M. Olsson et al., ACCUMULATION OF T-LYMPHOCYTES AND EXPRESSION OF INTERLEUKIN-2 RECEPTORS IN NONRHEUMATIC STENOTIC AORTIC VALVES, Journal of the American College of Cardiology, 23(5), 1994, pp. 1162-1170
Objectives. Cell specific antibodies were used to identify immunocompe
tent cells in a comparison of valves from patients who had symptomatic
tricuspid aortic stenosis with subjects who had no evidence of valvul
ar heart disease. Background. Nonrheumatic valvular aortic stenosis is
the most common valvular heart disease among adults. The biologic pro
cesses involved in the development of this disease are poorly understo
od. Methods. Tricuspid stenotic aortic valves were obtained from 19 pa
tients undergoing surgery for nonrheumatic valvular aortic stenosis, a
nd 10 control valves were collected at autopsy. The valves were fixed
in formaldehyde, cryosectioned and stained with antibodies against fib
roblasts, endothelial cells, macrophages, T lymphocytes and interleuki
n-2 receptors. A subset of valves were also analyzed with antibodies a
gainst T-helper cells and cytotoxic T cells. Results. Stenotic valves
were characterized by a basal accumulation of calcium deposits and a c
ell-rich subendothelial thickening. The immunohistologic analysis indi
cated that the cells in the subendothelial connective tissue were fibr
oblasts. T lymphocytes appeared to be the most common cell type in the
vicinity of the calcium deposits and were also found close to the end
othelial lining of the valves. T helper cells were more frequent than
cytotoxic T cells. Expression of interleukin-2 receptors occurred at t
he same location as T lymphocytes. Control valves lacked subendothelia
l thickening and contained only few cells reacting with antibodies aga
inst lymphocytes and macrophages. Conclusions. The presence of activat
ed T lymphocytes in tricuspid stenotic valves suggests that immunologi
c mechanisms may be involved in the etiology of nonrheumatic aortic st
enosis.