In fact, the expression of Fcγ receptor type I (FcγRI; CD64) and FcγRII (CD32) on circulating monocytes was enhanced after IL-10 treatment in patients with RA, and the in vitro study showed that IL-10-primed monocytes with high-level expression of FcγRI and FcγRII are able to produce TNF-α in response to immune complexes [18]. This evidence concerns the gene TNF and rheumatoid arthritis.