PATIENTS WITH ALLERGIC CONTACT-DERMATITIS TO NICKEL AND NONALLERGIC INDIVIDUALS DISPLAY DIFFERENT NICKEL-SPECIFIC T-CELL RESPONSES - EVIDENCE FOR THE PRESENCE OF EFFECTOR CD8(-CELLS() AND REGULATORY CD4(+) T)
A. Cavani et al., PATIENTS WITH ALLERGIC CONTACT-DERMATITIS TO NICKEL AND NONALLERGIC INDIVIDUALS DISPLAY DIFFERENT NICKEL-SPECIFIC T-CELL RESPONSES - EVIDENCE FOR THE PRESENCE OF EFFECTOR CD8(-CELLS() AND REGULATORY CD4(+) T), Journal of investigative dermatology, 111(4), 1998, pp. 621-628
To investigate the mechanisms underlying the expression of allergic co
ntact dermatitis, we compared the characteristics of nickel (Ni)-speci
fic T cell responses in 10 patients with allergic contact dermatitis t
o Ni and in 10 healthy, nonallergic individuals. CD4(+) T cells purifi
ed from peripheral blood of both allergic and nonallergic subjects pro
liferated similarly to NiSO4 in vitro, with the responses mostly restr
icted to CD4(+) CD45RO(+) memory T cells. In contrast, Ni-specific CD8
(+) T cell responses were detected only in allergic patients. Limiting
dilution assay confirmed a high frequency of Ni-specific CD4(+) T cel
ls in both individual categories, and of Ni-specific CD8(+) T cells in
allergic patients, but not in nonallergic persons. Ni-specific CD4(+)
T cell clones prepared from nonallergic subjects displayed lower inte
rferon-gamma and higher interleukin-10 production compared with T cell
clones from allergic patients. The T cell skin-homing receptor, cutan
eous lymphocyte-associated antigen, was expressed on the large majorit
y of specific CD4(+) clones from both the groups. Finally, Ni-specific
CD8(+) clones prepared from patients also expressed the cutaneous lym
phocyte-associated antigen receptor, and released high interferon-gamm
a and no interleukin-4. In aggregate, the results suggest that the pre
sence of specific CD8(+) T cells and a distinct pattern of cytokine re
lease (e.g., an augmented production of interleukin-10) by CD4(+) T ce
lls can be important elements in determining whether a hapten induces
allergy or a silent immune response.