Circulating CLA(+) lymphocytes from children with atopic dermatitis contain an increased percentage of cells bearing staphylococcal-related T-cell receptor variable segments
Mj. Torres et al., Circulating CLA(+) lymphocytes from children with atopic dermatitis contain an increased percentage of cells bearing staphylococcal-related T-cell receptor variable segments, CLIN EXP AL, 28(10), 1998, pp. 1264-1272
Background Atopic dermatitis is an allergic T-cell mediated skin inflammati
on. Staphylococcus aureus colonization is very common in cutaneous atopic d
ermatitis lesions. The cutaneous lymphocyte-associated antigen (CLA) is a T
cell skin homing receptor that defines T lymphocytes associated with the c
utaneous immune response.
Objective To study whether CLA(+) T cells from atopic dermatitis children p
resent a selective expression far Staphylococcus aureus-related TCR V beta
segments.
Methods Peripheral blood T cells were stained with HECA-452 (anti-CLA) and
a panel of TCR V beta specific monoclonal antibodies and analysed by flow c
ytometry.
Results Atopic dermatitis patients have a higher percentage of circulating
CLA(+) CD3(+) lymphocytes compared with healthy controls. Patients with act
ive atopic dermatitis during the study expressed a higher percentage of cel
ls positive for the TCR V beta 2 and V beta 5.1 segments in the CLA(+) but
not in the CLA(-) subset. These TCR V beta s are recognized by staphylococc
al superantigens. Moreover, there was an increased percentage of HLA-DR+ ex
pression by CLA(+) V beta 5.1(+) T cells in patients with active atopic der
matitis, but those patients whose eczema was inactive had very similar valu
es to healthy controls regarding TCR V beta and HLA-DR phenotype in circula
ting CLA(+) T lymphocytes.
Conclusion Our data indicate that circulating skin-homing T cells of patien
ts with active atopic dermatitis contain an increased percentage of cells b
earing TCR V beta segments related with Staphylococcus aureus. Staphylococc
us superantigens may therefore trigger expansion or at least circulation of
appropriate CLA(+) T cells.