Li Zhongxia, Phadke Anagha, Weaver Eric A, Ball Judith M, Collisson Ellen W
Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A & M University, College Station, TX 77843, USA.
Dev Comp Immunol. 2005;29(9):809-24. doi: 10.1016/j.dci.2005.01.003. Epub 2005 Feb 24.
Feline immunodeficiency virus (FIV) infection in cats is the only non-primate, small animal model for HIV-AIDS. Replication of FIV has been shown to be optimally suppressed by soluble factors produced by inducer cell-stimulated feline CD8+ cells from FIV-infected cats. The nature of this dose-dependent suppression of FIV was examined. Antiviral factors, produced in serum-free medium, were shown to be either heat stable or heat labile. Suppressing activity was identified in a heparin-bound fraction and the non-bound fraction and in fractions separated by reverse-phase HPLC. The FIV suppression could not be correlated with IFN type I or II. Neither alpha nor beta chemokines were likely candidates because molecular size exclusion centrifugation indicated that the major factors were larger than 50 kD. Identified qualitative differences in the properties of the soluble suppressive activity generated from feline lymphocytes indicated that multiple factors are responsible for the non-cytolytic CD8+ T cell suppression of FIV replication.
猫免疫缺陷病毒(FIV)感染猫是唯一的非灵长类小动物艾滋病模型。已证明来自FIV感染猫的诱导细胞刺激的猫CD8 +细胞产生的可溶性因子能最佳地抑制FIV复制。研究了这种FIV剂量依赖性抑制的性质。在无血清培养基中产生的抗病毒因子显示为热稳定或热不稳定。在肝素结合部分和非结合部分以及通过反相HPLC分离的部分中鉴定出抑制活性。FIV抑制与I型或II型干扰素无关。α和β趋化因子都不太可能是候选因子,因为分子排阻离心表明主要因子大于50 kD。从猫淋巴细胞产生的可溶性抑制活性特性中确定的定性差异表明,多种因子负责FIV复制的非细胞溶解性CD8 + T细胞抑制。