Making anti-cytokine therapy more selective: Studies in mice.

Cytokine

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia; Lobachevsky State University of Nizhny Novgorod, Nizhny Novgorod 603950, Russia; Lomonosov Moscow State University, Moscow 199991, Russia; German Rheumatism Research Center (DRFZ), Berlin 10117, Germany. Electronic address:

Published: January 2018

AI Article Synopsis

  • - Cytokines play a crucial role in regulating the immune response, but imbalances in cytokine signaling can trigger autoimmune diseases.
  • - Recent advancements in cytokine inhibitors have improved treatment options for autoimmune diseases, though some patients may experience adverse effects or lack sufficient response.
  • - This review explores new strategies for more selective anti-cytokine therapies and highlights ongoing experimental research using mouse models to support these approaches.

Article Abstract

Cytokines are involved in a wide range of functions shaping the normal immune response, yet inflammatory changes in the immune system due to dysregulated cytokine signaling may lead to the induction of autoimmunity. Cytokine inhibitors have revolutionized the treatment of many autoimmune diseases in recent years. Systemic cytokine ablation, however, is often associated with the development of adverse side effects and some patients simply do not respond to therapy. TNF, IL-1 and IL-6 are the best characterized proinflammatory cytokines considered as the main therapeutic targets for the treatment of several autoimmune and inflammatory diseases. But can anti-cytokine therapy become more selective and thus more efficient? This mini-review discusses several recently emerging paradigms and summarizes current experimental attempts to validate them in mouse studies.

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Source
http://dx.doi.org/10.1016/j.cyto.2016.08.022DOI Listing

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