De La Torre Tarazona Erick, Moraga Elisa, Fons-Contreras María, Vaquer Raúl, Sánchez-Palomino Sonsoles, Vallejo-Palma Germán, Calderón-Vicente Sergio, Vicens-Artés Sònia, Aldamiz-Echevarria Teresa, Ciudad Sañudo Marianela, Moreno Cristina, Armenteros-Yeguas Inés, Tiraboschi Juan, Reus Bañuls Sergio, Alcamí José, Serrano-Villar Sergio, Moreno Santiago
Infectious Diseases Department, Hospital Universitario Ramón y Cajal, Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), 28034 Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Infecciosas (CIBERINFEC), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Int J Mol Sci. 2025 Aug 29;26(17):8430. doi: 10.3390/ijms26178430.
The dynamics of the HIV reservoir during antiretroviral therapy (ART) exhibit variability, with a pronounced decline during the initial years of treatment. However, the identification of biomarkers and host factors associated with the decay of the different forms of HIV proviruses remains to be fully elucidated. We conducted a longitudinal study on people with HIV provided by the Spanish National HIV cohort. We assessed the HIV-DNA levels by Intact Proviral DNA Assay, and inflammatory markers using the Proximity Extension Assay, before and after ART initiation. A multivariate linear regression model was employed to identify potential predictive markers. Our results highlight the identification of novel inflammatory markers, such as ADA, DNER, CDCP1, SCF, among others, that varied significantly over ART initiation. In addition, we observed several markers associated with intact HIV-DNA before ART initiation (CD8A, CX3CL1, and ST1A1) or during undetectable viral load post-ART (IL-10). Moreover, up to five markers were able to predict the intact HIV reservoir decay over ART. The strongest predictor was Stem Cell Factor (SCF), where higher baseline levels of this marker were associated with a greater decline in the intact HIV reservoir. In conclusion, we have identified inflammatory markers associated with the size and dynamics of the HIV-DNA reservoir. These findings provide new insights that could contribute to the development of multi-targeted intervention strategies aimed at modulating or monitoring the HIV reservoir size.
抗逆转录病毒疗法(ART)期间HIV储存库的动态变化存在差异,在治疗的最初几年会有明显下降。然而,与不同形式HIV前病毒衰变相关的生物标志物和宿主因素仍有待充分阐明。我们对西班牙国家HIV队列提供的HIV感染者进行了一项纵向研究。在ART开始前后,我们通过完整前病毒DNA检测评估HIV-DNA水平,并使用邻位延伸分析评估炎症标志物。采用多元线性回归模型来识别潜在的预测标志物。我们的结果突出了对新型炎症标志物的识别,如ADA、DNER、CDCP1、SCF等,这些标志物在ART开始后有显著变化。此外,我们观察到在ART开始前(CD8A、CX3CL1和ST1A1)或ART后病毒载量不可检测期间(IL-10)与完整HIV-DNA相关的几种标志物。此外,多达五种标志物能够预测ART期间完整HIV储存库的衰变。最强的预测因子是干细胞因子(SCF),该标志物较高的基线水平与完整HIV储存库的更大下降相关。总之,我们已经识别出与HIV-DNA储存库大小和动态变化相关的炎症标志物。这些发现提供了新的见解,可能有助于制定旨在调节或监测HIV储存库大小的多靶点干预策略。