Suppr超能文献

南非HIV精英控制者的先天性免疫功能障碍与持续激活

Innate immune dysfunction and persistent activation in South African HIV elite controllers.

作者信息

Mohamed Asisipo, Zungu Yenzekile, Shalekoff Sharon, Ebrahim Osman, Waja Ziyaad, Martinson Neil, Tiemessen Caroline T, Thobakgale Christina

机构信息

School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Centre for HIV and STIs, National Institute for Communicable Diseases, Division of the National Health Laboratory Service, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Front Immunol. 2025 Aug 27;16:1603436. doi: 10.3389/fimmu.2025.1603436. eCollection 2025.

Abstract

BACKGROUND

Elite controllers can spontaneously control HIV-1 infection without antiretroviral treatment but remain at risk of developing non-AIDS-related conditions. The adaptive immune system is key in mediating spontaneous viral control; however, the innate immune response remains understudied. We assessed the quality of the innate immune responses by evaluating the phenotype and function of antigen-presenting cells (APCs) in South African adults living with HIV (PWH).

METHODOLOGY

A total of 73 black South Africans were included in this study. Of these, 55 were living with HIV and included 16 individuals with spontaneous viral control (PWH), 20 HIV progressors (PWH), and 19 individuals suppressed on ART (PWH). Eighteen individuals without HIV infection (PWOH) served as the control group. Monocyte subsets, T cell and monocyte activation and the production of tumour necrosis factor-alpha (TNF-α), interferon-alpha (IFN-α), and interleukin-1 beta (IL-1β) by monocytes, myeloid (mDCs) and plasmacytoid (pDCs) dendritic cells were analyzed using multicolour flow cytometry following stimulation with toll-like receptor (TLR)4 (LPS), TLR7/8 (CL097), and TLR9 (CpG-ODN2216) ligands. Plasma biomarkers, soluble CD14 (sCD14), and D-dimer were assessed using enzyme-linked immunosorbent assay.

RESULTS

Our findings show a reduced expression of CD86 on monocytes of PWH (p=0.04) compared to PWOH. A reduced frequency of the classical monocyte (CD14+CD16) subset in PWH (p=0.02) and PWH (p=0.05) compared to PWOH. TNF-α and IL-1β production was lower in monocytes and mDCs of PWH compared to PWOH post-stimulation with TLR4, and TLR7/8 (all p<0.05). Increased sCD14 levels in PWH compared to PWOH (p=0.01) indicate persistent immune activation, whereas increased D-dimer levels in PWH compared to PWH (p=0.01) and PWH (p=0.04) suggest higher inflammation in PWH.

CONCLUSION

PWH exhibits similar immune responses as other PWH including PWH, their innate immune profiles are characterized by lower levels of monocyte activation, reduced levels of classical monocytes, reduced capacity to produce pro-inflammatory cytokines, and elevated biomarkers associated with unfavourable disease outcomes. These findings highlight the need for continuous monitoring and potential therapeutic interventions to mitigate chronic inflammation in PWH. Furthermore, it expands our understanding of complex innate immune cell responses in PWH.

摘要

背景

精英控制者可在不接受抗逆转录病毒治疗的情况下自发控制HIV-1感染,但仍有发生非艾滋病相关疾病的风险。适应性免疫系统在介导自发病毒控制中起关键作用;然而,固有免疫反应仍研究不足。我们通过评估南非成年HIV感染者(PWH)中抗原呈递细胞(APC)的表型和功能,来评估固有免疫反应的质量。

方法

本研究共纳入73名南非黑人。其中,55名是HIV感染者,包括16名自发病毒控制者(PWH)、20名HIV进展者(PWH)和19名接受抗逆转录病毒治疗后病毒得到抑制的个体(PWH)。18名未感染HIV的个体(PWOH)作为对照组。使用多色流式细胞术分析单核细胞亚群、T细胞和单核细胞活化情况,以及单核细胞、髓样树突状细胞(mDCs)和浆细胞样树突状细胞(pDCs)在受到Toll样受体(TLR)4(LPS)、TLR7/8(CL097)和TLR9(CpG-ODN2216)配体刺激后肿瘤坏死因子-α(TNF-α)、干扰素-α(IFN-α)和白细胞介素-1β(IL-1β)的产生情况。使用酶联免疫吸附测定法评估血浆生物标志物、可溶性CD14(sCD14)和D-二聚体。

结果

我们的研究结果显示,与PWOH相比,PWH的单核细胞上CD86表达降低(p = 0.04)。与PWOH相比,PWH(p = 0.02)和PWH(p = 0.05)中经典单核细胞(CD14+CD16)亚群的频率降低。在受到TLR4和TLR7/8刺激后,与PWOH相比,PWH的单核细胞和mDCs中TNF-α和IL-1β的产生较低(所有p<0.05)。与PWOH相比,PWH中sCD14水平升高(p = 0.01)表明持续的免疫激活,而与PWH(p = 0.01)和PWH(p = 0.04)相比,PWH中D-二聚体水平升高表明PWH中炎症更高。

结论

PWH表现出与其他PWH类似的免疫反应,包括PWH,其固有免疫特征是单核细胞活化水平较低、经典单核细胞水平降低、产生促炎细胞因子的能力降低以及与不良疾病结局相关的生物标志物升高。这些发现强调了对PWH进行持续监测和潜在治疗干预以减轻慢性炎症的必要性。此外,它扩展了我们对PWH中复杂的固有免疫细胞反应的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ee6/12420260/bb0af1f92d4e/fimmu-16-1603436-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验