Biomarkers are decision-making tools at the basis of clinical diagnostics and essential for guiding therapeutic treatments. In this context, autoimmune diseases represent a class of disorders that need early diagnosis and steady monitoring. In these diseases, the immune system recognizes some antigens no more as self and it is now accepted that post-translational modifications may affect the immunogenicity of self-protein antigens, triggering an autoimmune response. Therefore, osttranslationally modified peptides are the best candidate to develop synthetic probes detecting autoantibodies as disease biomarkers. A “Chemical Reverse Approach” to select synthetic peptides bearing specific post-translational modifications able to fishing out autoantibodies from patients’ biological fluids, can be successfully applied for the development of specific noninvasive diagnostic/prognostic assays of autoimmune diseases.

Peptides as autoimmune diseases antigenic probes. A peptide-based reverse approach to detect biomarkers of autoimmune diseases

Chelli M;
2007

Abstract

Biomarkers are decision-making tools at the basis of clinical diagnostics and essential for guiding therapeutic treatments. In this context, autoimmune diseases represent a class of disorders that need early diagnosis and steady monitoring. In these diseases, the immune system recognizes some antigens no more as self and it is now accepted that post-translational modifications may affect the immunogenicity of self-protein antigens, triggering an autoimmune response. Therefore, osttranslationally modified peptides are the best candidate to develop synthetic probes detecting autoantibodies as disease biomarkers. A “Chemical Reverse Approach” to select synthetic peptides bearing specific post-translational modifications able to fishing out autoantibodies from patients’ biological fluids, can be successfully applied for the development of specific noninvasive diagnostic/prognostic assays of autoimmune diseases.
2007
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/453164
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