Evaluation of the impact of neutralizing antibodies on IFNβ response

IFN beta therapeutic action depends on a sequence of biological steps: i) the interaction between interferon beta (IFN beta) and its receptor (IFNAR) located at the cell surface of peripheral blood mononuclear cells; ii) activation of second messengers; iii) transcription of several genes containing specific ISRE regions (Interferon Stimulated Response Elements); and iv) synthesis of specific proteins. Although IFN beta therapy has improved treatment options of patients with multiple sclerosis (MS), the long-term efficacy of IFN beta s can be compromised due to the development of neutralizing antibodies (NAbs). High titer NAbs develop in about 15% of patients; they abolish IFN beta biological activity and consequently the therapeutic action of IFN beta. Different IFN beta preparations carry different risks of developing NAbs, ranging from 3 to 28%. The risk of inducing NAbs must be considered in the selection of treatment. Guidelines for NAbs testing and the therapeutic decision in case of NAbs positivity have been established. NAbs positivity predicts MRI and clinical activity. Precocious identification of Nabs-positive patients and switch to alternative treatments can improve the percentage of responders and allow a better allocation of relevant economical resources. (C) 2015 Elsevier B.V. All rights reserved.