Eckard Allison Ross, Rosebush Julia C, O'Riordan Mary Ann, Graves Chanda C, Alexander Ashley, Grover Anita K, Lee S Thera, Habib Jakob G, Ruff Joshua H, Chahroudi Ann, McComsey Grace A
Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Department of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Antivir Ther. 2017;22(8):669-680. doi: 10.3851/IMP3157.
HIV-infected individuals are at increased risk of neurocognitive impairment compared to the general population. Studies suggest that, despite combination antiretroviral therapy (cART), HIV infection causes immune activation which results in neural damage; however, few data exist in HIV-infected youth.
HIV-infected youth 8-26-years-old on cART with virological suppression were prospectively enrolled along with healthy controls. Neurocognitive performance was assessed by age-appropriate Wechsler Intelligence Scales. Soluble and cellular markers of T-lymphocyte and monocyte activation were measured by ELISA and flow cytometry, respectively.
45 HIV-infected subjects and 21 controls were enrolled. Markers of T-cell and monocyte activation were higher in the HIV-infected subjects compared to controls, but proportions of inflammatory and patrolling monocytes were similar. Although there were no significant differences in neurocognitive scores between the HIV-infected and control groups, scores were low-average for four of five testing domains for the HIV-infected subjects and average for all five in the controls, and % of HIV-infected subjects with scores classified as 'low average' or below was higher than in the controls. Variables most associated with neurocognitive performance among HIV-infected subjects included activated CD4 T-cells (% CD4+CD38+HLA-DR), monocyte activation (soluble CD14), HIV duration, age and sex.
HIV-infected youth on cART with virological suppression show subtle evidence of neurocognitive impairment compared to healthy controls, and increased immune activation appears to play a role. Additional studies are needed to develop strategic interventions beyond cART to potentially improve neurocognitive performance and/or minimize further impairment in this vulnerable population. ClinicalTrials.gov Identifier: NCT01523496.
与普通人群相比,感染人类免疫缺陷病毒(HIV)的个体发生神经认知障碍的风险更高。研究表明,尽管采用了联合抗逆转录病毒疗法(cART),HIV感染仍会导致免疫激活,进而造成神经损伤;然而,关于感染HIV的青年的数据却很少。
前瞻性纳入8至26岁接受cART且病毒学得到抑制的HIV感染青年以及健康对照者。通过适合年龄的韦氏智力量表评估神经认知表现。分别采用酶联免疫吸附测定(ELISA)和流式细胞术检测T淋巴细胞和单核细胞激活的可溶性及细胞标志物。
共纳入45名HIV感染受试者和21名对照者。与对照组相比,HIV感染受试者的T细胞和单核细胞激活标志物更高,但炎性单核细胞和巡逻单核细胞的比例相似。尽管HIV感染组和对照组之间的神经认知评分无显著差异,但HIV感染受试者在五个测试领域中的四个领域的得分处于低平均水平,而对照组的所有五个领域得分均为平均水平,且HIV感染受试者中得分被归类为“低平均水平”或更低的百分比高于对照组。在HIV感染受试者中,与神经认知表现最相关的变量包括活化的CD4 T细胞(% CD4+CD38+HLA-DR)、单核细胞激活(可溶性CD14)、HIV感染持续时间、年龄和性别。
与健康对照者相比,接受cART且病毒学得到抑制的HIV感染青年表现出神经认知障碍的细微迹象,免疫激活增加似乎起到了一定作用。需要开展更多研究,以制定除cART之外的策略性干预措施,从而有可能改善这一脆弱人群的神经认知表现和/或尽量减少进一步的损害。临床试验.gov标识符:NCT01523496。