AIDS Immunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, Ctra. Majadahonda-Pozuelo km2, 28220, Madrid, Spain.
Division of Microbiology and Immunology, Department of Pathology, University of Utah School of Medicine, Salt Lake City, UT, 84132, USA.
Curr HIV/AIDS Rep. 2019 Oct;16(5):414-422. doi: 10.1007/s11904-019-00462-5.
HIV-1 infection is incurable due to the existence of latent reservoirs that persist in the face of cART. In this review, we describe the existence of multiple HIV-1 reservoirs, the mechanisms that support their persistence, and the potential use of tyrosine kinase inhibitors (TKIs) to block several pathogenic processes secondary to HIV-1 infection.
Dasatinib interferes in vitro with HIV-1 persistence by two independent mechanisms. First, dasatinib blocks infection and potential expansion of the latent reservoir by interfering with the inactivating phosphorylation of SAMHD1. Secondly, dasatinib inhibits the homeostatic proliferation induced by γc-cytokines. Since homeostatic proliferation is thought to be the main mechanism behind the maintenance of the latent reservoir, we propose that blocking this process will gradually reduce the size of the reservoir. TKIs together with cART will interfere with HIV-1 latent reservoir persistence, favoring the prospect for viral eradication.
由于潜伏储库的存在,HIV-1 感染是无法治愈的,而潜伏储库在 cART 治疗下仍然存在。在这篇综述中,我们描述了 HIV-1 储库的多种存在形式、支持其持续存在的机制,以及使用酪氨酸激酶抑制剂(TKI)来阻断 HIV-1 感染后多种致病过程的潜在用途。
达沙替尼通过两种独立的机制在体外干扰 HIV-1 的持续存在。首先,达沙替尼通过干扰 SAMHD1 的失活磷酸化来阻断感染和潜伏储库的潜在扩增。其次,达沙替尼抑制由 γc-细胞因子诱导的稳态增殖。由于稳态增殖被认为是维持潜伏储库的主要机制,我们提出阻断这一过程将逐渐减少储库的大小。TKI 联合 cART 将干扰 HIV-1 潜伏储库的持续存在,有利于病毒的清除。