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Variation in HIV-1 R5 macrophage-tropism correlates with sensitivity to reagents that block envelope: CD4 interactions but not with sensitivity to other entry inhibitors

机译:HIV-1 R5巨噬细胞嗜性的变化与对阻断包膜的试剂的敏感性相关:CD4相互作用但与对其他进入抑制剂的敏感性无关

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摘要

BackgroundHIV-1 R5 viruses cause most of the AIDS cases worldwide and are preferentially transmitted compared to CXCR4-using viruses. Furthermore, R5 viruses vary extensively in capacity to infect macrophages and highly macrophage-tropic variants are frequently identified in the brains of patients with dementia. Here, we investigated the sensitivity of R5 envelopes to a range of inhibitors and antibodies that block HIV entry. We studied a large panel of R5 envelopes, derived by PCR amplification without culture from brain, lymph node, blood and semen. These R5 envelopes conferred a wide range of macrophage tropism and included highly macrophage-tropic variants from brain and non-macrophage-tropic variants from lymph node.
机译:背景HIV-1 R5病毒在全世界引起大多数AIDS病例,与使用CXCR4的病毒相比,其优先传播。此外,R5病毒感染巨噬细胞的能力差异很大,在痴呆症患者的大脑中经常发现高度嗜巨噬细胞的变异。在这里,我们研究了R5包膜对一系列阻断HIV进入的抑制剂和抗体的敏感性。我们研究了一大批R5包膜,这些包膜是通过PCR扩增从大脑,淋巴结,血液和精液中进行培养而得。这些R5包膜赋予了广泛的巨噬细胞嗜性,包括来自大脑的高度巨噬细胞嗜性变异和来自淋巴结的非巨噬细胞嗜性变异。

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