We here report the finding that the anti-inflammatory cytokine interle
ukin-10 (IL-10) inhibits motility of B lymphocytes. B cells were induc
ed to display motile morphology and active migration by IL-4. IL-10 in
hibited locomotor responses to IL-4, when B cells of both murine and h
uman origin were used. The inhibitory effect of IL-10 was reversible,
since washing of B cells preincubated in IL-10 restored the ability to
respond to IL-4, Time-course experiments showed that IL-10 did not ha
ve to be present from the very onset of culture, but could be added as
late as 5 hr after initiation. In addition, murine B cells stimulated
with lipopolysaccharide (LPS) showed motile morphology, as well as ce
llular aggregation and proliferation. All these parameters were suppre
ssed by IL-10. However, viability of B cells was not adversely affecte
d by IL-10. Exposure to IL-10 did not result in any changes in the sur
face expression of molecules involved in adhesion, such as CD2, CD11a/
CD18, CD44, CD54 or L-selectin, on B lymphocytes.