IL-10 is an anti-inflammatory cytokine which may modulate disease expr
ession in RA. Three dimorphic polymorphisms within the IL-10 gene prom
oter have recently been identified and appear to influence regulation
of its expression. The -1082A allele has been associated with low and
the -1082G allele with high in vitro IL-10 production. We have analy
sed 117 unrelated Caucasoid RA patients and 119 ethnically matched con
trols. No significant differences in the allele frequencies of the thr
ee polymorphisms were found between controls and RA patients. In contr
ast, a significant association between the -1082A allele and the (-10
82A/-819*C/-592*C) haplotype and IgA RF+ve/IgG RF-ve patients was obs
erved. The association of genotypes encoding low IL-10 production with
IgA RF in RA is incompatible with its suggested role in antibody isot
ype switching. IgA RF has been associated with severe RA and may thus
be indirectly correlated with a genotype encoding low IL-10 production
.