R. Akasu et al., LYMPHOCYTE AND MACROPHAGE SUBSETS IN ACTIVE AND INACTIVE LESIONS OF LICHEN-PLANUS, The American journal of dermatopathology, 15(3), 1993, pp. 217-223
Lichen planus (LP) is a mucocutaneous disease for which the etiology a
nd pathogenesis are poorly understood. We performed an immunohistochem
ical study on formalin-fixed tissue sections of 10 cases of LP using s
ubsets of antibodies to lymphocytes (LCA, CD3, OPD4-CD4, L26, LN1 and
Leu-7), and monocyte-macrophages [lysozyme, KP1-Mac, Factor XIIIa (FXI
IIa) and S-100 protein]. Six cases showed typical histological feature
s of active LP, two cases showed features of active and inactive LP, a
nd two cases showed only inactive LP. In active LP, scattered T cells
(CD3+ and pan T cells) were present in the epidermis, whereas large nu
mbers of CD3+ T cells were present at the dermoepidermal junction and
in the dermis. Approximately 40% of the T cells at the dermoepidermal
junction were of the helper/inducer subset, whereas approximately 80%
of those in the dermis were CD4 positive (helper/inducer T cells). Occ
asional B cells were present in the dermis only. Increased numbers of
S-100-positive Langerhans cells, macrophages expressing lysozyme, and
FXIIIa dendritic cells were present in the epidermis and dermis. The i
nactive lesions showed the presence of a few epidermal Langerhans cell
s and a mild infiltrate of T cells (helper/inducer subset). These resu
lts suggest that in addition to different subsets of T cells and macro
phages, including Langerhans cells, dermal dendritic cells expressing
Factor XIIIa and lysozyme-positive histiocytes play an important role
in lichen planus. They may participate in the destruction and subseque
nt regeneration of the basal layer of the epidermis, or alternatively
may be activated as a result of destruction of the basement membrane i
n LP.