Crohn's disease (CD) is characterized by transmural inflammatory disease in
volving any portion of the gastrointestinal tract. Patients with CD have in
creased mucosal concentrations of the cytokine tumor necrosis factor-alpha
(TNF-alpha), a key mediator of mucosal inflammation. In addition, TNF-alpha
has multiple biologic activities involved in apoptosis, metabolism, and ac
tivation of granulocytes, lymphocytes, eosinophils, fibroblasts, chondrocyt
es, and endothelial cells. Recently, infliximab has emerged as a novel chim
eric monoclonal antibody that inhibits TNF-alpha. Infliximab is indicated f
or the treatment of moderately to severely active CD in patients having an
inadequate response to conventional therapy. To date, a small number of cli
nical trials with infliximab have demonstrated efficacy and tolerability wh
en the agent is initiated as a 5-mg/kg single intravenous infusion. In pati
ents with fistulizing CD, administration of 2 subsequent 5-mg/kg doses 2 an
d 6 weeks after the initial dose appears to be efficacious. Infliximab seem
s to be a promising therapeutic strategy for patients with refractory CD.