Millman I, Scott A W, Halbherr T, Youmans A S, Youmans G P
Infect Immun. 1976 Oct;14(4):929-33. doi: 10.1128/iai.14.4.929-933.1976.
Mycobacterial ribonucleic acid (RNA) and cell wall skeleton fraction isolated from H37Ra caused P-815 mastocytoma regression in DBA/2 mice provided the animals were presensitized with freshly harvested living H37Ra cells. In the absence of presensitization, only the RNA fraction inhibited. Cell wall skeleton fraction, under these conditions, stimulated tumor growth. Cell wall lipids (from H37Ra) added to H37Ra cell wall skeleton fraction did not increase the inhibitory activity of cell wall skeleton fraction alone. Mycobacterial RNA appeared to be an effective inhibitor of P-815 mastocytoma metastases as shown by (i) the inhibition of a second footpad lesion distant from the one treated and (ii) increase in survival time.
从H37Ra分离出的分枝杆菌核糖核酸(RNA)和细胞壁骨架组分可使DBA/2小鼠的P - 815肥大细胞瘤消退,前提是动物先用新鲜收获的活H37Ra细胞进行预致敏。在没有预致敏的情况下,只有RNA组分具有抑制作用。在这些条件下,细胞壁骨架组分刺激肿瘤生长。添加到H37Ra细胞壁骨架组分中的(来自H37Ra的)细胞壁脂质并没有增加单独的细胞壁骨架组分的抑制活性。分枝杆菌RNA似乎是P - 815肥大细胞瘤转移的有效抑制剂,这表现为:(i)对远离治疗部位的第二个足垫病变的抑制,以及(ii)存活时间的延长。