De Maeyer E, De Maeyer-Guignard J
Ann N Y Acad Sci. 1980;350:1-11. doi: 10.1111/j.1749-6632.1980.tb20601.x.
The effect of type I interferon production on immunity to the interferon-inducing virus was examined using the Newcastle disease virus [NDV]-mouse model and comparing If-1h and If-1l animals. The degree of cell-mediated immunity, as measured by delayed hypersensitivity [DH] to NDV, was influenced by the levels of interferon produced. Anti-interferon globulin given immediately after immunization decreased sensitization to NDV, whereas additional, exogenous, interferon, given to low interferon producers, stimulated sensitization to NDV. The alleles at the If-1 locus influenced the extent of DH to NDV, in that If-1h mice developed much stronger DH than did If-1l mice. However, results from recombinant inbred strains, F2 and backcross generations showed that for interferon production to stimulate DH to NDV, other genes, present in the C57BL/6 background but as yet not characterized, are required. Thus DH to NDV is determined on the one hand by the alleles at If-1, influencing interferon production, and on the other hand by a combination of several genes affecting the interaction of interferon with cells of the immune system.
使用新城疫病毒(NDV)-小鼠模型并比较If-1h和If-1l动物,研究了I型干扰素产生对干扰素诱导病毒免疫的影响。通过对NDV的迟发型超敏反应(DH)来衡量的细胞介导免疫程度受干扰素产生水平的影响。免疫后立即给予抗干扰素球蛋白可降低对NDV的致敏性,而给予低干扰素产生者额外的外源性干扰素则刺激对NDV的致敏性。If-1位点的等位基因影响对NDV的DH程度,因为If-1h小鼠产生的DH比If-1l小鼠强得多。然而,重组近交系、F2和回交世代的结果表明,为了使干扰素产生刺激对NDV的DH,需要C57BL/6背景中存在但尚未鉴定的其他基因。因此,对NDV的DH一方面由影响干扰素产生的If-1等位基因决定,另一方面由影响干扰素与免疫系统细胞相互作用的几个基因的组合决定。