C. Gasche et al., PROSPECTIVE EVALUATION OF INTERFERON-ALPHA IN TREATMENT OF CHRONIC ACTIVE CROHNS-DISEASE, Digestive diseases and sciences, 40(4), 1995, pp. 800-804
Several case reports suggested good effects of interferon-cu in patien
ts with Crohn's disease. In addition, a decreased production of interf
eron-alpha in Crohn's disease has been shown in vitro. Treatment with
interferon-alpha may activate intestinal natural killer cells and down
regulate the overproduction of inflammatory cytokines like interleukin
-6 in Crohn's disease. To evaluate the clinical efficacy of interferon
-alpha, we treated 12 patients with a chronic active course of Crohn's
disease with recombinant human interferon-alpha prospectively for 24
weeks. Prednisolone was continuously tapered and discontinued at week
12. The end point of the study was the prevention of worsening of clin
ical symptoms defined with the Crohn's disease activity index and was
monitored by acute-phase proteins, interleukin-6 serum concentrations,
and endoscopy. The biochemical activity of interferon-alpha was measu
red by 2',5'-oligo adenylate serum levels. The end point of the study
was reached in four patients (33%). In these patients the final Crohn'
s disease activity index was above 150, which means that they did not
achieve clinical remission. All other patients (66%) did not respond t
o interferon-alpha and had to be withdrawn prematurely. Interferon-alp
ha did not show any beneficial effect on interleukin-6 or acute-phase
protein concentrations and on endoscopic activity. The 2',5'-oligo ade
nylate levels continuously increased during interferon therapy. Consid
erable side effects were noted. These results fail to demonstrate a th
erapeutic role of interferon-alpha in chronic active Crohn's disease.