We have recently shown the expression of lymphoid early developmental marke
rs, including CD104, Thy I, CD1a, Pgp-1 and TdT; by the cells constituting
atopic dermatitis skin infiltrates. To further characterize the cellular ph
enotypes we used an indirect immunoperoxidase assay to analyze sections fro
m two atopic dermatitis lesion skin biopsies using the following as first s
tep monoclonal antibodies (MAB): anti-CD34, CD2, CD5 and CD7. CD34+ mononuc
lear cells and endothelial cells were identified. A strong immunoreaction w
as observed for the T-lineage marker CD2 and CD5, but a poor reaction, if a
ny, was seen for the CD7. Since CD34+ marrow and blood cells are currently
believed to be the major source of the hemopoietic precursors, our data pro
vide further substantial evidence supporting the hypothesis that the atopic
dermatitis skin cell infiltrate represents an ongoing T-lineage in situ di
fferentiation process regulated by the skin epithelial microenvironment The
observed defective expression of the CD7 antigen requires further investig
ation for its confirmation as a possible constant feature in atopic dermati
tis.