Hawaii Center for AIDS, John A. Burns School of Medicine, University of Hawai'i at Manoa, Honolulu, HI, 96813, USA.
Department of Tropical Medicine, Medical Microbiology, and Pharmacology, John A. Burns School Medicine, University of Hawai'i at Manoa, Honolulu, HI, 96813, USA.
Sci Rep. 2023 Aug 16;13(1):13282. doi: 10.1038/s41598-023-40475-0.
While the protective role of neutrophil extracellular traps (NETs) in limiting human immunodeficiency virus (HIV) spread to susceptible cells has been documented, there is comparatively little insight into whether NET formation is harmful in people living with HIV (PLWH). To gain insight into neutrophil dysregulation and the pathological role of NETs in HIV, we examined expressions of NET-associated markers [cell-free DNA (cfDNA) and citrullinated histone H3 (CitH3)] in the plasmas from a cohort of the Hawaii Aging with HIV-cardiovascular and HIV-seronegative (HIV-) individuals. In a subset of participants, circulating low-density granulocyte (LDG) levels and their maturation and activation status were analyzed via flow cytometry. We demonstrated higher plasma levels of CitH3 in PLWH compared to HIV- individuals. LDGs from PLWH had heightened CD66b, but reduced CD16 expression. The percentages and counts of CD10 LDGs were significantly decreased in PLWH. In addition, the CD16 LDG subsets were enriched in PLWH, compared to HIV- group, indicating that immature LDGs are increased in PLWH. Moreover, LDGs from PLWH exhibited significantly higher NET forming capacity. In summary, our study presents evidence that LDGs from PLWH on ART display an immature and altered phenotype with increased NET formation. Among PLWH, plasma NET levels as well as LDG parameters correlated with blood markers for inflammation and coagulation, suggesting that neutrophil activation and NETs may exert proinflammatory and coagulation effects. Our data provide insights into the pathologic role of LDGs at least in part mediated through NET formation in PLWH.
虽然已经有文献证明中性粒细胞细胞外陷阱(NETs)在限制人类免疫缺陷病毒(HIV)传播到易感细胞方面具有保护作用,但对于 HIV 感染者(PLWH)中 NET 形成是否有害,人们的了解相对较少。为了深入了解中性粒细胞失调以及 NET 在 HIV 中的病理作用,我们检测了来自夏威夷艾滋病毒-心血管和 HIV-个体队列的血浆中与 NET 相关的标志物[无细胞 DNA(cfDNA)和瓜氨酸化组蛋白 H3(CitH3)]的表达。在一部分参与者中,通过流式细胞术分析了循环低密粒细胞(LDG)的水平及其成熟和激活状态。我们发现,与 HIV-个体相比,PLWH 的血浆 CitH3 水平更高。PLWH 的 LDG 表达更高的 CD66b,但 CD16 表达降低。PLWH 的 CD10 LDG 百分比和计数显著减少。此外,与 HIV-组相比,PLWH 中的 CD16 LDG 亚群明显增加,表明不成熟的 LDG 在 PLWH 中增加。此外,与 HIV-组相比,PLWH 的 LDG 亚群表达更高的 NET 形成能力。总之,我们的研究提供了证据表明,接受 ART 的 PLWH 的 LDG 表现出不成熟和改变的表型,并且 NET 形成增加。在 PLWH 中,血浆 NET 水平以及 LDG 参数与炎症和凝血的血液标志物相关,这表明中性粒细胞激活和 NET 可能发挥促炎和凝血作用。我们的数据至少部分揭示了 LDG 通过 NET 形成在 PLWH 中的病理作用。