Sakurai H, Takei Y, Omata Y, Suzuki N
Zentralbl Bakteriol Mikrobiol Hyg A Med Mikrobiol Infekt Parasitol. 1981 Dec;251(1):134-43.
Assessment in vitro were carried out to study Toxo-GIF and IFN in lymphokines, LKs, produced by immune spleen cells with Toxoplasma lysate antigen (TLA). LKs were obtained from the cells after incubation for 24 to 48 h with TLA. They inhibited almost completely the intracellular multiplication of Toxoplasma (Tp) within homologous cells. Peak IFN activities were observed in the same LKs. The IFN was inactivated at pH 2, but did not lose its activity at 56 degrees C, suggesting that it might be type II or gamma IFN. Further evidence was presented of the coordinate production and properties of Toxo-GIF and IFN in the circulating blood of Tp-immune mice injected intraperitoneally with TLA or Poly I: C. The IFN was designated type II or gamma IFN. Its maximum activity appeared in Tp-immune mice 6 h after TLA or Poly I: C injection, while a maximum Toxo-GIF activity was observed in these mice 24 to 48 h after injection. Type I IFN activity was detected in the serum of normal mice injected with TLA or Poly I: C. Type I IFN differed markedly from type II IFN, because it was stable at pH 2 and unstable at 56 degrees C. Evidence was presented which emphasized the difference in activity in relation to the time of appearance between Toxo-GIF and IFN.
进行体外评估以研究弓形虫生长抑制因子(Toxo - GIF)和免疫脾细胞与弓形虫裂解物抗原(TLA)产生的淋巴因子(LKs)中的干扰素(IFN)。LKs是细胞与TLA孵育24至48小时后获得的。它们几乎完全抑制了同源细胞内弓形虫(Tp)的细胞内增殖。在相同的LKs中观察到了IFN活性峰值。该IFN在pH 2时失活,但在56℃时不失活,这表明它可能是II型或γ干扰素。进一步的证据表明,在腹腔注射TLA或聚肌胞苷酸(Poly I:C)的Tp免疫小鼠的循环血液中,Toxo - GIF和IFN具有协同产生和特性。该IFN被指定为II型或γ干扰素。其最大活性在TLA或Poly I:C注射后6小时出现在Tp免疫小鼠中,而在这些小鼠注射后24至48小时观察到最大的Toxo - GIF活性。在注射TLA或Poly I:C的正常小鼠血清中检测到I型IFN活性。I型IFN与II型IFN明显不同,因为它在pH 2时稳定,在56℃时不稳定。有证据强调了Toxo - GIF和IFN在活性出现时间方面的差异。