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Hepatitis B Virus Vaccination in HIV-1-Infected Young Adults: A Tool to Reduce the Size of HIV-1 Reservoirs?

机译:在感染HIV-1的年轻成年人中进行乙肝病毒疫苗接种:减少HIV-1储库大小的工具?

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摘要

During anti-retroviral therapy (ART) HIV-1 persists in cellular reservoirs, mostly represented by CD4+ memory T cells. Several approaches are currently being undertaken to develop a cure for HIV-1 infection through elimination (or reduction) of these reservoirs. Few studies have so far been conducted to assess the possibility of reducing the size of HIV-1 reservoirs through vaccination in virologically controlled HIV-1-infected children. We recently conducted a vaccination study with a combined hepatitis A virus (HAV) and hepatitis B virus (HBV) vaccine in 22 HIV-1-infected children. We assessed the size of the virus reservoir, measured as total HIV-1 DNA copies in blood cells, pre- and postvaccination. In addition, we investigated by immunostaining whether the frequencies of CD4+ and CD8+ T cells and parameters of immune activation and proliferation on these cells were modulated by vaccination. At 1 month from the last vaccination dose, we found that 20 out of 22 children mounted a serological response to HBV; a majority of children had antibodies against HAV at baseline. The number of HIV-1 DNA copies in blood at 1 month postvaccination was reduced in comparison to baseline although this reduction was not statistically significant. A significant reduction of HIV-1 DNA copies in blood following vaccination was found in 12 children. The frequencies of CD4+ (naïve, effector memory) and CD8+ (central memory) T-cell subpopulations changed following vaccinations and a reduction in the activation and proliferation pattern of these cells was also noticed. Multivariate linear regression analysis revealed that the frequency of CD8+ effector memory T cells prior to vaccination was strongly predictive of the reduction of HIV-1 DNA copies in blood following vaccination of the 22 HIV-1-infected children. The results of this study suggest a beneficial effect of vaccination to reduce the size of virus reservoir in HIV-1-infected children receiving ART. A reduced frequency of activated CD4+ cells and an increase in central memory CD8+ T cells were associated with this finding. Further studies should assess whether vaccination is a possible tool to reduce HIV-1 reservoirs.
机译:在抗逆转录病毒疗法(ART)期间,HIV-1持续存在于细胞储库中,主要表现为CD4 +记忆T细胞。通过消除(或减少)这些水库,目前正在采取几种方法来开发治疗HIV-1感染的方法。迄今为止,很少有研究评估通过病毒控制的感染HIV-1的儿童接种疫苗来减少HIV-1储存库大小的可能性。我们最近对22名感染HIV-1的儿童进行了联合A型肝炎病毒(HAV)和B型肝炎病毒(HBV)疫苗的疫苗接种研究。我们评估了病毒库的大小,以接种前和接种后血细胞中HIV-1 DNA的总拷贝数衡量。此外,我们通过免疫染色研究了CD4 +和CD8 + T细胞的频率以及这些细胞上免疫激活和增殖的参数是否通过疫苗接种来调节。在上次接种疫苗后1个月,我们发现22名儿童中有20名对HBV产生了血清学反应;大多数儿童在基线时都有抗HAV的抗体。与基线相比,疫苗接种后1个月血液中HIV-1 DNA拷贝数减少了,尽管这种减少没有统计学意义。接种疫苗后,有12名儿童的血液中HIV-1 DNA拷贝显着减少。接种疫苗后,CD4 +(幼稚的,效应记忆)和CD8 +(中央记忆)T细胞亚群的频率发生了变化,这些细胞的活化和增殖模式也有所降低。多元线性回归分析显示,接种疫苗之前CD8 +效应记忆T细胞的频率强烈预测了接种22个HIV-1感染儿童后血液中HIV-1 DNA拷贝的减少。这项研究的结果表明,接种疫苗有助于减少接受ART的HIV-1感染儿童的病毒库大小。这一发现与活化的CD4 +细胞的频率降低和中央记忆CD8 + T细胞的增加有关。进一步的研究应评估疫苗接种是否可能是减少HIV-1储存库的工具。

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