Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies

Idiopathic inflammatory myopathies represent still a diagnostic and therapeutic challenge in different disciplines including neurology, rheumatology, and dermatology. In recent years, the spectrum of idiopathic inflammatory myopathies has been significantly extended and the different manifestations...

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Main Authors: Bruno Stuhlmüller, Udo Schneider, José-B. González-González, Eugen Feist
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-05-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fneur.2019.00438/full
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author Bruno Stuhlmüller
Udo Schneider
José-B. González-González
José-B. González-González
Eugen Feist
author_facet Bruno Stuhlmüller
Udo Schneider
José-B. González-González
José-B. González-González
Eugen Feist
author_sort Bruno Stuhlmüller
collection DOAJ
description Idiopathic inflammatory myopathies represent still a diagnostic and therapeutic challenge in different disciplines including neurology, rheumatology, and dermatology. In recent years, the spectrum of idiopathic inflammatory myopathies has been significantly extended and the different manifestations were described in more detail leading to new classification criteria. A major breakthrough has also occurred with respect to new biomarkers especially with the characterization of new autoantibody-antigen systems, which can be separated in myositis specific antibodies and myositis associated antibodies. These markers are detectable in approximately 80% of patients and facilitate not only the diagnostic procedures, but provide also important information on stratification of patients with respect to organ involvement, risk of cancer and overall prognosis of disease. Therefore, it is not only of importance to know the significance of these markers and to be familiar with the optimal diagnostic tests, but also with potential limitations in detection. This article focuses mainly on antibodies which are specific for myositis providing an overview on the targeted antigens, the available detection procedures and clinical association. As major tasks for the near future, the need of an international standardization is discussed for detection methods of autoantibodies in idiopathic inflammatory myopathies. Furthermore, additional investigations are required to improve stratification of patients with idiopathic inflammatory myopathies according to their antibody profile with respect to response to different treatment options.
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spelling doaj.art-e6788e7edd56487c9c0ff53a92e05ca82022-12-21T20:00:13ZengFrontiers Media S.A.Frontiers in Neurology1664-22952019-05-011010.3389/fneur.2019.00438440739Disease Specific Autoantibodies in Idiopathic Inflammatory MyopathiesBruno Stuhlmüller0Udo Schneider1José-B. González-González2José-B. González-González3Eugen Feist4Department of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, GermanyDepartment of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, GermanyDepartment of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, GermanyLabor Berlin-Charité Vivantes GmbH, Berlin, GermanyDepartment of Rheumatology and Clinical Immunology, Charité-Universitätsmedizin, Berlin, GermanyIdiopathic inflammatory myopathies represent still a diagnostic and therapeutic challenge in different disciplines including neurology, rheumatology, and dermatology. In recent years, the spectrum of idiopathic inflammatory myopathies has been significantly extended and the different manifestations were described in more detail leading to new classification criteria. A major breakthrough has also occurred with respect to new biomarkers especially with the characterization of new autoantibody-antigen systems, which can be separated in myositis specific antibodies and myositis associated antibodies. These markers are detectable in approximately 80% of patients and facilitate not only the diagnostic procedures, but provide also important information on stratification of patients with respect to organ involvement, risk of cancer and overall prognosis of disease. Therefore, it is not only of importance to know the significance of these markers and to be familiar with the optimal diagnostic tests, but also with potential limitations in detection. This article focuses mainly on antibodies which are specific for myositis providing an overview on the targeted antigens, the available detection procedures and clinical association. As major tasks for the near future, the need of an international standardization is discussed for detection methods of autoantibodies in idiopathic inflammatory myopathies. Furthermore, additional investigations are required to improve stratification of patients with idiopathic inflammatory myopathies according to their antibody profile with respect to response to different treatment options.https://www.frontiersin.org/article/10.3389/fneur.2019.00438/fullmyositisinflammationautoantibodiesantigensbiomarker
spellingShingle Bruno Stuhlmüller
Udo Schneider
José-B. González-González
José-B. González-González
Eugen Feist
Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
Frontiers in Neurology
myositis
inflammation
autoantibodies
antigens
biomarker
title Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
title_full Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
title_fullStr Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
title_full_unstemmed Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
title_short Disease Specific Autoantibodies in Idiopathic Inflammatory Myopathies
title_sort disease specific autoantibodies in idiopathic inflammatory myopathies
topic myositis
inflammation
autoantibodies
antigens
biomarker
url https://www.frontiersin.org/article/10.3389/fneur.2019.00438/full
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AT udoschneider diseasespecificautoantibodiesinidiopathicinflammatorymyopathies
AT josebgonzalezgonzalez diseasespecificautoantibodiesinidiopathicinflammatorymyopathies
AT josebgonzalezgonzalez diseasespecificautoantibodiesinidiopathicinflammatorymyopathies
AT eugenfeist diseasespecificautoantibodiesinidiopathicinflammatorymyopathies