Hamuro J, Hadding U, Bitter-Suermann D
Immunology. 1978 Apr;34(4):695-705.
The efficiency of some anti-tumour polysaccharides, such as lentinan, pachyman, pachymaran, carboxymethylpachymaran and hydroxyethylpachyman to trigger the alternative pathway of complement activation (APC) was investigated in detail, in order to clarify whether solid phase activation of APC by these polysaccharides will occur or not. From the eight polysaccharides tested, all were found to be potent activators of the alternative pathway except for carboxymethylpachymaran, regardless of their potency of inhibition of sarcoma 180 (S 180) transplanted in mice. This activation was observed both for the insoluble as well as the soluble part of the same polysaccharide. The turnover of C3, C5 and factor B showed no difference among these seven active polysaccharides. The polysaccharide particles (PX), isolated after treatment with C4d GPS showed prominent C3 consuming activity, which disappeared during prolonged incubation at 37 degrees. The activity of the decayed enzyme could be regenerated by treatment with the purified factor B. The stability of the particulate enzyme PX was comparable to the zymosan-complex (ZX) previously described.
详细研究了一些抗肿瘤多糖,如香菇多糖、茯苓聚糖、茯苓多糖、羧甲基茯苓多糖和羟乙基茯苓多糖触发补体激活替代途径(APC)的效率,以阐明这些多糖是否会发生APC的固相激活。在所测试的八种多糖中,发现除羧甲基茯苓多糖外,所有多糖都是替代途径的有效激活剂,无论它们对移植到小鼠体内的肉瘤180(S 180)的抑制效力如何。对于同一种多糖的不溶性部分和可溶性部分均观察到这种激活。在这七种活性多糖中,C3、C5和B因子的周转没有差异。用C4d GPS处理后分离得到的多糖颗粒(PX)表现出显著的C3消耗活性,该活性在37℃长时间孵育过程中消失。通过用纯化的B因子处理可以使衰变酶的活性再生。颗粒酶PX的稳定性与先前描述的酵母聚糖复合物(ZX)相当。