Reference standards for the detection of anti-mitochondrial and anti-rods/rings autoantibodies

Author:

Calise S. John1,Zheng Bing1,Hasegawa Tomoko2,Satoh Minoru2,Isailovic Natasa3,Ceribelli Angela3,Andrade Luis E.C.45,Boylan Katherine6,Cavazzana Ilaria7,Fritzler Marvin J.8,de la Torre Ignacio Garcia9,Hiepe Falk10,Kohl Kathryn6,Selmi Carlo311,Shoenfeld Yehuda12,Tincani Angela7,Chan Edward K.L.1

Affiliation:

1. Department of Oral Biology , University of Florida , Gainesville, FL , USA

2. Department of Clinical Nursing , University of Occupational and Environmental Health , Kitakyushu , Japan

3. Laboratory of Autoimmunity and Metabolism , Division of Rheumatology and Clinical Immunology , Humanitas Research Hospital , Rozzano, Milan , Italy

4. Division of Rheumatology, Escola Paulista de Medicina , Universidade Federal de São Paulo , São Paulo , Brazil

5. Immunology Division , Fleury Medicine and Health Laboratories , São Paulo , Brazil

6. Scientific and Clinical Affairs, Plasma Services Group, Inc. , Huntingdon Valley, PA , USA

7. Department of Clinical and Experimental Science , University of Brescia and ASST-Spedali Civili di Brescia , Brescia , Italy

8. Department of Medicine, Cumming School of Medicine , University of Calgary , Calgary , Canada

9. Department of Immunology and Rheumatology , Hospital General de Occidente and University of Guadalajara , Guadalajara , Mexico

10. Charité – Universitätsmedizin Berlin and Deutsches Rheumaforschungszentrum Berlin , Berlin , Germany

11. BIOMETRA Department , University of Milan , Milan , Italy

12. Zabludowicz Center for Autoimmune Diseases, Sheba Medical Center , Tel Hashomer , Israel

Abstract

Abstract Background: Anti-mitochondrial antibodies (AMA) are found in >90% of primary biliary cholangitis patients. Anti-rods/rings antibodies (anti-RR) are most commonly associated with interferon-α and ribavirin treatment in hepatitis C patients. Clinical laboratories routinely screen for AMA and anti-RR using indirect immunofluorescence on HEp-2 cells (HEp-2-IFA). Therefore, we sought to establish reference materials for use in AMA and anti-RR testing. Methods: AMA-positive and anti-RR-positive human plasma samples (AMA-REF and RR-REF), identified as potential reference materials based on preliminary data, were further validated by multiple laboratories using HEp-2-IFA, immunoprecipitation (IP), western blotting, IP-western, line immunoassay (LIA), addressable laser bead immunoassay (ALBIA) and enzyme-linked immunosorbent assay (ELISA). Results: AMA-REF showed a strong positive cytoplasmic reticular/AMA staining pattern by HEp-2-IFA to ≥1:1280 dilution and positive signal on rodent kidney/stomach/liver tissue. AMA-REF reacted with E2/E3, E3BP, E1α and E1β subunits of the pyruvate dehydrogenase complex by IP and western blotting and was positive for AMA antigens by LIA, ALBIA and ELISA. RR-REF showed a strong positive rods and rings staining pattern by HEp-2-IFA to ≥1:1280 dilution. RR-REF reacted with inosine monophosphate dehydrogenase by IP, IP-western and ALBIA. RR-REF also produced a nuclear homogenous staining pattern by HEp-2-IFA, immunoprecipitated proteins associated with anti-U1RNP antibody and reacted weakly with histones, nucleosomes, Sm and nRNP/Sm by LIA. Conclusions: AMA-REF and RR-REF are useful reference materials for academic or commercial clinical laboratories to calibrate and establish internal reference standards for immunodiagnostic assays. AMA-REF and RR-REF are now available for free distribution to qualified laboratories through Plasma Services Group.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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