Chu D T, Lin J R, Wong W
Cancer Hospital, Chinese Academy of Medical Sciences, Beijing.
Zhonghua Zhong Liu Za Zhi. 1994 May;16(3):167-71.
The in vitro induction of LAK cell activity was studied in cancer and AIDS patients. F3, an immuno-regulatory component of Astragalus membranaceus was shown capable of potentiating the LAK cell inducing activity of rIL-2. The killing activity against Hs294T melanoma cell line of LAK cells induced by 50 U/ml rIL-2 in the presence of F3 (55 micrograms/ml) reached 64% which was comparable to that (60%) induced by 500 u/ml of rIL-2 alone. With F3 plus rIL-2, the effector to target cell ratio could be reduced to one-half in order to obtain an equivalent level of cytotoxicity when rIL-2 was used alone. In some patients, whose peripheral blood lymphocytes were relatively inert to rIL-2, F3 could make them responsive to rIL-2. These results imply that F3 may be useful to potentiate LAK cell activity, reduce the amount of rIL-2 and thus minimize the later's toxic side effects when used in vivo.
对癌症患者和艾滋病患者的LAK细胞活性的体外诱导进行了研究。黄芪的免疫调节成分F3显示能够增强重组白细胞介素-2(rIL-2)诱导LAK细胞的活性。在存在F3(55微克/毫升)的情况下,50单位/毫升的rIL-2诱导的LAK细胞对Hs294T黑色素瘤细胞系的杀伤活性达到64%,这与单独使用500单位/毫升rIL-2诱导的杀伤活性(60%)相当。使用F3加rIL-2时,为了获得与单独使用rIL-2时相当的细胞毒性水平,效应细胞与靶细胞的比例可降低至二分之一。在一些外周血淋巴细胞对rIL-2相对不敏感的患者中,F3可使它们对rIL-2产生反应。这些结果表明,F3可能有助于增强LAK细胞活性,减少rIL-2的用量,从而在体内使用时将其毒副作用降至最低。