Johnston M D
J Gen Virol. 1981 Sep;56(Pt 1):175-84. doi: 10.1099/0022-1317-56-1-175.
The capacity of an egg-grown Sendai virus preparation to induce interferon in the human lymphoblastoid cell Namalwa is dependent on its passage history. Virus which has been serially passaged at high dilution is a poor inducer, whereas virus serially passaged undiluted is a good inducer. Such a good induce preparation has a low infectivity to haemagglutination ratio as the result of a high content of defective-interfering (DI) particles. Using DI particles purified on glycerol gradients, it is shown that for the induction of maximum interferon titres both infectious and DI particles are required. DI particles alone induce little or no interferon. Addition of DI particles to fully infectious Sendai virus preparations increased the interferon yield obtained from Namalwa cells some 60- to 100-fold.
在人淋巴母细胞Namalwa中,鸡胚培养的仙台病毒制剂诱导干扰素的能力取决于其传代历史。在高稀释度下连续传代的病毒是一种较差的诱导剂,而未稀释连续传代的病毒则是一种良好的诱导剂。由于缺陷干扰(DI)颗粒含量高,这种良好的诱导制剂具有低感染性与血凝比。使用在甘油梯度上纯化的DI颗粒表明,为了诱导产生最大干扰素滴度,感染性颗粒和DI颗粒都是必需的。单独的DI颗粒几乎不诱导或不诱导干扰素。向完全感染性的仙台病毒制剂中添加DI颗粒,可使从Namalwa细胞获得的干扰素产量提高约60至100倍。