H. Tiwana et al., Cross-reactivity between the rheumatoid arthritis-associated motif EQKRAA and structurally related sequences found in Proteus mirabilis, INFEC IMMUN, 67(6), 1999, pp. 2769-2775
Cross-reactivity or molecular mimicry may be one of the underlying mechanis
ms involved in the etiopathogenesis of rheumatoid arthritis (RA), Antiserum
against the RA susceptibility sequence EQKRAA was shown to bind to a simil
ar peptide ESRRAL present in the hemolysin of the gram-negative bacterium P
roteus mirabilis, and an anti-ESRRAL serum reacted with EQKRAA. There was n
o 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 assoc
iated 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 su
sceptibility motif LEIEKDFTTYGEE (P. mirabilis urease), VEIRAEGNRFTY (colla
gen type II) and DELSPETSPYVKE (collagen type XI) did not bind significantl
y to cell lines expressing HLA-DRB1*0401 or HLA-DRB1*0402 compared to the c
ontrol peptide YASGASGASGAS. It is suggested here that molecular mimicry be
tween HLA alleles associated with RA and P. mirabilis may be relevant in th
e etiopathogenesis of the disease.