded. After haematoxylin and eosin staining, immunohistochemist
ry was performed employing monoclonal antibodies anti-p53, anti-bcl-2 and a
nti-myc. Two normal muscle biopsies were studied as controls.
Results
In the biopsies of JDM, two different patterns of myofibers damage were obs
erved: the first, with tones characterised by necrosis; and the second with
zones where an apoptotic process was dominant. Immunoreactivity for bcl-2
was positive in 8 out of 10 biopsies. P53 and c-myc expression were not pre
sent ira any case. No relationship between the degree of bcl-2 immunostaini
ng and the disease course or outcome was observed.
Conclusions
The over-expression of bcl-2 protein in JDM may suggest a dysregulation of
apoptosis in myofibers. Further studies are required in order to better und
erstand the role of our data in the pathogenetic pathways of the disease.