Gresser I, Bourali C, Lévy J P, Fontaine-Brouty-Boyé D, Thomas M T
Proc Natl Acad Sci U S A. 1969 May;63(1):51-7. doi: 10.1073/pnas.63.1.51.
Repeated administration of potent mouse interferon preparations increased the survival of Balb/c and C 57/B1(6) mice inoculated with 2,000-3,000 RC(19) and EL(4) tumor cells. Only 7/188 (3.7%) untreated mice (or mice treated with control preparations) survived more than 22 days after intraperitoneal inoculation of RC(19) tumor cells. None survived more than 60 days. In contrast, 101/103 (98%) interferon-treated mice survived beyond 22 days, and sixteen (15%) survived more than 60 days. None of these 16 surviving mice show any sign of tumor at present. Three mice (of the 16) from an early experiment are alive ten months after inoculation of RC(19) tumor cells. Mouse interferon preparations derived from three different tissue sources- brain, serum, and monolayer cell cultures (with Newcastle disease virus and West Nile virus as interferon-inducing agents)-all proved effective. A purified preparation of mouse brain interferon was as effective as crude brain interferon. Human amniotic membrane interferon and control tissue preparations were without effect. These findings suggest that interferon itself (or a factor closely associated with interferon) is the active moiety in these preparations.
多次给予强效小鼠干扰素制剂可提高接种2000 - 3000个RC(19)和EL(4)肿瘤细胞的Balb/c和C 57/B1(6)小鼠的存活率。在腹腔接种RC(19)肿瘤细胞后,未经治疗的小鼠(或用对照制剂治疗的小鼠)中只有7/188(3.7%)存活超过22天。没有一只存活超过60天。相比之下,接受干扰素治疗的小鼠中有101/103(98%)存活超过22天,16只(15%)存活超过60天。目前这16只存活小鼠均未表现出任何肿瘤迹象。早期实验中的3只(共16只)小鼠在接种RC(19)肿瘤细胞10个月后仍然存活。源自三种不同组织来源——脑、血清和单层细胞培养物(以新城疫病毒和西尼罗河病毒作为干扰素诱导剂)的小鼠干扰素制剂均证明有效。纯化的小鼠脑干扰素制剂与粗制脑干扰素一样有效。人羊膜干扰素和对照组织制剂无效。这些发现表明干扰素本身(或与干扰素密切相关的一种因子)是这些制剂中的活性成分。