Cross reaction of antibodies to a glycine/alanine repeat sequence of Epstein-Barr virus nuclear antigen-1 with collagen, cytokeratin, and actin
- PMID: 1722966
- PMCID: PMC1004556
- DOI: 10.1136/ard.50.11.772
Cross reaction of antibodies to a glycine/alanine repeat sequence of Epstein-Barr virus nuclear antigen-1 with collagen, cytokeratin, and actin
Abstract
P62 is a synthetic peptide which corresponds to the glycine/alanine repeat sequence of Epstein-Barr virus nuclear antigen-1. It is the main epitope recognised by anti-rheumatoid arthritis nuclear antigen antibodies. It was shown previously that anti-P62 antibodies were raised fourfold in patients with rheumatoid arthritis compared with controls. To examine the possibility that this increase was due to cross reactive autoantibodies binding to P62, anti-P62 antibodies from serum samples taken from 10 patients with rheumatoid arthritis and five healthy controls were purified by affinity chromatography. Immunoglobulin G anti-P62 antibodies purified from four of 10 serum samples from patients with rheumatoid arthritis also reacted with human epidermal keratin, denatured collagen type II and actin, but not with influenza antigens, as determined by enzyme linked immunosorbent assay (ELISA). Anti-P62 antibodies in serum samples from healthy controls and patients with rheumatoid arthritis reacted with epidermal keratin by immunoblotting. It is suggested that antibodies to the glycine/alanine repeat sequence of Epstein-Barr nuclear antigen-1 recognise homologous epitopes on keratin, actin, and collagen. It is also possible that molecular mimicry between a major epitope on the Epstein-Barr virus and several autoantigens might contribute to the breakdown of tolerance and autoimmunity in patients with rheumatoid arthritis.
Similar articles
-
Antibodies in rheumatoid arthritis react specifically with the glycine alanine repeat sequence of Epstein-Barr nuclear antigen-1.Rheumatol Int. 1989;9(3-5):161-6. Rheumatol Int. 1989. PMID: 2481875
-
Reaction of antibodies to rheumatoid arthritis nuclear antigen with a synthetic peptide corresponding to part of Epstein-Barr nuclear antigen 1.Ann Rheum Dis. 1988 Apr;47(4):270-9. doi: 10.1136/ard.47.4.270. Ann Rheum Dis. 1988. PMID: 2452607 Free PMC article.
-
Serum IgA cross-reactivity between glycine-alanine repeat sequence of EBNA-1 and keratin or collagen in nasopharyngeal carcinoma.Clin Immunol Immunopathol. 1994 May;71(2):164-8. doi: 10.1006/clin.1994.1067. Clin Immunol Immunopathol. 1994. PMID: 7514112
-
The possible role of Epstein-Barr virus in rheumatoid arthritis.Rev Infect Dis. 1979 Nov-Dec;1(6):997-1006. doi: 10.1093/clinids/1.6.997. Rev Infect Dis. 1979. PMID: 233172 Review.
-
On the etiology of rheumatoid arthritis.Scand J Rheumatol Suppl. 1988;74:19-28. doi: 10.3109/03009748809102935. Scand J Rheumatol Suppl. 1988. PMID: 2852847 Review. No abstract available.
Cited by
-
Epstein-Barr Viruses: Their Immune Evasion Strategies and Implications for Autoimmune Diseases.Int J Mol Sci. 2024 Jul 26;25(15):8160. doi: 10.3390/ijms25158160. Int J Mol Sci. 2024. PMID: 39125729 Free PMC article. Review.
-
Viruses, virulence and pathogenicity.Baillieres Clin Haematol. 1995 Mar;8(1):1-23. doi: 10.1016/s0950-3536(05)80230-6. Baillieres Clin Haematol. 1995. PMID: 7663043 Free PMC article. Review.
-
The cytokeratin filament-aggregating protein filaggrin is the target of the so-called "antikeratin antibodies," autoantibodies specific for rheumatoid arthritis.J Clin Invest. 1993 Sep;92(3):1387-93. doi: 10.1172/JCI116713. J Clin Invest. 1993. PMID: 7690781 Free PMC article.
-
Molecular mimicry in the pathogenesis of autoimmune rheumatic diseases.J Transl Autoimmun. 2025 Jan 7;10:100269. doi: 10.1016/j.jtauto.2025.100269. eCollection 2025 Jun. J Transl Autoimmun. 2025. PMID: 39877080 Free PMC article. Review.
-
Increased serum and synovial fluid antibodies to immunoselected peptides in patients with rheumatoid arthritis.Ann Rheum Dis. 1996 Jul;55(7):437-41. doi: 10.1136/ard.55.7.437. Ann Rheum Dis. 1996. PMID: 8774161 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases