V. Kodelja et al., LANGERHANS CELLS DO NOT EXPRESS ALTERNATIVE MACROPHAGE ACTIVATION-ASSOCIATED CC-CHEMOKINE (AMAC)-1, Research in immunology (Paris), 149(7-8), 1998, pp. 633-637
We have cloned a novel human CC chemokine, alternative macrophage acti
vation-associated CC chemokine (AMAC)-1 that is highly homologous to m
acrophage inflammatory protein (MIP)-1 alpha. In contrast to MIP-1 alp
ha AMAC-1 is induced in macrophages by Th2-associated cytokines IL4, I
L13, and IL10 in vitro; in addition, AMAC-1 is expressed by Th1-suppre
ssive alveolar macrophages in vivo. Surprisingly, however, AMAC-1 is a
lso expressed by GM-CSF-induced, in vitro monocyte-derived dendritic c
ells when treated by IL4. Here, we present a detailed analysis of AMAC
-1 expression in monocyte-derived dendritic cells in vitro and show th
at the prime dendritic cells in vivo, i.e. epidermal Langerhans cells,
do not express AMAC-1 mRNA. In conclusion, AMAC-1 is a novel CC chemo
kine whose Th2-associated expression pattern in alternatively activate
d suppressor macrophages in vivo and in vitro and its absence from epi
dermal Langerhans cells in vivo suggest that it may be involved in inh
ibition of Th1 reactions and in tolerance induction.