Establishment of an international autoantibody reference standard for human anti-DFS70 antibodies: proof-of-concept study for a novel Megapool strategy by pooling individual specific sera

Author:

Dellavance Alessandra1,Baldo Danielle C.1,Zheng Bing23,Mora Rodrigo A.2,Fritzler Marvin J.4,Hiepe Falk5,Rönnelid Johan6,Satoh Minoru7,Garcia-De La Torre Ignacio8,Wener Mark H.9,Chan Edward K.L.2,Andrade Luis E.C.1011ORCID

Affiliation:

1. Research and Development Division, Fleury Medicine and Health Laboratory , São Paulo , Brazil

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

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

4. Department of Medicine, Cumming School of Medicine , University of Calgary , Calgary , Alberta , Canada

5. Department of Rheumatology and Clinical Immunology , Charité – Universitätmedizin Berlin, Corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health , Berlin , Germany

6. Department of Immunology, Genetics and Pathology , Uppsala University , Uppsala , Sweden

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

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

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

10. Rheumatology Division, Escola Paulista de Medicina , Universidade Federal de São Paulo , Rua Botucatu 740 3° andar , 04023-062 São Paulo , Brazil

11. Immunology Division, Fleury Medicine and Health Laboratory , São Paulo , Brazil

Abstract

Abstract Background International autoantibody standards, traditionally based on material obtained from plasmapheresis of single subjects, represent individual immune response and may not comprehend the heterogeneity of the general population. The anti-DFS70 autoantibody yields a characteristic dense fine speckled (DFS) nuclear pattern on indirect immunofluorescence assay on HEp-2 cells (HEp-2 IFA) and speaks against autoimmunity. We propose a novel strategy for developing autoantibody reference standards, based on stepwise pooling of serum samples from hundreds of individuals with anti-DFS70 antibodies. Methods Within a 2-year period, serum samples were selected from routine HEp-2 IFA according to the following criteria: DFS HEp-2 IFA pattern at titer ≥1:640; anti-DFS70 reactivity in three analyte-specific tests (Western blot [WB], enzyme-linked immunosorbent assay [ELISA] and chemiluminescent immunoassay [CLIA]). Aliquots of individual samples were combined into progressively larger pools with stepwise validation of intermediary pools as for individual samples. Validated intermediary pools were merged into a final pool for lyophilization. Results A total of 741 validated samples yielded a 750 mL final pool that was lyophilized into thousands of 200 μL-aliquots. Reconstituted aliquots yielded the expected anti-DFS70 reactivity in ELISA, CLIA and WB, as well as high-titer DFS HEp-2 IFA pattern. The appropriate anti-DFS70 reactivity of the lyophilized pool was confirmed by seven international expert centers, using HEp-2 IFA, ELISA, WB and immunoprecipitation. Conclusions This proof-of-concept study provides an innovative and efficient strategy to build serum reference standards for autoantibody testing. The anti-DFS70 standard will integrate the panel of standards of Autoantibody Standardization Committee (ASC, www.autoab.org), contributing to education for proper assay validation and interpretation of the DFS pattern and other HEp-2 IFA patterns.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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