Influence of Immunogenicity on the Long-Term Efficacy of Infliximab in Crohn's Disease
Filip Baert, M.D., Maja Noman, M.D., Severine Vermeire, M.D., Ph.D., Gert Van Assche, M.D., Ph.D., Geert D' Haens, M.D., Ph.D., An Carbonez, Ph.D., and Paul Rutgeerts, M.D., Ph.D.
Background Treatment with infliximab, a chimeric monoclonalIgG1 antibody against tumor necrosis factor, can result in theformation of antibodies against infliximab. We evaluated theclinical significance of these antibodies in patients with Crohn'sdisease.
Methods In a cohort of 125 consecutive patients with Crohn'sdisease who were treated with infliximab infusions, we evaluatedthe concentrations of infliximab and of antibodies against infliximab,clinical data, side effects (including infusion reactions),and the use of concomitant medications before and 4, 8, and12 weeks after each infusion.
Results A mean of 3.9 infusions (range, 1 to 17) per patientwere administered over a mean period of 10 months. Antibodiesagainst infliximab were detected in 61 percent of patients.The presence of concentrations of 8.0 µg per milliliteror greater before an infusion predicted a shorter duration ofresponse (35 days, as compared with 71 days among patients withconcentrations of less than 8.0 µg per milliliter; P<0.001)and a higher risk of infusion reactions (relative risk, 2.40;95 percent confidence interval, 1.65 to 3.66; P<0.001). Infliximabconcentrations were significantly lower at four weeks amongpatients who had had an infusion reaction than among patientswho had never had an infusion reaction (median, 1.2 vs. 14.1µg per milliliter; P<0.001). Patients who had infusionreactions had a median duration of clinical response of 38.5days, as compared with 65 days among patients who did not havean infusion reaction (P<0.001). Concomitant immunosuppressivetherapy was predictive of low titers of antibodies against infliximab(P<0.001) and high concentrations of infliximab four weeksafter an infusion (P<0.001).
Conclusions The development of antibodies against infliximabis associated with an increased risk of infusion reactions anda reduced duration of response to treatment. Concomitant immunosuppressivetherapy reduces the magnitude of the immunogenic response.
Source Information
From the Department of Internal Medicine, Division of Gastroenterology, University Hospital Gasthuisberg (F.B., M.N., S.V., G.V.A., G.D., P.R.); and the University Center for Statistics, Leuven University (A.C.) both in Leuven, Belgium.
Address reprint requests to Dr. Rutgeerts at the Department of Internal Medicine, UZ Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium, or at paul.rutgeerts{at}uz.kuleuven.ac.be.
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