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Idiopathic inflammatory myopathies (IIMs) are rare, heterogeneous, autoimmune musculoskeletal diseases, characterised clinically by muscle weakness. Extramuscular involvement includes the skin, respiratory and cardiovascular systems. Genetic and environmental factors contribute to IIM susceptibility, and viral or bacterial infection may contribute to disease pathogenesis.
Both the innate and adaptive immune systems are important in IIM pathology. Two-thirds of affected individuals have known myositis-specific or associated autoantibodies, often linked to particular clinical features,1 and directed against proteins involved in key intracellular processes. Interferon pathways are differentially activated in clinical subtypes of myositis2; this interferon response is critical to protect the host against viral infection and modulate the antiviral immune response.
We recently used a high-throughput approach combining disease-specific immunoglobulin epitope signature enrichment and antigen identification from the total microbial ‘exposome’ (including viruses, bacteria, archaea and fungi) and human proteins.3 We applied this serum antibody repertoire analysis pipeline to investigate the microbial and autoantigen antibody repertoire accumulated throughout life in 20 adult-onset dermatomyositis patients seropositive for TIF1γ (TRIM33) autoantibodies, compared with 20 age-matched and gender-matched healthy controls.3
Human coronaviruses are associated with the common cold, but can lead to fatal inflammatory responses and acute lung injury. Emergence of a novel coronavirus has caused a recent global pandemic of severe acute respiratory syndrome (SARS) in humans (COVID-19).4 Whole genome phylogenetic analyses suggest that the COVID-19 coronavirus SARS-CoV-2 shares high sequence similarity with bat coronaviruses and the host reservoir is bats.4
Due to the current coronavirus pandemic, here, we focused our analysis on epitopes mapping to the coronaviridae family. In dermatomyositis patients3, we identified enrichment of immunogenic linear epitopes (minimum 10 consecutive amino acids) mapping to 20 coronaviridae species, including 10 discrete epitopes mapping to three bat-coronavirus species. To investigate whether these 10 bat-coronavirus epitopes share sequence identity with human SARS-CoV-2, we carried out local alignment of the identified epitope sequences and the orf1ab polyprotein of SARS-CoV-2 (NCBI RefSeq: YP_009724389.1), and identified six distinct epitopes with high sequence identity (table 1). The epitopes were further queried against the database of non-redundant protein sequences (NCBI Blastp suite). Three linear epitopes of six amino acid length were highly specific for SARS-CoV-2 (table 1, figure 1). These epitopes map to SARS-CoV-2 2'-O-ribose methyltransferase, RNA-dependent RNA polymerase and 3'-to-5' exonuclease proteins. All three epitopes show extremely high conservation among currently available SARS-CoV-2 polyprotein sequences from the NCBI database (NCBI Multiple Alignment).
We subsequently investigated whether these epitopes have been experimentally identified as B cell and T cell immunogenic epitopes from studies of epidemic-causing virus SARS-CoV, or computationally predicted from SARS-CoV-2. Epitope ‘DDAVVC’ in the RNA-dependent RNA polymerase protein is a highly ranked CD8 T cell predicted epitope identified from the Immune Epitope Database and Analysis Resource, showing HLA-A*01:01 restriction.5
The coronavirus genome encodes four structural proteins; spike, nucleocapsid, membrane and envelope proteins. SARS-CoV-2 spike glycoproteins promote cell entry through attachment to the host ACE 2 receptor, and subsequent fusion between viral and host cell membranes to facilitate viral entry,6 and are the main target of antibodies. Here, we report identification of three immunogenic linear epitopes with high sequence identity to SARS-CoV-2 proteins in patients with autoimmune dermatomyositis, including ‘DDAVVC’ in the RNA-dependent RNA polymerase protein previously predicted as a CD8 T cell epitope,5 in keeping with T cell antigen presentation derived from processing both structural and non-structural proteins. The identification of immunogenic coronavirus epitopes with high sequence identity may indicate SARS-CoV-2 targets for vaccine development against COVID-19. Latent exposure to the coronaviridae family might contribute to musculoskeletal autoimmune disease development, as illustrated by a recent report of myositis in a patient with COVID-19.7
Handling editor Josef S Smolen
Contributors Conceptualisation: IH, LH, TDJW, XH, SM, WERO and JAL. Methodology: IH, LH, TDJW, XH and SM. Software: TDJW and XH. Investigation: SM. Resources: IH, LH. Writing-original draft: SM and JAL. Writing-review and editing: SM, TDJW, JAL, IH, LH, XH, WERO and HC. Funding acquisition: JAL, IH, WERO and HC.
Funding This study was supported by a research grant from The Myositis Association. TDJW was supported by a research grant from Children with Cancer and The Caring Cancer Trust. XH was supported by grants from The Humane Research Trust and work in the Viral Oncology Labs was supported by grants from the Cancer Prevention Research Trust. HC and JL were supported by the Medical Research Council (MR/N003322/1). HC was supported by the NIHR Biomedical Research Centre Funding Scheme. The views expressed in this publication are those of the authors and not necessarily those of the NHS, the National Institute for Health Research or the Department of Health.
Competing interests JAL reports grants from The Myositis Association, grants from Medical Research Council (MR/N003322/1), during the conduct of the study; grants from MedImmune, outside the submitted work.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication Not required.
Ethics approval All samples were collected with relevant research ethics committee approval (MREC 98//8/86 North West Haydock Research Ethics Committee for UKMyoNet and UREC 02225 and UREC4 2017-1256-2489 for healthy control cohort).
Provenance and peer review Not commissioned; externally peer reviewed.
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