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Short Communication: Activating Stimuli Enhance Immunotoxin-Mediated Killing of HIV-Infected Macrophages

机译:简短交流:激活刺激物增强免疫毒素介导的HIV感染巨噬细胞的杀伤。

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摘要

Strategies for purging persistent reservoirs in human immunodeficiency virus (HIV)-infected individuals may be enhanced by including agents that specifically kill virus-expressing cells. Anti-HIV envelope immunotoxins (ITs) represent one class of candidate molecules that could fulfill this function. We have previously utilized an anti-gp120 IT in conjunction with various stimulants to kill latently infected T cells ex vivo. Here we show that primary macrophages expressing HIV Env are relatively refractory to killing by IT when used alone. However, including stimulants such as prostratin or granulocyte–macrophage colony-stimulating factor to increase HIV gene expression in infected macrophages enhanced IT-mediated killing. Therefore, “activation–elimination” strategies similar to those proposed for purging the latent HIV reservoir may prove useful in clearing chronically infected macrophages in vivo
机译:可以通过包括特异性杀死表达病毒的细胞的药物来增强清除感染人类免疫缺陷病毒(HIV)的个体中持久性储库的策略。抗HIV包膜免疫毒素(IT)代表了一类可以实现此功能的候选分子。我们先前已将抗gp120 IT与各种刺激剂结合使用,以离体杀死潜伏感染的T细胞。在这里,我们表明表达HIV Env的原代巨噬细胞单独使用时相对较难被IT杀死。但是,包括刺激素,例如前列蛋白或粒细胞-巨噬细胞集落刺激因子,以增加感染的巨噬细胞中的HIV基因表达,增强了IT介导的杀伤力。因此,类似于提议的清除潜在HIV病毒库的“活化-消除”策略可能对体内清除慢性感染的巨噬细胞有用。

著录项

  • 来源
    《AIDS Research and Human Retroviruses》 |2008年第11期|p.1399-1404|共6页
  • 作者单位

    Department of Medicine, Division of Hematology and Oncology, David Geffen School of Medicine at UCLA, Los Angeles, California 90095.UCLA AIDS Institute, David Geffen School of Medicine at UCLA, Los Angeles, California 90095.;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    HIV; IT;

    机译:艾滋病毒;

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