Protein arrays for autoantibody profiling and fine‐specificity mapping
- 27 October 2003
- journal article
- review article
- Published by Wiley in Proteomics
- Vol. 3 (11) , 2077-2084
- https://doi.org/10.1002/pmic.200300583
Abstract
Protein arrays provide a powerful approach to study autoimmune disease. Autoimmune responses activate B cells to produce autoantibodies that recognize self‐molecules termed autoantigens, many of which are proteins or protein complexes. Protein arrays enable profiling of the specificity of autoantibody responses against panels of peptides and proteins representing known autoantigens as well as candidate autoantigens. In addition to identifying autoantigens and mapping immunodominant epitopes, proteomic analysis of autoantibody responses will further enable diagnosis, prognosis, and tailoring of antigen‐specific tolerizing therapy.Keywords
This publication has 51 references indexed in Scilit:
- The Role of Subclass Switching in the Pathogenesis of Endemic Pemphigus FoliaceusJournal of Investigative Dermatology, 2003
- Proteomics for the Development of DNA Tolerizing Vaccines to Treat Autoimmune DiseaseClinical Immunology, 2002
- Microarrayed allergen molecules: diagnostic gatekeepers for allergy treatmentThe FASEB Journal, 2002
- Global Analysis of Protein Activities Using Proteome ChipsScience, 2001
- Combination of Gene Delivery and DNA Vaccination to Protect from and Reverse Th1 Autoimmune Disease via Deviation to the Th2 PathwayImmunity, 2001
- Citrulline is an essential constituent of antigenic determinants recognized by rheumatoid arthritis-specific autoantibodies.Journal of Clinical Investigation, 1998
- Functional diversity of helper T lymphocytesNature, 1996
- Phenotypic Analysis of Antigen-Specific T LymphocytesScience, 1996
- Functional evidence for epitope spreading in the relapsing pathology of experimental autoimmune encephalomyelitis.The Journal of Experimental Medicine, 1995
- Antibody production to the nucleocapsid and envelope of the hepatitis B virus primed by a single synthetic T cell siteNature, 1987