Establishment of international autoantibody reference standards for the detection of autoantibodies directed against PML bodies, GW bodies, and NuMA protein

Author:

Zheng Bing12,Mora Rodrigo A.1,Fritzler Marvin J.3,Satoh Minoru4,Bloch Donald B.5,Garcia-De La Torre Ignacio6,Boylan Katherine7,Kohl Kathryn7,Wener Mark H.8,Andrade Luis E. C.910ORCID,Chan Edward K. L.1ORCID

Affiliation:

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

2. Department of Laboratory Medicine, Renji Hospital, School of Medicine , Shanghai Jiao Tong University , Shanghai , PR China

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

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

5. Division of Rheumatology, Allergy and Immunology, Department of Medicine , Massachusetts General Hospital and Harvard Medical School , Boston , MA , USA

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

7. Scientific & Clinical Affairs, Plasma Services Group Inc. , Huntingdon Valley , PA , USA

8. Division of Rheumatology and Department of Laboratory Medicine, University of Washington , Seattle , WA , USA

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

10. Immunology Division , Fleury Laboratories , São Paulo , Brazil

Abstract

Abstract Objectives Reference materials are important in the standardization of autoantibody testing and only a few are freely available for many known autoantibodies. Our goal was to develop three reference materials for antibodies to PML bodies/multiple nuclear dots (MND), antibodies to GW bodies (GWB), and antibodies to the nuclear mitotic apparatus (NuMA). Methods Reference materials for identifying autoantibodies to MND (MND-REF), GWB (GWB-REF), and NuMA (NuMA-REF) were obtained from three donors and validated independently by seven laboratories. The sera were characterized using indirect immunofluorescence assay (IFA) on HEp-2 cell substrates including two-color immunofluorescence using antigen-specific markers, western blot (WB), immunoprecipitation (IP), line immunoassay (LIA), addressable laser bead immunoassay (ALBIA), enzyme-linked immunosorbent assay (ELISA), and immunoprecipitation–mass spectrometry (IP-MS). Results MND-REF stained 6–20 discrete nuclear dots that colocalized with PML bodies. Antibodies to Sp100 and PML were detected by LIA and antibodies to Sp100 were also detected by ELISA. GWB-REF stained discrete cytoplasmic dots in interphase cells, which were confirmed to be GWB using two-color immunofluorescence. Anti-Ge-1 antibodies were identified in GWB-REF by ALBIA, IP, and IP-MS. All reference materials produced patterns at dilutions of 1:160 or greater. NuMA-REF produced fine speckled nuclear staining in interphase cells and staining of spindle fibers and spindle poles. The presence of antibodies to NuMA was verified by IP, WB, ALBIA, and IP-MS. Conclusions MND-REF, GWB-REF, and NuMA-REF are suitable reference materials for the corresponding antinuclear antibodies staining patterns and will be accessible to qualified laboratories.

Funder

JSPS KAKENHI

Canadian Institutes of Health Research

Mexican National Research System

Conacyt

NIH

Bio-Rad

BioSystems

Trinity Biotech

Aesku Group

Euroimmun/Perkin Elmer AG

Inova Diagnostics

Thermo Fisher Scientific

Medical and Biological Laboratories Co.

ImmunoConcepts

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

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