Sr. Stevens et al., LONG-TERM EFFECTIVENESS AND SAFETY OF RECOMBINANT HUMAN INTERFERON-GAMMA THERAPY FOR ATOPIC-DERMATITIS DESPITE UNCHANGED SERUM IGE LEVELS, Archives of dermatology, 134(7), 1998, pp. 799-804
Objective: To assess the long-term effects of recombinant human interf
eron gamma treatment of atopic dermatitis (AD). Design: Case series. P
atients were treated for up to 24 months. Setting: University dermatol
ogy outpatient clinics in Ann Arbor, Mich, and Portland, Ore. Patients
: Twenty-four of 32 eligible patients who participated in a previously
reported, 12-week, double-blind, placebo-controlled study of recombin
ant human interferon gamma treatment for AD were enrolled. Interventio
n: Patients self-administered recombinant human interferon gamma, 50 m
u g/m(2), by daily subcutaneous injection. Main Outcome Measures: Over
all response; body surface area of involvement; clinical severity scor
es for pruritus, erythema, edema, excoriations, dryness, scaling, and
lichenification; other atopic symptoms; and laboratory parameters, inc
luding serum IgE levels, were monitored at quarterly visits. Results a
t 1 and 2 years were compared with baseline values. Results: All effic
acy parameters improved (P<.05). For example, pruritus was reduced by
50% after both 1 (n = 24, P<.001) and 2 (n = 16, P =.005) years. Aller
gic conjunctivitis and allergic rhinitis also improved (P<.01). Eosino
phil counts decreased significantly (P<.001). IgE levels increased. Cl
inical improvement more closely correlated with changes in eosinophil
counts (r=0.3-0.5) than.with changes in IgE levels (r=0.0-0.2). Only 1
patient discontinued therapy because of adverse effects (flulike symp
toms). Conclusions: The initial efficacy and adverse effects reported
For recombinant human interferon gamma treatment of patients with AD w
ere maintained after 2 years of long-term use. Recombinant human inter
feron gamma seems to be a well-tolerated and effective agent in the lo
ngterm therapy of patients with AD. Therapies that correct cellular im
mune defects, but not humoral immune defects, may be effective in the
treatment of patients with AD.