首页> 外文期刊>Virology >RANTES, IFN- gamma , CCR1, and CCR5 mRNA Expression in Peripheral Blood, Lymph Node, and Bronchoalveolar Lavage Mononuclear Cells during Primary Simian Immunodeficiency Virus Infection of Macaques
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RANTES, IFN- gamma , CCR1, and CCR5 mRNA Expression in Peripheral Blood, Lymph Node, and Bronchoalveolar Lavage Mononuclear Cells during Primary Simian Immunodeficiency Virus Infection of Macaques

机译:猕猴免疫原性病毒感染猕猴期间外周血,淋巴结和支气管肺泡灌洗单核细胞中RANTES,IFN-γ,CCR1和CCR5 mRNA表达

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Primary infection of macaques with pathogenic isolates of simian immunodeficiency virus (SIV) (as a model of HIV infection in humans) represents a unique opportunity to study early lentivirus /host interactions. We sought to determine whether there is a temporal relationship linking SIV replication and dissemination and the expression of the chemokine RANTES (regulated upon activation normal T cell expressed and secreted) and the SIV/HIV coreceptor CCR5 in different tissues during acute SIV infection of macaques. Four cynomolgus macaques were inoculated intravenously with a pathogenic primary isolate of SIVmac251. RT-PCR was used to monitor the expression of RANTES and CCR5 mRNA in fresh isolated mononuclear cells from blood, lymph node, and bronchoalveolar lavages. These expressions were compared to those of IFN- gamma as an indicator of the development of the immune response and to another receptor for RANTES, CCR1, which is not described as a coreceptor for SIV/HIV-1 entry. An enhancement of CCR1/CCR5 mRNA expression was noticed during primary SIVmac251 infection of macaques, mainly in tissue. In the three different compartments investigated, IFN- gamma and RANTES overexpression was noticed by the time of systemic viral replication containment. Our results put CCR5 and RANTES mRNA expression back in the context of inflammatory and immune responses to SIV primary infection.
机译:用猿猴免疫缺陷病毒(SIV)(作为人类HIV感染的模型)的病原分离株对猕猴进行的初次感染代表了研究早期慢病毒/宿主相互作用的独特机会。我们试图确定在猕猴急性SIV感染期间不同组织中SIV复制和传播与趋化因子RANTES(受激活的正常T细胞表达和分泌的调节)和SIV / HIV核心受体CCR5的表达之间是否存在时间关系。用病原体SIVmac251静脉内接种四只食蟹猕猴。 RT-PCR用于监测血液,淋巴结和支气管肺泡灌洗液中新鲜分离的单个核细胞中RANTES和CCR5 mRNA的表达。将这些表达与作为免疫应答发展指标的IFN-γ以及与RANTES的另一种受体CCR1(未描述为SIV / HIV-1进入的共受体)进行了比较。在猕猴原发性SIVmac251感染期间(主要在组织中)注意到CCR1 / CCR5 mRNA表达增强。在研究的三个不同的区室中,系统性病毒复制抑制的时间注意到了IFN-γ和RANTES的过表达。我们的结果将CCR5和RANTES mRNA表达恢复到对SIV原发感染的炎症和免疫反应中。

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