M. Uehira et al., IMMUNOLOGICAL ABNORMALITIES EXHIBITED IN IL-7 TRANSGENIC MICE WITH DERMATITIS, Journal of investigative dermatology, 110(5), 1998, pp. 740-745
Interleukin (IL)-7 transgenic mice, which we established previously, d
eveloped severe dermatitis characterized by massive infiltration of ga
mma delta T cells in the dermal lesion. To fully understand the pathol
ogy of this intriguing skin disease, we examined several immunologic f
eatures of dermis infiltrating lymphocytes from the lesional skin of I
L-7 transgenic mice. We observed a moderate response to mitogens, a po
or response to alloantigens, and the absence of cytotoxic activities t
o several tumor cell lines and skin derived cells regardless of the pr
esence of IL-2 or IL-7., On the other hand, dermis infiltrating lympho
cytes could proliferate with exogenous IL-2 and IL-7., Moreover, rever
se transcriptase polymerase chain reaction and fluorescence activated
cell sorter analysis revealed that dermis infiltrating lymphocytes exp
ressed various cytokines including IL-4 and IL-7, and several activati
on markers for T cells (CD44, CD69, IL-2R alpha), in addition to IL-7R
alpha., In the sera of the affected mice, hyper epsilon-globulinemia
was observed. These findings suggested that dermis infiltrating lympho
cytes proliferated in an activated state in the skin lesion in an auto
crine and/or paracrine manner and produced Th2 type cytokines that mig
ht evoke immunologic abnormalities, This study and previous findings s
uggest that IL-7 transgenic mouse with dermatitis offer the potential
of serving as a useful tool for investigating the immunologic role of
cutaneous gamma delta T cells, especially their participation in IgE p
roduction in vivo.