...
首页> 外文期刊>Clinical & developmental immunology. >Role of In Vitro Stimulation with Lipopolysaccharide on T-Cell Activation in HIV-Infected Antiretroviral-Treated Patients
【24h】

Role of In Vitro Stimulation with Lipopolysaccharide on T-Cell Activation in HIV-Infected Antiretroviral-Treated Patients

机译:脂多糖体外刺激对HIV感染的抗逆转录病毒治疗患者T细胞活化的作用

获取原文

摘要

We investigated the effect of LPS in vitro stimulation on T-cell activation in HIV-infected patients with different CD4+ recovery on HAART. PBMCs from 30 HIV-positive, HAART-treated, aviremic individuals with different CD4+ reconstitution (Low Responders: CD4+ < 350/ μ L; Intermediate Responders: CD4+ 350–599/ μ L; High Responders: CD4+ ≥ 600/ μ L) were cultured with LPS and the proportion of HLA-DR/CD38- and Ki67-expressing CD4+/CD8+ T-cells was measured (flow cytometry). Upon LPS stimulation, significantly higher CD4+ and CD8+HLA-DR+ cells were shown in LR and IR versus HIV-negative controls. While no differences in the proportion of LPS-stimulated CD4+CD38+ cells were recorded amongst HIV-positive subgroups, CD8+CD38+ cells were more elevated in patients with lower CD4+ recovery on HAART (i.e., LR and IR). Upon in vitro LPS stimulation, HLA-DR and CD38 expression on T-cells are differentially regulated. While HLA-DR induction reflects impaired CD4+ reconstitution on HAART, cell-surface CD38 expression is increased only on CD8+ T-cells, allowing to speculate that the sole induction of CD38 on CD4+ cells may not be sufficient to depict LPS-driven immune activation in HIV.
机译:我们调查了LPS体外刺激对HIV感染患者HAART上具有不同CD4 +恢复的T细胞活化的影响。来自30名具有不同CD4 +重构的经HIV阳性,HAART治疗的航空个体的PBMC(低应答者:CD4 + <350 /μL;中应答者:CD4 + 350-599 /μL;高应答者:CD4 +≥600 /μL)用LPS培养,并测量表达HLA-DR / CD38-和Ki67的CD4 + / CD8 + T细胞的比例(流式细胞仪)。 LPS刺激后,LR和IR中的CD4 +和CD8 + HLA-DR +细胞明显高于HIV阴性对照。虽然在HIV阳性亚组中没有发现LPS刺激的CD4 + CD38 +细胞比例的差异,但是在HAART上CD4 +回收率较低的患者(即LR和IR)中,CD8 + CD38 +细胞的含量更高。在体外LPS刺激后,T细胞上的HLA-DR和CD38表达受到差异调节。虽然HLA-DR诱导反映了HAART上CD4 +重构受损,但细胞表面CD38表达仅在CD8 + T细胞上增加,这可以推测CD4 +细胞上CD38的唯一诱导可能不足以描述LPS驱动的免疫激活。艾滋病病毒。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号