Anti-RuvBL1/2 Autoantibodies Detection in a Patient with Overlap Systemic Sclerosis and Polymyositis

Author:

Di Pietro Linda1ORCID,Chiccoli Fabio1,Salvati Lorenzo12ORCID,Vivarelli Emanuele13,Vultaggio Alessandra13,Matucci Andrea3,Bentow Chelsea4,Mahler Michael4,Parronchi Paola15ORCID,Palterer Boaz1

Affiliation:

1. Department of Experimental and Clinical Medicine, University of Florence, Largo Brambilla, 3, 50121 Firenze, Italy

2. Allergology and Clinical Immunology Unit, Azienda Usl Toscana Sud Est, San Donato Hospital, 52100 Arezzo, Italy

3. Immunoallergology Unit, Careggi University Hospital, 50134 Firenze, Italy

4. Research and Development, Autoimmunity, Werfen, Autoimmunity Headquarters and Technology Center, San Diego, CA 92131-1638, USA

5. Immunology and Cell Therapy Unit, Careggi University Hospital, 50134 Firenze, Italy

Abstract

Anti-RuvBL1/2 autoantibodies have recently been detected in patients with systemic sclerosis (SSc) and scleromyositis overlap syndromes. These autoantibodies exhibit a distinct speckled pattern in an indirect immunofluorescent assay on Hep-2 cells. We report the case of a 48 year old man with facial changes, Raynaud’s phenomenon, puffy fingers, and muscle pain. A speckled pattern on Hep-2 cells was identified, but the conventional antibody testing was negative. Based on the clinical suspicion and the ANA pattern, further testing was sought demonstrating anti-RuvBL1/2 autoantibodies. Hence, a review of the English literature was performed to define this newly emerging clinical–serological syndrome. With the one here reported, a total of 52 cases have been described to date (December 2022). Anti-RuvBL1/2 autoantibodies are highly specific for SSc and are associated with SSc/PM overlaps. Apart from myopathy, gastrointestinal and pulmonary involvement are frequently observed in these patients (94% and 88%, respectively).

Publisher

MDPI AG

Subject

Drug Discovery,Immunology,Immunology and Allergy

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