首页> 美国卫生研究院文献>other >Antibodies and Antibody Derivatives: New Partners in HIV Eradication Strategies
【2h】

Antibodies and Antibody Derivatives: New Partners in HIV Eradication Strategies

机译:抗体和抗体衍生物:HIV消除策略的新伙伴

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Promptly after primoinfection, HIV generates a pool of infected cells carrying transcriptionally silent integrated proviral DNA, the HIV-1 reservoir. These cells are not cleared by combined antiretroviral therapy (cART), and persist lifelong in treated HIV-infected individuals. Defining clinical strategies to eradicate the HIV reservoir and cure HIV-infected individuals is a major research field that requires a deep understanding of the mechanisms of seeding, maintenance and destruction of latently infected cells. Although CTL responses have been classically associated with the control of HIV replication, and hence with the size of HIV reservoir, broadly neutralizing antibodies (bNAbs) have emerged as new players in HIV cure strategies. Several reasons support this potential role: (i) over the last years a number of bNAbs with high potency and ability to cope with the extreme variability of HIV have been identified; (ii) antibodies not only block HIV replication but mediate effector functions that may contribute to the removal of infected cells and to boost immune responses against HIV; (iii) a series of new technologies have allowed for the in vitro design of improved antibodies with increased antiviral and effector functions. Recent studies in non-human primate models and in HIV-infected individuals have shown that treatment with recombinant bNAbs isolated from HIV-infected individuals is safe and may have a beneficial effect both on the seeding of the HIV reservoir and on the inhibition of HIV replication. These promising data and the development of antibody technology have paved the way for treating HIV infection with engineered monoclonal antibodies with high potency of neutralization, wide coverage of HIV diversity, extended plasma half-life in vivo and improved effector functions. The exciting effects of these newly designed antibodies in vivo, either alone or in combination with other cure strategies (latency reversing agents or therapeutic vaccines), open a new hope in HIV eradication.
机译:初次感染后,HIV会迅速产生一组感染的细胞,这些细胞携带转录沉默的整合前病毒DNA(HIV-1库)。这些细胞无法通过联合抗逆转录病毒疗法(cART)清除,并在经过治疗的HIV感染者体内终身存活。定义根除艾滋病毒库和治愈艾滋病毒感染者的临床策略是一个主要的研究领域,需要深入了解潜伏感染细胞的播种,维持和破坏机制。尽管CTL反应经典地与控制HIV复制有关,因此与HIV储存库的大小有关,但广泛中和抗体(bNAb)已成为HIV治疗策略中的新角色。支持这一潜在作用的原因有几个:(i)在过去几年中,已经发现了许多具有高效力和能力应对艾滋病毒极端变异性的bNAb; (ii)抗体不仅阻断HIV复制,而且介导效应子功能,可能有助于去除感染的细胞并增强针对HIV的免疫反应; (iii)一系列新技术可以用于体外设计具有增强的抗病毒和效应功能的改良抗体。在非人类灵长类动物模型和HIV感染者中的最新研究表明,用分离自HIV感染者的重组bNAb进行治疗是安全的,并且可能对HIV储存库的接种和对HIV复制的抑制均具有有益的作用。 。这些有希望的数据和抗体技术的发展为工程化的单克隆抗体治疗HIV感染铺平了道路,该单克隆抗体具有中和力强,HIV多样性广泛,体内血浆半衰期延长和效应子功能改善的特点。这些新设计的抗体在体内的令人兴奋的效果,无论是单独使用还是与其他治愈策略(潜伏期逆转剂或治疗性疫苗)结合使用,都为根除HIV开辟了新希望。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号