M. Cumberbatch et al., INTERLEUKIN-1-BETA AND THE STIMULATION OF LANGERHANS CELL-MIGRATION -COMPARISONS WITH TUMOR-NECROSIS-FACTOR-ALPHA, Archives of dermatological research, 289(5), 1997, pp. 277-284
Epidermal Langerhans cells (LC) and the cells into which they mature a
re believed to play a pivotal role in cutaneous immune function, The i
nduction phase of contact sensitization is associated with the migrati
on of LC from the skin and their accumulation as dendritic cells (DC)
in lymph nodes draining the site of exposure, We have demonstrated pre
viously that tumour necrosis factor alpha (TNF-alpha), an epidermal cy
tokine produced by keratinocytes, provides one signal for LC migration
, We describe here experiments designed to evaluate the influence of i
nterleukin 1 beta (IL-1 beta), a product exclusively of LC in murine e
pidermis, on LC migration, LC morphology and DC accumulation, and to c
ompare the effects of this cytokine with those of TNF-alpha. Both cyto
kines induced a significant reduction in the frequency of epidermal LC
and the arrival of DC in draining lymph nodes, Changes in both parame
ters were induced more rapidly following intradermal administration of
TNF-alpha than were observed after treatment with IL-1 beta. However,
the reduction in LC frequency was more persistent with IL-1 beta. Bot
h cytokines caused the activation of LC, characterized by the acquisit
ion of a more dendritic morphology and the increased expression of Ia
molecules, These results demonstrate that IL-1 beta and TNF-alpha can
each stimulate the migration of epidermal LC, but that the changes ind
uced by these cytokines are not identical.