Aiello Anna, Calabrò Anna, Ligotti Mattia Emanuela, Accardi Giulia, Azgomi Mojtaba Shekarkar, Caccamo Nadia, Caruso Calogero, Dieli Francesco, Manna Marco Pio La, Procopio Antonio, Candore Giuseppina
Laboratory of Immunopathology and Immunosenescence, Department of Biomedicine, Neurosciences and Advanced Diagnostics, University of Palermo, 90127, Palermo, Italy.
Department of Research, Mediterranean Institute for Transplantation and Advanced Specialized Therapies (IRCCS-ISMETT), 90127, Palermo, Italy.
Immun Ageing. 2025 Mar 26;22(1):13. doi: 10.1186/s12979-025-00506-y.
Aging is frequently characterized by an inadequate primary vaccine response, likely due to immunosenescence and inflamm-aging, a low-level, chronic inflammatory state. Both aspects increase the susceptibility of older adults to viral and bacterial infections, resulting in a higher frequency and severity of infectious diseases. In this preliminary study, a cohort of 52 individuals was recruited and divided into two groups: young (age range 21-35) and older adults (> 60 years old). Peripheral blood mononuclear cells (PBMCs) were collected before (time 0, T0) and after (time 1, T1) the immunization with a tetravalent influenza vaccine. Then, T cell immunophenotyping analysis was conducted to investigate how aging and influenza vaccination influence T cell responses. Additionally, the anti-inflammatory and antioxidant effects of oleuropein (OLE), a secoiridoid extracted from extra virgin olive oil, alone or in combination with BIRB 796, a potent inhibitor of p38 MAPK, were explored to enhancing the impact of influenza virus on T cell activation, aiming to identify potential alternatives or complementary strategies to improve traditional flu-vaccine formulations. Statistically significant observations were noted for a decrement in CD8 + T naïve and an increase of effector memory between the young and older adults after flu-vaccination. Moreover, preliminary findings indicate anti-inflammatory and antioxidant properties of OLE and BIRB 796 on T cell responses, particularly regarding Reactive Oxygen Species/Reactive Nitrogen Species modulation, with a trend toward the decrease of pro-inflammatory cytokines (i.e., Interferon-γ (INF-γ), Tumor Necrosis Factor-α (TNF-α)), αalthough without statistical significance.
衰老的特征通常是初次疫苗反应不足,这可能是由于免疫衰老和炎症衰老(一种低水平的慢性炎症状态)所致。这两个方面都会增加老年人对病毒和细菌感染的易感性,导致传染病的发病率和严重程度更高。在这项初步研究中,招募了52名个体并将其分为两组:年轻人(年龄范围21 - 35岁)和老年人(> 60岁)。在接种四价流感疫苗之前(时间0,T0)和之后(时间1,T1)收集外周血单核细胞(PBMC)。然后,进行T细胞免疫表型分析,以研究衰老和流感疫苗接种如何影响T细胞反应。此外,还探讨了橄榄苦苷(OLE,一种从特级初榨橄榄油中提取的裂环环烯醚萜)单独或与p38丝裂原活化蛋白激酶(MAPK)的强效抑制剂BIRB 796联合使用时的抗炎和抗氧化作用,以增强流感病毒对T细胞活化的影响,旨在确定改善传统流感疫苗配方的潜在替代或补充策略。接种流感疫苗后,年轻人和老年人之间的CD8 + 初始T细胞减少以及效应记忆细胞增加,差异具有统计学意义。此外,初步研究结果表明,OLE和BIRB 796对T细胞反应具有抗炎和抗氧化特性,特别是在活性氧/活性氮调节方面,促炎细胞因子(即干扰素 - γ(INF - γ)、肿瘤坏死因子 - α(TNF - α))有下降趋势,尽管无统计学意义。