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自然杀伤细胞中激活型杀伤细胞免疫球蛋白样受体拷贝数变异与恒河猴体内 SIV 复制的控制有关。

Association of activating KIR copy number variation of NK cells with containment of SIV replication in rhesus monkeys.

机构信息

Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States of America.

出版信息

PLoS Pathog. 2011 Dec;7(12):e1002436. doi: 10.1371/journal.ppat.1002436. Epub 2011 Dec 15.

Abstract

While the contribution of CD8⁺ cytotoxic T lymphocytes to early containment of HIV-1 spread is well established, a role for NK cells in controlling HIV-1 replication during primary infection has been uncertain. The highly polymorphic family of KIR molecules expressed on NK cells can inhibit or activate these effector cells and might therefore modulate their activity against HIV-1-infected cells. In the present study, we investigated copy number variation in KIR3DH loci encoding the only activating KIR receptor family in rhesus monkeys and its effect on simian immunodeficiency virus (SIV) replication during primary infection in rhesus monkeys. We observed an association between copy numbers of KIR3DH genes and control of SIV replication in Mamu-A*01⁻ rhesus monkeys that express restrictive TRIM5 alleles. These findings provide further evidence for an association between NK cells and the early containment of SIV replication, and underscore the potential importance of activating KIRs in stimulating NK cell responses to control SIV spread.

摘要

虽然 CD8+细胞毒性 T 淋巴细胞对 HIV-1 传播的早期控制作用已得到充分证实,但 NK 细胞在原发性感染期间控制 HIV-1 复制的作用尚不确定。NK 细胞上表达的高度多态性 KIR 分子家族可以抑制或激活这些效应细胞,因此可能调节它们对 HIV-1 感染细胞的活性。在本研究中,我们研究了编码唯一激活 KIR 受体家族的 KIR3DH 基因座在恒河猴中的拷贝数变异及其对恒河猴原发性感染中猴免疫缺陷病毒(SIV)复制的影响。我们观察到 KIR3DH 基因的拷贝数与表达限制性 TRIM5 等位基因的 Mamu-A*01-恒河猴中 SIV 复制的控制之间存在关联。这些发现为 NK 细胞与 SIV 复制的早期控制之间的关联提供了进一步的证据,并强调了激活的 KIR 在刺激 NK 细胞反应以控制 SIV 传播方面的潜在重要性。

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