首页> 外文期刊>MBio >Simian Immunodeficiency Virus-Infected Memory CD4 + T Cells Infiltrate to the Site of Infected Macrophages in the Neuroparenchyma of a Chronic Macaque Model of Neurological Complications of AIDS
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Simian Immunodeficiency Virus-Infected Memory CD4 + T Cells Infiltrate to the Site of Infected Macrophages in the Neuroparenchyma of a Chronic Macaque Model of Neurological Complications of AIDS

机译:Simian免疫缺陷病毒感染的记忆CD4 + T细胞渗透到感染的巨噬细胞位点,在疗养的神经和疗法慢性猕猴的神经外科模型

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Simian immunodeficiency virus (SIV)-infected nonhuman primates can serve as a relevant model for AIDS neuropathogenesis. Current SIV-induced encephalitis (SIVE)/neurological complications of AIDS (neuroAIDS) models are generally associated with rapid progression to neuroAIDS, which does not reflect the tempo of neuroAIDS progression in humans. Recently, we isolated a neuropathogenic clone, SIVsm804E-CL757 (CL757), obtained from an SIV-infected rhesus macaque (RM). CL757 causes a more protracted progression to disease, inducing SIVE in 50% of inoculated animals, with high cerebral spinal fluid viral loads, multinucleated giant cells (MNGCs), and perivascular lymphocytic cuffing in the central nervous system (CNS). This latter finding is reminiscent of human immunodeficiency virus (HIV) encephalitis in humans but not generally observed in rapid progressor animals with neuroAIDS. Here, we studied which subsets of cells within the CNS were targeted by CL757 in animals with neurological symptoms of SIVE. Immunohistochemistry of brain sections demonstrated infiltration of CD4 ~(+) T cells (CD4) and macrophages (MΦs) to the site of MNGCs. Moreover, an increase in mononuclear cells isolated from the brain tissues of RMs with SIVE correlated with increased cerebrospinal fluid (CSF) viral load. Subset analysis showed a specific increase in brain CD4 ~(+) memory T cells (Br-mCD4), brain-MΦs (Br-MΦs), and brain B cells (Br-B cells). Both Br-mCD4s and Br-MΦs harbored replication-competent viral DNA, as demonstrated by virus isolation by coculture. However, only in animals exhibiting SIVE/neuroAIDS was virus isolated from Br-MΦs. These findings support the use of CL757 to study the pathogenesis of AIDS viruses in the central nervous system and indicate a previously unanticipated role of CD4s cells as a potential reservoir in the brain.
机译:Simian免疫缺陷病毒(SIV) - 摄入的非人的灵长类动物可以作为艾滋病神经病理学的相关模型。目前的SIV诱导的脑炎(艾滋病)/艾滋病(神经职业)模型的神经系统并发症通常与神经外德的快速进展相关,这不会反映人类神经外德进展的节奏。最近,我们分离出一种神经疗法克隆SIVSM804E-CL757(CL757),得到了由SIV感染的恒河猴(RM)获得的。 CL757对疾病产生更长的进展,诱导50%的接种动物,具有高脑脊髓液病毒载,多核巨细胞(MNGC)和中枢神经系统(CNS)中的血管淋巴细胞肿胀。后一种发现是让人类免疫缺陷病毒(HIV)脑炎中的一种,但通常在具有神经外的快速进化动物中观察到。在这里,我们研究了CNS内的哪些细胞亚群由CL757在动物中的患者的神经系统症状靶向。脑切片的免疫组织化学证明了CD4〜(+)T细胞(CD4)和巨噬细胞(Mφs)的浸润到MNGCs的部位。此外,具有与增加的脑脊液(CSF)病毒载量相关的RMS脑组织中分离的单核细胞的增加。子集分析显示脑CD4〜(+)内存T细胞(BR-MCD4),脑-MφS(BR-MφS)和脑B细胞(BR-B细胞)的特异性增加。 BR-MCD4S和BR-MφS都覆盖着竞争态病毒DNA,如通过共培养的病毒分离所证明的。然而,只有在表现出Sive /神经外的动物是从BR-MφS中分离的病毒。这些发现支持CL757研究中枢神经系统中艾滋病病毒的发病机制,并表明CD4S细胞作为大脑中潜在储层的先前意外的作用。

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