Necrosis in anti-SRP+ and anti-HMGCR+myopathies
Role of autoantibodies and complement
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Abstract
Objective To characterize muscle fiber necrosis in immune-mediated necrotizing myopathies (IMNM) with anti–signal recognition particle (SRP) or anti–3-hydroxy-3-methylglutarylcoenzyme A reductase (HMGCR) antibodies and to explore its underlying molecular immune mechanisms.
Methods Muscle biopsies from patients with IMNM were analyzed and compared to biopsies from control patients with myositis. In addition to immunostaining and reverse transcription PCR on muscle samples, in vitro immunostaining on primary muscle cells was performed.
Results Creatine kinase levels and muscle regeneration correlated with the proportion of necrotic fibers (r = 0.6, p < 0.001). CD68+iNOS+ macrophages and a Th-1 immune environment were chiefly involved in ongoing myophagocytosis of necrotic fibers. T-cell densities correlated with necrosis but no signs of cytotoxicity were detected. Activation of the classical pathway of the complement cascade, accompanied by deposition of sarcolemmal immunoglobulins, featured involvement of humoral immunity. Presence of SRP and HMGCR proteins on altered myofibers was reproduced on myotubes exposed to purified patient-derived autoantibodies. Finally, a correlation between sarcolemmal complement deposits and fiber necrosis was observed (r = 0.4 and p = 0.004). Based on these observations, we propose to update the pathologic criteria of IMNM.
Conclusion These data further corroborate the pathogenic role of anti-SRP and anti-HMGCR autoantibodies in IMNM, highlighting humoral mechanisms as key players in immunity and myofiber necrosis.
Glossary
- aAb=
- autoantibody;
- CK=
- creatine kinase;
- DM=
- dermatomyositis;
- ENMC=
- European Neuromuscular Center;
- HMGCR=
- 3-hydroxy-3-methylglutarylcoenzyme A reductase;
- IFN=
- interferon;
- IgG=
- immunoglobulin G;
- IL=
- interleukin;
- IMNM=
- immune-mediated necrotizing myopathies;
- MHC=
- major histocompatibility complex;
- MyHC=
- myosin heavy chain;
- NCAM=
- neural cell adhesion molecule;
- SRP=
- signal recognition particle
Footnotes
Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.
↵* These authors contributed equally to this work as co–first authors.
↵† These authors contributed equally to this work as co–last authors.
- Received March 15, 2017.
- Accepted in final form October 27, 2017.
- © 2018 American Academy of Neurology
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