Department of Molecular Biology, Immunology and Pathology, College of Veterinary Medicine and Biological Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Sprague Medical and Scientific Communications, LLC, Fort Collins, CO 80528, USA.
Viruses. 2018 Apr 20;10(4):210. doi: 10.3390/v10040210.
We previously showed that cats that were infected with non-pathogenic Puma lentivirus (PLV) and then infected with pathogenic feline immunodeficiency virus (FIV) (co-infection with the host adapted/pathogenic virus) had delayed FIV proviral and RNA viral loads in blood, with viral set-points that were lower than cats infected solely with FIV. This difference was associated with global CD4⁺ T cell preservation, greater interferon gamma (IFN-γ) mRNA expression, and no cytotoxic T lymphocyte responses in co-infected cats relative to cats with a single FIV infection. In this study, we reinforced previous observations that prior exposure to an apathogenic lentivirus infection can diminish the effects of acute infection with a second, more virulent, viral exposure. In addition, we investigated whether the viral load differences that were observed between PLV/FIV and FIV infected cats were associated with different immunocyte phenotypes and cytokines. We found that the immune landscape at the time of FIV infection influences the infection outcome. The novel findings in this study advance our knowledge about early immune correlates and documents an immune state that is associated with PLV/FIV co-infection that has positive outcomes for lentiviral diseases.
我们之前的研究表明,感染了非致病性美洲狮慢病毒(PLV),随后又感染了致病性猫免疫缺陷病毒(FIV)的猫(与宿主适应/致病性病毒的合并感染),其血液中的 FIV 前病毒和 RNA 病毒载量延迟,病毒临界点低于单独感染 FIV 的猫。这种差异与全球 CD4+T 细胞保存、更高的干扰素 γ(IFN-γ)mRNA 表达以及合并感染猫中无细胞毒性 T 淋巴细胞反应有关,而在单一 FIV 感染的猫中则没有这些反应。在这项研究中,我们证实了先前的观察结果,即先前暴露于非致病性慢病毒感染可以减轻第二次更具毒性的病毒急性感染的影响。此外,我们还研究了在 PLV/FIV 和 FIV 感染猫之间观察到的病毒载量差异是否与不同的免疫细胞表型和细胞因子有关。我们发现,FIV 感染时的免疫景观会影响感染结果。本研究的新发现增进了我们对早期免疫相关性的认识,并记录了与 PLV/FIV 合并感染相关的免疫状态,这种状态对慢病毒病有积极影响。