Hohdatsu T, Miyagawa N, Ohkubo M, Kida K, Koyama H
Department of Veterinary Infectious Diseases, School of Veterinary Medicine and Animal Sciences, Kitasato University, Aomori, Japan.
Arch Virol. 2000;145(12):2525-38. doi: 10.1007/s007050070006.
CD8+ T cells in FIV-infected cats inhibit feline immunodeficiency virus (FIV) replication by producing a soluble factor(s). In the present study, four SPF cats were experimentally infected with FIV. The period during which the anti-FIV activity of CD8+ T cells became detectable was investigated, and the presence or absence of this activity in the lymph nodes and spleen was examined. Furthermore, we investigated which step(s) of the FIV replication cycle are affected by this antiviral activity. This antiviral activity became detectable five weeks after FIV infection in early cases, and it was simultaneous with or one week after the induction of humoral immunity. All cats having CD8+ T cells with anti-FIV activity in the peripheral blood also possessed CD8+ T cells with anti-FIV activity in the lymph nodes. In contrast, CD8+ T cells from the spleens of some, but not all cats showed anti-FIV activity. CD8+ T cell-depleted peripheral blood mononuclear cells were cultured and reconstituted with CD8+ T cells on day 12 of culture after confirming FIV replication. The number of FIV proviral DNA copies in the cells did not change, but the amount of FIV p24 antigen production in the culture supernatant and the number of FIV mRNA copies in the cells decreased. These findings suggested that CD8+ T cell anti-FIV activity acts at the level of FIV mRNA synthesis from the FIV proviral DNA, inhibiting FIV replication by a non-cytolytic mechanism.
感染猫免疫缺陷病毒(FIV)的猫体内的CD8 + T细胞通过产生一种或多种可溶性因子来抑制猫免疫缺陷病毒(FIV)的复制。在本研究中,四只无特定病原体(SPF)猫被实验性感染FIV。研究了CD8 + T细胞抗FIV活性可检测到的时期,并检查了淋巴结和脾脏中这种活性的有无。此外,我们研究了FIV复制周期的哪些步骤受这种抗病毒活性影响。在早期病例中,FIV感染后五周可检测到这种抗病毒活性,且与体液免疫诱导同时或在其一周后出现。所有外周血中具有抗FIV活性的CD8 + T细胞的猫,其淋巴结中也具有抗FIV活性的CD8 + T细胞。相比之下,部分(但并非所有)猫脾脏中的CD8 + T细胞显示出抗FIV活性。在确认FIV复制后,于培养第12天对去除CD8 + T细胞的外周血单个核细胞进行培养并用CD8 + T细胞进行重建。细胞中FIV前病毒DNA拷贝数未改变,但培养上清液中FIV p24抗原产生量及细胞中FIV mRNA拷贝数减少。这些发现表明,CD8 + T细胞抗FIV活性作用于FIV前病毒DNA转录FIV mRNA的水平,通过非细胞溶解机制抑制FIV复制。