W. Dummer et al., EXPRESSION OF CD30 ON T-HELPER CELLS IN THE INFLAMMATORY INFILTRATE OF ACUTE ATOPIC-DERMATITIS BUT NOT OF ALLERGIC CONTACT-DERMATITIS, Archives of dermatological research (Print), 290(11), 1998, pp. 598-602
The CD30 molecule has been proposed as a marker for a subset of CD4(+)
CD35RO(+) (memory) T cells with potent B cell helper activity producin
g IL-5 and IFN-gamma and as a specific marker for Th2 cells. Recently,
an association has been demonstrated between elevated serum levels of
soluble CD30, which is shed by CD30(+) cells in vitro and in vivo, an
d atopic dermatitis but not respiratory atopic disorders or allergic c
ontact dermatitis. We studied the expression of CD30 in the inflammato
ry infiltrate of atopic dermatitis compared with that of allergic cont
act dermatitis, with special regard to skin disease activity (acute vs
subacute/chronic). Biopsies were obtained from 16 patients suffering
from atopic dermatitis (acute n = 6, subacute/chronic n = 10), from 7
patients with acute allergic contact dermatitis and from 5 positive pa
tch-test reactions. Paraffin-embedded as well as snap-frozen material
was stained with anti-CD30 and anti-CD45RO mAbs according to standard
procedures. Double-staining procedures for CD30CD3, CD30CD4, CD30CD45R
O and CD30CD68 were also performed. Abundant CD45RO(+) cells were dete
cted both in atopic dermatitis and in allergic contact dermatitis lesi
ons. We found scattered CD30(+) cells in only one of six formalin-fixe
d paraffin-embedded acute atopic dermatitis biopsies, but in all of th
e respective snap-frozen specimens, possibly because CD30 expression o
n atopic dermatitis infiltrating cells is weak and sensitive to formal
in fixation and paraffin embedding. CD30CD3 and CD30CD4 double stainin
g identified CD30(+) cells to be helper T lymphocytes. No significant
CD30 expression (either in paraffin-embedded or in frozen material) co
uld be found in subacute/chronic atopic dermatitis lesions or in any o
f the specimens of allergic contact dermatitis. The results suggest a
specific regulatory function of CD30(+) T cells in acute atopic dermat
itis. With respect to the view that CD30 is a marker for Th2 cells, ou
r observations confirm previous findings that Th2 cells predominate in
the infiltrate particularly of acute atopic dermatitis. CD30 expressi
on in acute atopic dermatitis but not in acute allergic contact dermat
itis might be helpful in the histological differentiation of these dis
orders and in the further characterization of atopy patch testing.