Cf. Wahlgren et al., ITCH AND INFLAMMATION-INDUCED BY INTRADERMALLY INJECTED INTERLEUKIN-2IN ATOPIC-DERMATITIS PATIENTS AND HEALTHY-SUBJECTS, Archives of dermatological research, 287(6), 1995, pp. 572-580
To explore the pruritogenic and inflammatory effects of cytokines, a s
ingle dose of 20 mu g recombinant human interleukin-2 was injected int
radermally into eight patients with atopic dermatitis and eight health
y controls, The study was double-blind and randomized with glucose as
a negative control, The effects were evaluated by recording local itch
and erythema over 72 h and by examining skin biopsies taken at 24 h a
nd 72 h. In patients and controls, interleukin-2 provoked a low-intens
ity local itch with maximal intensity between 6 h and 48 h and erythem
a with maximal extension between 12 h and 72 h. In the atopic dermatit
is patients, these reactions tended to appear earlier and were less pr
onounced than in the healthy controls, Interleukin-2 induced dermal mo
nonuclear cell infiltrates consisting mainly of CD3(+) cells. A majori
ty of the T cells were CD4(+). The number of dermal CD25(+), HLA-DR(+)
and ICAM-1(+) cells was also increased at the interleukin-2 injection
sites, In the epidermis, interleukin-2 induced spongiosis and exocyto
sis as well as HLA-DR(+) and ICAM-1(+) keratinocytes, The microscopic
findings tended to be more prominent at 72 h than at 24 h in both grou
ps, but with a somewhat slower onset in the atopic dermatitis patients
, In conclusion, a single intradermal injection of interleukin-2 induc
ed local itch, erythema, dermal T-cell infiltrates, spongiosis, exocyt
osis and activation of keratinocytes both in atopic dermatits patients
and in healthy controls.