Anti-U11/U12 Antibodies as a Rare but Important Biomarker in Patients with Systemic Sclerosis: A Narrative Review

Author:

Fritzler Marvin J.1,Bentow Chelsea2,Beretta Lorenzo3ORCID,Palterer Boaz4ORCID,Perurena-Prieto Janire5,Sanz-Martínez Maria Teresa5ORCID,Guillen-Del-Castillo Alfredo6ORCID,Marín Ana5ORCID,Fonollosa-Pla Vicent6,Callejas-Moraga Eduardo7,Simeón-Aznar Carmen Pilar6ORCID,Mahler Michael2

Affiliation:

1. Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada

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

3. Scleroderma Unit and (Referral) Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico di Milan, 20122 Milano, Italy

4. Department of Experimental and Clinical Medicine, University of Florence, 50121 Firenze, Italy

5. Department of Immunology, Hospital Universitari Vall d’Hebron, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain

6. Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Hospital Universitari Vall d’Hebron, 08035 Barcelona, Spain

7. Department of Internal Medicine, Hospital Público de Monforte, 27400 Lugo, Spain

Abstract

Anti-nuclear (ANA) are present in approximately 90% of systemic sclerosis (SSc) patients and are key biomarkers in supporting the diagnosis and determining the prognosis of this disease. In addition to the classification criteria autoantibodies for SSc [i.e., anti-centromere, anti-topoisomerase I (Scl-70), anti-RNA polymerase III], other autoantibodies have been associated with important SSc phenotypes. Among them, anti-U11/U12 ribonucleoprotein (RNP) antibodies, also known as anti-RNPC-3, were first reported in a patient with SSc, but very little is known about their association and clinical utility. The U11/U12 RNP macromolecular complex consists of several proteins involved in alternative mRNA splicing. More recent studies demonstrated associations of anti-anti-U11/U12 antibodies with SSc and severe pulmonary fibrosis as well as with moderate to severe gastrointestinal dysmotility. Lastly, anti-U11/U12 autoantibodies have been strongly associated with malignancy in SSc patients. Here, we aimed to summarize the knowledge of anti-U11/U12/RNPC-3 antibodies in SSc, including their seroclinical associations in a narrative literature review.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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