Kundura Lucy, Cezar Renaud, Gimenez Sandrine, Pastore Manuela, Reynes Christelle, Sotto Albert, Reynes Jacques, Allavena Clotilde, Meyer Laurence, Makinson Alain, Corbeau Pierre
Institute of Human Genetics, CNRS-Montpellier University UMR9002, 141 rue de la Cardonille, Montpellier, 34396, France.
Immunology Department, Nîmes University Hospital, Place du Pr Debré, Nîmes, 30029, France.
Immun Ageing. 2024 Mar 13;21(1):20. doi: 10.1186/s12979-024-00416-5.
People living with HIV (PLWH) are at risk of frailty, which is predictive for death. As an overactivity of the immune system is thought to fuel frailty, we characterized the immune activation profiles linked to frailty.
We quantified twenty-seven activation markers in forty-six virological responders (four females and forty-two males; median age, 74 years; median duration of infection, 24 years; median duration of undetectability, 13 years), whose frailty was determined according to the Fried criteria. T cell and NK cell activation was evaluated by flow cytometry, using a panel of cell surface markers. Soluble markers of inflammation, and monocyte activation and endothelial activation were measured by ELISA. The participants' immune activation was profiled by an unsupervised double hierarchical clustering analysis. We used ANOVA p-values to rank immunomarkers most related to Fried score. A Linear Discriminant Analysis (LDA) was performed to link immune activation markers to frailty.
41% of the participants were pre-frail, including 24% with a Fried score of 1, and 17% with a Fried score of 2. ANOVA identified the 14 markers of T cell, monocyte, NK cell, endothelial activation, and inflammation the most linked to Fried 3 classes. The LDA performed with these 14 markers was capable of discriminating volunteers according to their Fried score. Two out of the 5 immune activation profiles revealed by the hierarchical clustering were linked to and predictive of pre-frailty. These two profiles were characterized by a low percentage of CD4 T cells and a high percentage of CD8 T cells, activated CD4 T cells, CD8 T cells, and NK cells, and inflammation.
We identified a particular immune activation profile associated with pre-frailty in PLWH. Profiling participants at risk of developing frailty might help to tailor the screening and prevention of medical complications fueled by loss of robustness. Further studies will indicate whether this frailty signature is specific or not of HIV infection, and whether it also precedes frailty in the general population.
人类免疫缺陷病毒感染者(PLWH)存在虚弱风险,而虚弱可预测死亡。由于免疫系统过度活跃被认为会加剧虚弱,我们对与虚弱相关的免疫激活谱进行了特征分析。
我们对46名病毒学应答者(4名女性和42名男性;年龄中位数74岁;感染持续时间中位数24年;病毒载量不可测持续时间中位数13年)的27种激活标志物进行了定量分析,这些应答者的虚弱状况根据弗里德标准确定。通过流式细胞术,使用一组细胞表面标志物评估T细胞和NK细胞的激活情况。通过酶联免疫吸附测定法测量炎症的可溶性标志物、单核细胞激活和内皮激活情况。通过无监督双层次聚类分析对参与者的免疫激活情况进行分析。我们使用方差分析p值对与弗里德评分最相关的免疫标志物进行排名。进行线性判别分析(LDA)以将免疫激活标志物与虚弱联系起来。
41%的参与者处于虚弱前期,其中24%的弗里德评分为1分,17%的弗里德评分为2分。方差分析确定了与弗里德3类最相关的14种T细胞、单核细胞、NK细胞、内皮激活和炎症标志物。用这14种标志物进行的线性判别分析能够根据弗里德评分区分志愿者。层次聚类揭示的5种免疫激活谱中有2种与虚弱前期相关且可预测虚弱前期。这两种谱的特征是CD4 T细胞百分比低,而CD8 T细胞、活化的CD4 T细胞、CD8 T细胞和NK细胞以及炎症的百分比高。
我们在PLWH中确定了一种与虚弱前期相关的特定免疫激活谱。对有发展为虚弱风险的参与者进行分析可能有助于定制针对因身体机能下降引发的医疗并发症的筛查和预防措施。进一步的研究将表明这种虚弱特征是否特定于HIV感染,以及它是否也先于普通人群的虚弱出现。