Ad. Mclellan et al., DERMAL DENDRITIC CELLS ASSOCIATED WITH T-LYMPHOCYTES IN NORMAL HUMAN SKIN DISPLAY AN ACTIVATED PHENOTYPE, Journal of investigative dermatology, 111(5), 1998, pp. 841-849
The CMRF-44 and CD83 (HB15) antigens are associated with functional ma
turation and activation of blood dendritic cells (DC). We describe the
expression of these antigens on freshly isolated epidermal Langerhans
cells and dermal DC as well as the distribution of CD83(+)/CMRF-44(+)-activated DC within sections of normal human skin. Fresh Langerhans
cells were prepared by standard techniques and large numbers of enrich
ed (25%-55%), viable dermal DC were obtained using an improved collage
nase treatment protocol with density gradient enrichment, Freshly isol
ated Langerhans cells and dermal DC had similar costimulator and activ
ation antigen expression, and both stimulated moderate levels of allog
eneic T lymphocyte proliferation as determined in the 7 d mixed leukoc
yte reaction. In situ labeling of DC within skin sections revealed a p
opulation of CD83 and CMRF-44 positive dermal cells of which most (app
roximate to 75%) were in intimate contact with CD3(+) T lymphocytes, e
specially in the adnexal regions. In contrast, only 25%-30% of the mor
e numerous CD1a(++) dermal DC population were directly apposed to T ly
mphocytes. The CMRF-44(++) dermal DC population stimulated an allogene
ic mixed leukocyte reaction, confirming their identity as DC. These da
ta, plus comparative data obtained for migratory dermal DC, suggest th
at only a small proportion of dermal DC have been triggered to a more
advanced state of differentiation or activation. The striking associat
ion of the activated dermal DC population with T lymphocytes suggests
that communication between these two cell types in situ may occur earl
y in the immune response to cutaneous antigen.