4.8 Article

Autoantigen microarrays for multiplex characterization of autoantibody responses

Journal

NATURE MEDICINE
Volume 8, Issue 3, Pages 295-301

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nm0302-295

Keywords

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Funding

  1. NIAID NIH HHS [K08 AI01521] Funding Source: Medline
  2. NIAMS NIH HHS [K08 AR02133] Funding Source: Medline
  3. NIDDK NIH HHS [U19 DK61934, U19DK61934] Funding Source: Medline
  4. NINDS NIH HHS [5R01NS18235] Funding Source: Medline
  5. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [K08AI001521] Funding Source: NIH RePORTER
  6. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [K08AR002133] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [U19DK061934] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS018235] Funding Source: NIH RePORTER

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We constructed miniaturized autoantigen arrays to perform large-scale multiplex characterization of autoantibody responses directed against structurally diverse autoantigens, using submicroliter quantities of clinical samples. Autoantigen microarrays were produced by attaching hundreds of proteins, peptides and other biomolecules to the surface of derivatized glass slides using a robotic arrayer. Arrays were incubated with patient serum, and spectrally resolvable fluorescent labels were used to detect autoantibody binding to specific autoantigens on the array. We describe and characterize arrays containing the major autoantigens in eight distinct human autoimmune diseases, including systemic lupus erythematosus and rheumatoid arthritis. This represents the first report of application of such technology to multiple human disease sera, and will enable validated detection of antibodies recognizing autoantigens including proteins, peptides, enzyme complexes, ribonucleoprotein complexes, DNA and post-translationally modified antigens. Autoantigen microarrays represent a powerful tool to study the specificity and pathogenesis of autoantibody responses, and to identify and define relevant autoantigens in human autoimmune diseases.

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