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首页> 外文期刊>Frontiers in Immunology >Hepatitis B Virus Vaccination in HIV-1-Infected Young Adults: A Tool to Reduce the Size of HIV-1 Reservoirs?
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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:乙型肝炎病毒疫苗接种在HIV-1感染的年轻人中:一种减少HIV-1水库大小的工具?

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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+ (na?ve, 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(第ART)期间HIV-1在细胞储存器中持续存在,主要由CD4 +记忆T细胞表示。目前正在采用几种方法来通过消除(或减少)这些水库来制定治愈HIV-1感染。到目前为止,迄今为止已经进行了很少的研究,以评估通过在病毒学控制的HIV-1感染儿童中的疫苗接种来降低HIV-1储层大小的可能性。我们最近在22名HIV-1感染儿童中患上了一种疫苗接种研究,甲型肝炎病毒(HAV)和乙型肝炎病毒(HBV)疫苗。我们评估了病毒储层的大小,以血细胞的总HIV-1 DNA副本测量,预先和后检测。此外,通过免疫染色CD4 +和CD8 + T细胞和这些细胞上的免疫活化和增殖参数的频率来研究。在最后一次疫苗接种剂量的1个月,我们发现22名儿童中的20个血液响应HBV;大多数孩子患有基线的抗体。与基线相比,1个月后血液中HIV-1 DNA拷贝的拷贝数减少,尽管这种减少没有统计学意义。在12名儿童中发现了疫苗接种后的HIV-1 DNA拷贝的显着降低。还注意到,CD4 +(Naαve,效应存储器)和CD8 +(中央记忆)T细胞亚族的频率也在接种疫苗接种后改变,并且还注意到这些细胞的活化和增殖模式的降低。多变量线性回归分析显示,在接种22例HIV-1感染的儿童接种后,疫苗接种前的CD8 +效应记忆记忆T细胞的频率强烈预测到血液中的HIV-1 DNA拷贝的减少。本研究的结果表明,疫苗接种以减少接受艺术的HIV-1感染儿童病毒储层大小的有益效果。活化CD4 +细胞的降低频率和中央记忆CD8 + T细胞的增加与该发现有关。进一步的研究应评估疫苗接种是减少HIV-1水库的可能工具。

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