Previous Article | Next Article ![]()
Infection and Immunity, June 1999, p. 2769-2775, Vol. 67, No. 6
Infection and Immunity
Group1 and Biochemistry
Section,
Received 30 November 1998/Returned for modification 12 January
1999/Accepted 3 March 1999
Cross-reactivity or molecular mimicry may be one of the underlying
mechanisms involved in the etiopathogenesis of rheumatoid arthritis
(RA). Antiserum against the RA susceptibility sequence EQKRAA was shown
to bind to a similar peptide ESRRAL present in the hemolysin of the
gram-negative bacterium Proteus mirabilis, and an
anti-ESRRAL serum reacted with EQKRAA. There was no reactivity with
either anti-EQKRAA or anti-ESRRAL to a peptide containing the EDERAA
sequence which is present in HLA-DRB1*0402, an allele not associated
with RA. Furthermore, the EQKRAA and ESRRAL antisera bound to a mouse
fibroblast transfectant cell line (Dap.3) expressing HLA-DRB1*0401
but not to DRB1*0402. However, peptide sequences structurally related
to the RA susceptibility motif LEIEKDFTTYGEE (P. mirabilis
urease), VEIRAEGNRFTY (collagen type II) and DELSPETSPYVKE (collagen
type XI) did not bind significantly to cell lines expressing HLA-DRB1*0401 or HLA-DRB1*0402 compared to the control peptide YASGASGASGAS. It is suggested here that molecular mimicry between HLA
alleles associated with RA and P. mirabilis may be relevant in the etiopathogenesis of the disease.
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Cross-Reactivity between the Rheumatoid Arthritis-Associated
Motif EQKRAA and Structurally Related Sequences Found in
Proteus mirabilis
*
Corresponding author. Mailing address: Infection and
Immunity Group, Division of Life Sciences, King's College, Campden
Hill Rd., London, W8 7AH, United Kingdom. Phone: 0171-333-4302. Fax: 0171-333-4500. E-mail: alan.ebringer{at}kcl.ac.uk.
Infection and Immunity, June 1999, p. 2769-2775, Vol. 67, No. 6
0019-9567/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»