THE mutual correlation among soluble CD4 (sCD4), soluble CD8 (sCD8), a
nd soluble CD23 (sCD23) has not yet been studied in patients with rheu
matoid arthritis (RA), although previous studies have demonstrated tha
t certain soluble markers of immune activation are elevated in Rk Thus
, we examined this correlation based on the serum levels of sCD4, sCD8
and sCD23, and that of their levels with other serum markers such as
immunoglobulin (Ig) subtypes (IgG, IgM and IgA), IgM-rheumatoid factor
(IgM-RF) and C-reactive protein (CRP) in 25 RA patients. sCD4 was not
elevated, whereas both sCD8 and sCD23 increased in RA patients compar
ed with the healthy controls; a majority of RA patients, in particular
, showed a high sCD23 level. The level of sCD23 showed a correlation w
ith that of IgM-RF, but not with those of IgG, IgM, IgA and CRP. Impor
tantly, a high level of sCD23 was not always accompanied with that of
sCD8. The independent change between sCD23 and sCD8 levels was also ob
served in a one-year follow-up study of the two RA patients. These fin
dings indicate that B cells might be generally activated in RA, wherea
s T-cell activation in variable in each patient with RA, suggesting th
at sCD23 is a more indicative marker for the immune status of RA patie
nts than sCD8 from the clinical aspects.