A crude polysaccharide fraction (DAP-1) was prepared from roots of Dipsacus asperoides by hot water extraction and EtOH precipitation, and tested for anti-complementary activity, mitogenic activity of lymphocytes, and effects on acid phosphatase and phagocytic activities of macrophages. DAP-1 showed not only anti-complementary activity but also a stimulating effect on the mitogenic activity of lymphocytes. DAP-1 also significantly suppressed the phagocytic activity of macrophages.Although DAP-1 directly stimulated the mitogenecity of lymphocytes, it had no effect on lipopolysaccharide-or concanavalin A-induced mitogenic activity of lymphocytes. Periodate oxidation and pronase digestion suggested that the polysaccharide moiety in DAP-1 contributed to the expression of its anticomplementary and mitogenic activities and that the protein moiety in DAP-1 was responsible for its effect on phagocytosis. DAP-1 gave three polysaccharide fractions (DAP-2, 3, and 4) by fractionation using cetyltrimethylammonium bromide. All the fractions had potent anti-complementary activity, but showed different stimulating or suppressive effects on the proliferation of lymphocytes, phagocytosis, or acid phosphatase activity. Three potent anti-complementary polysaccharides (DAP-41-la, DAP-41-lb. and DAP-4lla-1) were purified from DAP-4 by anionexchange chromatography, gel filtration, and HPLC. DAP-4l-la, 1-ib, and ha-i consisted of Ara, Rha, Xyl, Gal, GIc and GIcA in a molar ratio of 1.0:0.7:1.0:18.6:22.2:nil; 1.0:0.1:0.3:19.3 26.8:nil; and 3.7:trace:0.6:26.3:5.5 :1.0; respectively. Among the polysaccharides, only DAP-4lla-1 reacted with /i-glucosylYariv antigen. Methylation analysis indicated that DAP-4l-la mainly comprised 4-linked Gal and 3-, 4-, and 6-linked Glc, whereas DAP-4lla-1 consisted mainly of terminal Araf, 3-linked GIc, and 3,6-branched Gal.