Delivery of the sulfated polysaccharide dextrin 2-sulfate by the intraperit
oneal route to the lymphatic circulation resulted in a clinically significa
nt improvement in Kaposi's sarcoma in three patients. Our in vitro studies
show that although sulfated dextrins do not interfere with the growth of is
olated human umbilical vein endothelial cells, they do inhibit the morpholo
gical differentiation of endothelial cells into tubes as well as reduce nem
vessel formation in a placental angiogenesis assay. The antiangiogenic eff
ect of dextrin 6-sulfate is greater than that of dextrin 2-sulfate and is i
ndependent of their anti-human immunodeficiency virus type 1 activities.