Baldwin Susan L, Powell Tim D, Sellins Karen S, Radecki Steven V, Cohen J John, Milhausen Michael J
Heska Corporation, 1613 Prospect Parkway, Fort Collins, CO 80525, USA.
Vet Immunol Immunopathol. 2004 Jun;99(3-4):153-67. doi: 10.1016/j.vetimm.2004.01.012.
IFN-alpha has been shown to induce both antiviral and antiproliferative activities in animals. This report describes the biological activity of five recently identified feline IFN-alpha subtypes expressed in the Chinese hamster ovary (CHO) cell line (rfeIFN-alpha1[CHO], rfeIFN-alpha2[CHO], rfeIFN-alpha3[CHO], rfeIFN-alpha5[CHO] and rfeIFN-alpha6[CHO]) and the feIFN-alpha6 subtype expressed in and purified from Pichia pastoris (rfeIFN-alpha6[P. pastoris]). The rfeIFN-alpha[CHO] subtypes were tested for antiviral activity against either Vesicular stomatitis virus (VSV) or feline calicivirus (FCV) infected feline embryonic fibroblast cell line (AH927) or Crandell feline kidney cell line (CRFK). Antiviral activity was induced against both VSV and FCV infected AH927 cells and VSV infected CRFK cells by all five of the rfeIFN-alpha[CHO] subtypes and rfeIFN-alpha6[P. pastoris]. In addition, the IFN-alpha inducible Mx gene (associated with antiviral activity) was upregulated in vivo 24 h following treatment with rfeIFN-alpha6[P. pastoris], compared to baseline levels seen prior to treatment. All of the rfeIFN-alpha[CHO] subtypes and rfeIFN-alpha6[P. pastoris] exhibited antiproliferative activity in the FeT-J cell line (an IL-2 independent feline T-cell line). Both necrosis and apoptosis were observed in rfeIFN-alpha6[P. pastoris]-treated FeT-J cells. The rfeIFN-alpha3[CHO] subtype consistently exhibited lower antiviral and antiproliferative activity compared to that observed with the other four rfeIFN-alpha[CHO] subtypes. In summary, this paper demonstrates that five previously described feIFN-alpha subtypes induce both antiviral and antiproliferative activities in vitro and are capable of upregulating the feMx gene in vivo.
干扰素-α已被证明在动物体内具有抗病毒和抗增殖活性。本报告描述了最近鉴定出的五种在中国仓鼠卵巢(CHO)细胞系中表达的猫干扰素-α亚型(rfeIFN-α1[CHO]、rfeIFN-α2[CHO]、rfeIFN-α3[CHO]、rfeIFN-α5[CHO]和rfeIFN-α6[CHO])以及在毕赤酵母中表达并纯化的feIFN-α6亚型(rfeIFN-α6[毕赤酵母])的生物学活性。对rfeIFN-α[CHO]亚型针对水疱性口炎病毒(VSV)或猫杯状病毒(FCV)感染的猫胚胎成纤维细胞系(AH927)或克兰德尔猫肾细胞系(CRFK)进行抗病毒活性测试。所有五种rfeIFN-α[CHO]亚型和rfeIFN-α6[毕赤酵母]均对VSV和FCV感染的AH927细胞以及VSV感染的CRFK细胞诱导出抗病毒活性。此外,与治疗前的基线水平相比,用rfeIFN-α6[毕赤酵母]治疗后24小时,体内干扰素-α诱导的Mx基因(与抗病毒活性相关)上调。所有rfeIFN-α[CHO]亚型和rfeIFN-α6[毕赤酵母]在FeT-J细胞系(一种白细胞介素-2非依赖性猫T细胞系)中均表现出抗增殖活性。在用rfeIFN-α6[毕赤酵母]处理的FeT-J细胞中观察到坏死和凋亡。与其他四种rfeIFN-α[CHO]亚型相比,rfeIFN-α3[CHO]亚型始终表现出较低的抗病毒和抗增殖活性。总之,本文证明了五种先前描述的feIFN-α亚型在体外诱导抗病毒和抗增殖活性,并能够在体内上调feMx基因。