Matsubara S, Suzuki M, Nakamura M, Edo K, Ishida N
Cancer Res. 1980 Jul;40(7):2534-8.
A low-molecular-weight fraction (M.W. approximately 700) that specifically impairs the induction of type II interferon in mice by purified protein derivative of tuberculin or OK-432 was isolated from the cell-free ascitic fluid of mice bearing Ehrlich ascites carcinoma. Purification was achieved by ultrafiltration and gel filtration. The inhibitory activity of the isolated fraction was 10 times greater than that of the unfractionated starting material in the impairment of type II interferon induction. The significant inhibition was observed even when 0.2 ml of the 10,000-fold dilution of the fraction, which was previously adjusted to 0.25 A unit at 290 nm absorption, was once treated i.p. in normal mice 48 hr before challenge of type II interferon inducers. This fraction was stable to heating at 56 degrees for 60 min. The active component, however, did not affect the in vivo induction of type I interferon by polyriboinosinic-polyribocytidylic acid or tilorone-HCl. In parallel experiments, an identical low-molecular-weight fraction that impairs the type II interferon induction in mice was isolated from the ascitic fluids of rats bearing AH-100B ascites tumor and from a human hepatoma case with advanced cancer metastatic to the peritoneal cavity. However, nontumorous ascitic fluids obtained from adjuvant-stimulated mice and a human liver cirrhosis case did not contain any such inhibitory activity.
从携带艾氏腹水癌的小鼠无细胞腹水中分离出一种低分子量组分(分子量约为700),该组分可特异性抑制结核菌素纯蛋白衍生物或OK-432对小鼠II型干扰素的诱导。通过超滤和凝胶过滤实现了纯化。在II型干扰素诱导受损方面,分离出的组分的抑制活性比未分级的起始材料高10倍。即使将该组分以10,000倍稀释,取0.2 ml(该稀释液在290 nm吸收波长下预先调整至0.25 A单位),在正常小鼠中于II型干扰素诱导剂攻击前48小时腹腔注射一次,仍观察到显著抑制作用。该组分在56℃加热60分钟仍稳定。然而,活性成分并不影响聚肌苷酸-聚胞苷酸或盐酸泰洛龙在体内诱导I型干扰素。在平行实验中,从携带AH-100B腹水瘤的大鼠腹水中以及从一名晚期癌症转移至腹腔的人类肝癌病例的腹水中,分离出了一种相同的、可损害小鼠II型干扰素诱导的低分子量组分。然而,从佐剂刺激的小鼠获得的非肿瘤性腹水以及一名人类肝硬化病例的腹水均不含有任何此类抑制活性。