Villinger F, Brar S S, Mayne A, Chikkala N, Ansari A A
Department of Pathology, Emory University School of Medicine, Atlanta, GA 30322, USA.
J Immunol. 1995 Oct 15;155(8):3946-54.
Two major issues severely limit the studies of human recombinant cytokines/growth factors in nonhuman primates. First, assays and reagents specific for the detection and quantitation of human cytokines do not all function when utilized to detect/quantitate the nonhuman primate cytokines. Second, although most of the human cytokines appear to induce similar, if not identical, biologic function when used with cells from nonhuman primates in vitro or in vivo, they invariably induce Ab responses in vivo, precluding their repeated and/or continued use in vivo. Our laboratory has thus initiated studies to clone, sequence, and prepare recombinant cytokines from nonhuman primates and to define assays and reagents for their detection and quantitation at the nucleic acid and protein level. The data that were derived from such studies show that the nonhuman primate cytokines IL-1 alpha, IL-1 beta, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12 alpha, IL-12 beta, IL-15, IFN-alpha, IFN-gamma, and TNF-alpha share 93 to 99% homology at the nucleic acid and protein level with the human equivalents. The most prominent differences between human and nonhuman primate cytokine sequences were noted for IL-1 alpha/beta, IL-2, IL-8, IFN-alpha, IFN-gamma, and IL-12 beta. The aligned sequences of cytokines for human and several nonhuman primate species are provided herein, and a phylogenetic analysis of the published sequences of select cytokines from other species, along with those of the nonhuman primates, are described. In addition, comparative analysis of the relative bioactivity of our immunoaffinity-purified recombinant rhesus macaque IL-4, IL-15, and IFN-gamma with commercially available human recombinant cytokines is described herein.
两个主要问题严重限制了在非人类灵长类动物中对人类重组细胞因子/生长因子的研究。第一,用于检测和定量人类细胞因子的特异性检测方法和试剂,在用于检测/定量非人类灵长类动物细胞因子时并非都能发挥作用。第二,尽管大多数人类细胞因子在体外或体内与非人类灵长类动物的细胞一起使用时,似乎能诱导相似(即便不是完全相同)的生物学功能,但它们在体内总会诱导抗体反应,这使得它们无法在体内重复和/或持续使用。因此,我们实验室已启动研究,以克隆、测序并制备来自非人类灵长类动物的重组细胞因子,并确定在核酸和蛋白质水平检测和定量它们的检测方法和试剂。这些研究得出的数据表明,非人类灵长类动物的细胞因子白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)、白细胞介素-12α(IL-12α)、白细胞介素-12β(IL-12β)、白细胞介素-15(IL-15)、干扰素-α(IFN-α)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)在核酸和蛋白质水平与相应的人类细胞因子具有93%至99%的同源性。人类和非人类灵长类动物细胞因子序列之间最显著的差异见于IL-1α/β、IL-2、IL-8、IFN-α、IFN-γ和IL-12β。本文提供了人类和几种非人类灵长类动物物种细胞因子的比对序列,并描述了对来自其他物种以及非人类灵长类动物的选定细胞因子已发表序列的系统发育分析。此外,本文还描述了我们免疫亲和纯化的重组恒河猴IL-4、IL-15和IFN-γ与市售人类重组细胞因子相对生物活性的比较分析。