Israel E, Beiss B, Wainberg M A
Immunology. 1980 May;40(1):77-85.
PHA and Con A-driven mitogenesis of mouse C3H lymphocytes can be inhibited by co-incubation with a variety of different virus particles. These effects appear independent of infection, and can be obtained using UV-inactivated virus. Viruses may be added to spleen cell cultures as late as 46 h after co-incubation with mitogen, and still achieve significant inhibition of proliferative responsiveness. The described inhibition is apparently mediated, in part at least, by a soluble factor which is induced in splenic cultures following interaction with virus particles. This factor is apparently a product of macrophages. It does not posess interferon activity, but does have the ability to inhibit lectin- and alloantigen-driven mitogenesis, as measured in fresh cultures of splenic lymphocytes and in the mixed lymphocyte culture (MLC) reaction, respectively. Moreover, addition of virus to splenic cultures can apparently activate suppressor lymphocytes with the ability to inhibit proliferative responsiveness of fresh lymphocyte suspensions in the presence of Con A.
通过与多种不同病毒颗粒共同孵育,可抑制PHA和Con A驱动的小鼠C3H淋巴细胞有丝分裂。这些效应似乎与感染无关,使用紫外线灭活病毒也可获得相同结果。病毒可在与促细胞分裂剂共同孵育后长达46小时添加到脾细胞培养物中,仍能显著抑制增殖反应性。所述抑制作用显然至少部分是由一种可溶性因子介导的,该因子是在脾细胞培养物与病毒颗粒相互作用后诱导产生的。这种因子显然是巨噬细胞的产物。它不具有干扰素活性,但确实具有抑制凝集素和同种抗原驱动的有丝分裂的能力,分别在脾淋巴细胞新鲜培养物和混合淋巴细胞培养(MLC)反应中进行测定。此外,向脾细胞培养物中添加病毒显然可以激活抑制性淋巴细胞,这些抑制性淋巴细胞能够在存在Con A的情况下抑制新鲜淋巴细胞悬液的增殖反应性。