Objective. Interleukin-10 (IL-10) has been shown to exert both antiinf
lammatory and immunostimulatory effects in vivo and in vitro. We there
fore sought to examine the role of this cytokine in rheumatoid arthrit
is (RA) by assessing serum and synovial fluid IL-10 levels. Methods. S
erum and synovial fluid samples were collected from patients with RA a
nd patients with various inflammatory, infectious, and noninflammatory
arthritides (controls). IL-10 was assayed using an IL-10-specific enz
yme-linked immunosorbent assay, and messenger RNA (mRNA) levels were a
ssessed by semiquantitative polymerase chain reaction (PCR) techniques
. Results. Both RA serum and synovial fluid contained significantly el
evated IL-10 levels compared with levels in normal subjects or in cont
rol patients (P < 0.01). Some patients with spondylarthropathy also ma
nifested increased serum levels of IL-10. Serum levels of IL-10 did no
t correlate with standard measures of clinical activity, but were show
n to correlate significantly with serum rheumatoid factor (RF) titers
and in vitro levels of spontaneous IgM-RF production (P < 0.05). PCR a
nalyses demonstrated the constitutive expression of IL-10 mRNA by the
non-T cell population, and semiquantitative PCR analysis documented el
evated levels of IL-10 mRNA in circulating mononuclear cells of those
RA patients who were not treated with slow-acting antirheumatic drugs.
Analysis of IL-10 mRNA revealed the cytokine to be of human, and not
viral, origin. Conclusion. These data suggest that there is increased
production of IL-10 by non-T cells in patients with RA. This may contr
ibute to the diminished T cell function and increased antibody and RF
production in these patients.