TY - JOUR
T1 - Myositis Autoantigen Expression Correlates With Muscle Regeneration but Not Autoantibody Specificity
AU - Pinal-Fernandez, Iago
AU - Amici, David R.
AU - Parks, Cassie A.
AU - Derfoul, Assia
AU - Casal-Dominguez, Maria
AU - Pak, Katherine
AU - Yeker, Richard
AU - Plotz, Paul
AU - Milisenda, Jose C.
AU - Grau-Junyent, Josep M.
AU - Selva-O'Callaghan, Albert
AU - Paik, Julie J.
AU - Albayda, Jemima
AU - Corse, Andrea M.
AU - Lloyd, Thomas E.
AU - Christopher-Stine, Lisa
AU - Mammen, Andrew L.
N1 - Funding Information:
We would like to thank Dr. Gustavo Gutierrez-Cruz, Dr. Stefania Dell'Orso, and Faiza Naz (National Institute of Arthritis and Musculoskeletal and Skin Diseases Sequencing Facility) for all technical collaboration in RNA-seq library construction and sequencing. We would like to thank the University of Kentucky Center for Muscle Biology for providing control human muscle samples.
Publisher Copyright:
© 2019 American College of Rheumatology. This article has been contributed to by US Government employees and their work is in the public domain in the USA.
PY - 2019/8
Y1 - 2019/8
N2 - Objective: Although more than a dozen myositis-specific autoantibodies (MSAs) have been identified, most patients with myositis are positive for a single MSA. The specific overexpression of a given myositis autoantigen in myositis muscle has been proposed as initiating and/or propagating autoimmunity against that particular autoantigen. The present study was undertaken to test this hypothesis. Methods: In order to quantify autoantigen RNA expression, RNA sequencing was performed on muscle biopsy samples from control subjects, MSA-positive patients with myositis, regenerating mouse muscles, and cultured human muscle cells. Results: Muscle biopsy samples were available from 20 control subjects and 106 patients with autoantibodies recognizing hydroxymethylglutaryl-coenzyme A reductase (n = 40), signal recognition particles (n = 9), Jo-1 (n = 18), nuclear matrix protein 2 (n = 12), Mi-2 (n = 11), transcription intermediary factor 1γ (n = 11), or melanoma differentiation–associated protein 5 (n = 5). The increased expression of a given autoantigen in myositis muscle was not associated with autoantibodies recognizing that autoantigen (all q > 0.05). In biopsy specimens from both myositis muscle and regenerating mouse muscles, autoantigen expression correlated directly with the expression of muscle regeneration markers and correlated inversely with the expression of genes encoding mature muscle proteins. Myositis autoantigens were also expressed at high levels in cultured human muscle cells. Conclusion: Most myositis autoantigens are highly expressed during muscle regeneration, which may relate to the propagation of autoimmunity. However, factors other than overexpression of specific autoantigens are likely to govern the development of unique autoantibodies in individual patients with myositis.
AB - Objective: Although more than a dozen myositis-specific autoantibodies (MSAs) have been identified, most patients with myositis are positive for a single MSA. The specific overexpression of a given myositis autoantigen in myositis muscle has been proposed as initiating and/or propagating autoimmunity against that particular autoantigen. The present study was undertaken to test this hypothesis. Methods: In order to quantify autoantigen RNA expression, RNA sequencing was performed on muscle biopsy samples from control subjects, MSA-positive patients with myositis, regenerating mouse muscles, and cultured human muscle cells. Results: Muscle biopsy samples were available from 20 control subjects and 106 patients with autoantibodies recognizing hydroxymethylglutaryl-coenzyme A reductase (n = 40), signal recognition particles (n = 9), Jo-1 (n = 18), nuclear matrix protein 2 (n = 12), Mi-2 (n = 11), transcription intermediary factor 1γ (n = 11), or melanoma differentiation–associated protein 5 (n = 5). The increased expression of a given autoantigen in myositis muscle was not associated with autoantibodies recognizing that autoantigen (all q > 0.05). In biopsy specimens from both myositis muscle and regenerating mouse muscles, autoantigen expression correlated directly with the expression of muscle regeneration markers and correlated inversely with the expression of genes encoding mature muscle proteins. Myositis autoantigens were also expressed at high levels in cultured human muscle cells. Conclusion: Most myositis autoantigens are highly expressed during muscle regeneration, which may relate to the propagation of autoimmunity. However, factors other than overexpression of specific autoantigens are likely to govern the development of unique autoantibodies in individual patients with myositis.
UR - http://www.scopus.com/inward/record.url?scp=85067882395&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85067882395&partnerID=8YFLogxK
U2 - 10.1002/art.40883
DO - 10.1002/art.40883
M3 - Article
C2 - 30861336
AN - SCOPUS:85067882395
SN - 2326-5191
VL - 71
SP - 1371
EP - 1376
JO - Arthritis and Rheumatology
JF - Arthritis and Rheumatology
IS - 8
ER -