Department of Tropical Medicine, Medical Microbiology & Pharmacology, John A. Burns School of Medicine, University of Hawai'i, 651 Ilalo St BSB 325, Honolulu, HI, 96813, USA.
Hawai'i Center for AIDS, John A. Burns School of Medicine, University of Hawai'i, 651 Ilalo St BSB 225, Honolulu, HI, 96813, USA.
J Neurovirol. 2019 Apr;25(2):150-161. doi: 10.1007/s13365-018-0696-3. Epub 2018 Nov 26.
We previously reported that galectin-9 (Gal-9), a soluble lectin with immunomodulatory properties, is elevated in plasma during HIV infection and induces HIV transcription. The link between Gal-9 and compromised neuronal function is becoming increasingly evident; however, the association with neuroHIV remains unknown. We measured Gal-9 levels by ELISA in cerebrospinal fluid (CSF) and plasma of 70 HIV-infected (HIV+) adults stratified by age (older > 40 years and younger < 40 years) either ART suppressed or with detectable CSF HIV RNA, including a subgroup with cognitive assessments, and 18 HIV uninfected (HIV-) controls. Gal-9 tissue expression was compared in necropsy brain specimens from HIV- and HIV+ donors using gene datasets and immunohistochemistry. Among older HIV+ adults, CSF Gal-9 was elevated in the ART suppressed and CSF viremic groups compared to controls, whereas in the younger group, Gal-9 levels were elevated only in the CSF viremic group (p < 0.05). CSF Gal-9 positively correlated with age in all groups (p < 0.05). CSF Gal-9 tracked with CSF HIV RNA irrespective of age (β = 0.33; p < 0.05). Higher CSF Gal-9 in the older viremic HIV+ group correlated with worse neuropsychological test performance scores independently of age and CSF HIV RNA (p < 0.05). Furthermore, CSF Gal-9 directly correlated with myeloid activation (CSF-soluble CD163 and neopterin) in both HIV+ older groups (p < 0.05). Among HIV+ necropsy specimens, Gal-9 expression was increased in select brain regions compared to controls (p < 0.05). Gal-9 may serve as a novel neuroimmuno-modulatory protein that is involved in driving cognitive deficits in those aging with HIV and may be valuable in tracking cognitive abnormalities.
我们之前报道过,具有免疫调节特性的可溶性凝集素半乳糖凝集素-9(Gal-9)在 HIV 感染期间在血浆中升高,并诱导 HIV 转录。Gal-9 与受损的神经元功能之间的联系越来越明显;然而,与神经 HIV 的关联尚不清楚。我们通过酶联免疫吸附试验(ELISA)测量了 70 名 HIV 感染(HIV+)成年人的脑脊液(CSF)和血浆中的 Gal-9 水平,这些成年人根据年龄(大于 40 岁和小于 40 岁)分层,分为接受抗逆转录病毒治疗(ART)且 CSF 中 HIV RNA 不可检测或有检测到的,包括进行认知评估的亚组,以及 18 名未感染 HIV(HIV-)的对照者。我们使用基因数据集和免疫组织化学比较了尸检脑组织中 HIV-和 HIV+供体的 Gal-9 组织表达。在年龄较大的 HIV+成年人中,与对照组相比,ART 抑制组和 CSF 病毒血症组的 CSF Gal-9 升高,而在年龄较小的组中,仅在 CSF 病毒血症组中 Gal-9 水平升高(p<0.05)。所有组的 CSF Gal-9 均与年龄呈正相关(p<0.05)。无论年龄大小,CSF Gal-9 与 CSF HIV RNA 相关(β=0.33;p<0.05)。年龄较大的病毒血症 HIV+组中较高的 CSF Gal-9 与神经心理学测试表现评分的下降相关,与年龄和 CSF HIV RNA 无关(p<0.05)。此外,CSF Gal-9 与两种 HIV+老年组中的髓样细胞激活(CSF 可溶性 CD163 和新蝶呤)直接相关(p<0.05)。在 HIV+尸检标本中,与对照组相比,Gal-9 在某些脑区的表达增加(p<0.05)。Gal-9 可能是一种新型的神经免疫调节蛋白,参与驱动 HIV 感染者的认知缺陷,可能对跟踪认知异常有价值。