Patterson B K, Behbahani H, Kabat W J, Sullivan Y, O'Gorman M R, Landay A, Flener Z, Khan N, Yogev R, Andersson J
Department of Pediatrics, Division of Infectious Diseases, Children's Memorial Hospital/Northwestern University Medical School, 2300 Children's Plaza #51, Chicago, Illinois 60614, USA.
J Clin Invest. 2001 Feb;107(3):287-94. doi: 10.1172/JCI11481.
The placenta may play a critical role in inhibiting vertical transmission of HIV-1. Here we demonstrate that leukemia inhibitory factor (LIF) is a potent endogenous HIV-1-suppressive factor produced locally in placentae. In vitro, LIF exerted a potent, gp130-LIFRbeta-dependent, HIV coreceptor-independent inhibition of HIV-1 replication with IC50 values between 0.1 pg/ml and 0.7 pg/ml, depending on the HIV-1 isolate. LIF also inhibited HIV-1 in placenta and thymus tissues grown in ex vivo organ culture. The level of LIF mRNA and the incidence of LIF protein-expressing cells were significantly greater in placentae from HIV-1-infected women who did not transmit HIV-1 to their fetuses compared with women who transmitted the infection, but they were not significantly different from placentae of uninfected mothers. These findings demonstrate a novel pathway for endogenous HIV suppression that may prove to be an effective immune therapy for HIV infection.
胎盘可能在抑制HIV-1垂直传播中发挥关键作用。在此我们证明,白血病抑制因子(LIF)是胎盘局部产生的一种有效的内源性HIV-1抑制因子。在体外,LIF对HIV-1复制发挥了强大的、gp130-LIFRβ依赖性的、不依赖HIV共受体的抑制作用,IC50值在0.1 pg/ml至0.7 pg/ml之间,具体取决于HIV-1分离株。LIF还抑制了离体器官培养中生长的胎盘和胸腺组织中的HIV-1。与将感染传播给胎儿的女性相比,未将HIV-1传播给胎儿的HIV-1感染女性的胎盘中,LIF mRNA水平和表达LIF蛋白的细胞发生率显著更高,但与未感染母亲的胎盘无显著差异。这些发现证明了一种新的内源性HIV抑制途径,这可能被证明是一种有效的HIV感染免疫疗法。