N. Djemadjioudjiel et al., IMMUNOHISTOCHEMICAL IDENTIFICATION OF TYPE-II ALTERNATIVELY ACTIVATEDDENDRITIC MACROPHAGES (RM-3 1(+++), MS-1(+/-), 25F9(-)) IN PSORIATIC DERMIS/, Archives of dermatological research, 288(12), 1996, pp. 757-764
Immunological mechanisms play an important role in the pathogenesis of
psoriasis. Lesional psoriatic skin-derived T-cell clones have been sh
own to stimulate keratinocyte proliferation and to predominantly expre
ss a T-helper type 1 cytokine pattern. However, T-helper type 2-like c
ytokines have also been identified in some psoriatic T-cell clones. In
parallel to the T-helper type 1/type 2 dichotomy, a distinction betwe
en interferon-gamma-induced (classically activated) macrophages and in
terleukin-4/glucocorticoid-induced (alternatively activated) macrophag
es has been put forward as a conceptual framework for a better underst
anding of immunopathological processes. In the present study, the phen
otype of mononuclear phagocytes in psoriatic skin lesions (n = 21), al
lergic contact dermatitis (n = 4) and normal skin (n = 2) was investig
ated using a panel of monoclonal antibodies (mAb) against monocytes/ma
crophages and dendritic cells (mAb MS-1, RM 3/1, and 25F9 against subs
ets of in vitro alternatively activated macrophages, and mAb against m
yeloid antigens CD1a, CD11b, CD11c, CD34, CD36, and CD68). With regard
to mononuclear phagocytes, psoriatic skin was found to be compartment
alized into epidermis, subepidermal space, and upper and lower dermis.
RM 3/1(+++), MS-1(+/-), 25F9(-) dendritic macrophages previously clas
sified as type II alternatively activated macrophages were the dominan
t dermal macrophage population in psoriatic skin, while intraepidermal
and epithelium-lining macrophages expressed a different, presumably c
lassically activated, macrophage phenotype (RM 3/1(-), MS-1(-), 25F9(-
), CD68(++), CD11b(++)). In allergic contact dermatitis, a classical T
-helper type 1 disease, RM 3/1(+++) macrophages were less prominent. S
ince MS-1 high molecular weight protein is much more sensitive to inte
rferon-gamma-induced suppression than RM 3/1 antigen, a predominance o
f T-helper type 1 cytokines in psoriasis could explain why dermal dend
ritic macrophages do not express the fully induced MS-1(+++), RM 3/1(++), 25F9(+/-) phenotype of type I alternatively activated macrophages
.