S. Albani et al., IMMUNE-RESPONSES TO THE ESCHERICHIA-COLI DNAJ HEAT-SHOCK PROTEIN IN JUVENILE RHEUMATOID-ARTHRITIS AND THEIR CORRELATION WITH DISEASE-ACTIVITY, The Journal of pediatrics, 124(4), 1994, pp. 561-565
Patients with juvenile rheumatoid arthritis frequently have abnormal i
mmune responses to the hsp65 class of bacterial heat shock proteins. H
owever, lymphocytes from children with other inflammatory diseases may
also recognize hsp65, and the role of these antigens in juvenile rheu
matoid arthritis remains controversial. We have studied humoral and ce
llular immune responses to a distinct, recently described bacterial he
at shock protein, designated dnaJ. The Escherichia coli dnaJ gene was
cloned and expressed, and the purified recombinant protein was used as
an antigen. Neither normal children nor children with various chronic
inflammatory diseases had lymphocyte proliferative responses to recom
binant dnaJ. However, lymphocytes from patients with polyarticular, pa
uciarticular, and systemic manifestations of juvenile rheumatoid arthr
itis responded strongly to the antigen. Cellular immune responses to d
naJ were higher in synovial fluid than in blood and higher in children
with active disease than in children in remission. These data show th
at increased immune reactivity to dnaJ is characteristic of juvenile r
heumatoid arthritis and that the magnitude of the immune response is l
inked to disease activity. The results suggest that an abnormal immune
response to antigens on commensal gut bacteria may contribute to the
generation of chronic inflammation in juvenile rheumatoid arthritis.