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Broadly Neutralizing Antibodies and Viral Inducers Decrease Rebound from HIV-1 Latent Reservoirs in Humanized Mice

机译:广泛中和的抗体和病毒诱导剂减少了人源化小鼠HIV-1潜在贮库的反弹。

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摘要

Latent reservoirs of HIV-1-infected cells are refractory to antiretroviral therapies (ART) and remain the major barrier to curing HIV-1. Because latently infected cells are long-lived, immunologically invisible, and may undergo homeostatic proliferation, a ''shock and kill'' approach has been proposed to eradicate this reservoir by combining ART with inducers of viral transcription. However, all attempts to alter the HIV-1 reservoir in vivo have failed to date. Using humanized mice, we show that broadly neutralizing antibodies (bNAbs) can interfere with establishment of a silent reservoir by Fc-FcR-mediated mechanisms. In established infection, bNAbs or bNAbs plus single inducers are ineffective in preventing viral rebound. However, bNAbs plus a combination of inducers that act by independent mechanisms synergize to decrease the reservoir as measured by viral rebound. Thus, combinations of inducers and bNAbs constitute a therapeutic strategy that impacts the establishment and maintenance of the HIV-1 reservoir in humanized mice.
机译:被HIV-1感染的细胞的潜在贮库对抗逆转录病毒疗法(ART)无效,并且仍然是治愈HIV-1的主要障碍。由于潜伏感染的细胞是长寿的,在免疫学上是不可见的,并且可能会经历稳态增殖,因此提出了一种“电击并杀死”的方法,通过将ART与病毒转录诱导剂结合来根除该储库。但是,迄今为止,所有尝试改变体内HIV-1储库的尝试均未成功。使用人源化的小鼠,我们显示广泛中和抗体(bNAbs)可以通过Fc-FcR介导的机制干扰沉默的贮库的建立。在确定的感染中,bNAb或bNAb加单一诱导剂在预防病毒反弹方面无效。但是,bNAbs加上通过独立机制发挥作用的诱导剂组合可协同作用,从而通过病毒反弹来减少储库。因此,诱导剂和bNAb的组合构成了一种治疗策略,会影响人源化小鼠中HIV-1贮库的建立和维持。

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