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The myositis clinical phenotype associated with anti-Zo autoantibodies: A case series of nine UK patients

Research output: Contribution to journalArticle

Sarah L. Tansley, Zoe Betteridge, Hui Lu, Emma Davies, Simon Rothwell, Paul P. New, Hector Chinoy, Patrick Gordon, Harsha Gunawardena, Mark Lloyd, Richard Stratton, Robert Cooper, Neil J. McHugh

Original languageEnglish
Pages (from-to)1626-1631
Number of pages6
JournalRheumatology (United Kingdom)
Issue number7
Published1 Jul 2020

King's Authors


It has been over 10 years since the first report of autoantibodies directed against phenylalanyl tRNA synthetase (anti-Zo) in a patient with features of the anti-synthetase syndrome. In that time no further cases have been published. Here we aim to characterize more fully the clinical phenotype of anti-Zo-associated myositis by describing the clinical features of nine patients. Methods: Anti-Zo was identified by protein-immunoprecipitation in patients referred for extended spectrum myositis autoantibody testing at our laboratory. Results were confirmed by immunodepletion using a reference serum. Medical records were retrospectively reviewed to provide detailed information of the associated clinical phenotype for all identified patients. Where possible, HLA genotype was imputed using Illumina protocols. Results: Nine patients with anti-Zo were identified. The median age at disease onset was 51 years, and six patients were female. Seven patients had evidence of inflammatory muscle disease, seven of interstitial lung disease and six of arthritis. The reported pattern of interstitial lung disease varied with usual interstitial pneumonia, non-specific interstitial pneumonia and organizing pneumonia all described. Other features of the anti-synthetase syndrome such as RP and mechanics hands were common. HLA data was available for three patients, all of whom had at least one copy of the HLA 8.1 ancestral haplotype. Conclusion: Patients with anti-Zo presenting with features of the anti-synthetase syndrome and interstitial lung disease is a common finding. Like other myositis autoantibodies, there is likely to be a genetic association with the HLA 8.1 ancestral haplotype.

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