Modulatory cytokines such as IL-4 and IL-10 looked promising biologicals, but suffered from poor exposure at the inflamed joints when administered via the patient-friendly subcutaneous route. Immunocytokines have now been engineered with tissue targeting potential and are a possible solution to this problem, although challenges still exist. Local inflammatory processes cause destruction of extracellular matrix (ECM) components, leading to neoeptitopes, and/or elicit the synthesis of new ECM components. This makes ECM elements interesting targets for antibodymediated recognition and retention, to achieve higher levels of immunocytokines at the site of therapeutic interference. The study presented by Schwager and colleagues shows that targeted delivery of IL-10 is more efficacious in experimental arthritis. Clinical studies are warranted to show whether this strategy works for all rheumatoid arthritis patients or is better for subgroups with a defined ECM phenotype. In principle, the scFv-targeting system is plastic enough to allow for personalized strategies.© 2009 BioMed Central Ltd.
CITATION STYLE
Van de Loo, F. A., & Van den Berg, W. B. (2009, November 6). Immunocytokines: The long awaited therapeutic magic bullet in rheumatoid arthritis? Arthritis Research and Therapy. https://doi.org/10.1186/ar2835
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