Fukushima Kiyoyasu, Kubo Toru, Ito Yuta, Oda Yoshie, Nagayoshi Yohsuke, Fukuda Minoru, Takazono Takahiro, Sakamoto Noriho, Mukae Hiroshi
Department of Respiratory Medicine, Japanese Red Cross Nagasaki Genbaku Isahaya Hospital, 986-2 Keya Tarami-cho Isahaya City, Nagasaki, 859-0497, Japan.
Department of Laboratory Medicine, Japanese Red Cross Nagasaki Genbaku Isahaya Hospital, 986-2 Keya Tarami-cho Isahaya City, Nagasaki, 859-0497, Japan.
J Infect Chemother. 2025 Jun;31(6):102695. doi: 10.1016/j.jiac.2025.102695. Epub 2025 Apr 4.
This study examined the durability of humoral and cell-mediated immune responses to COVID-19 mRNA vaccines over six months, focusing on age-related changes.
SARS-CoV-2 uninfected Japanese subjects aged 20-99 who received two doses of mRNA COVID-19 vaccine were recruited. SARS-CoV-2 Spike IgG antibody (IgG) level in the serum and the levels of interferon (IFN)-γ in blood stimulated with SARS-CoV-2 specific antigens by QuantiFERON (QFN) SARS-CoV-2 assay were measured.
The IgG levels of 138 subjects declined significantly with age and time post-vaccination (p < 0.001). For participants aged 70 and above (n = 80), the IFN-γ levels, an indicator of cell-mediated immunity, also significantly declined over time (p < 0.05). However, in those under 70 (n = 58), the IFN-γ levels were maintained at three- and six months post-vaccination. There was no significant difference in IFN-γ levels between three- and six months post-vaccination for all 138 subjects, including CD4 and CD8 T cell counts. No correlation was observed between IgG antibody levels and secreted IFN-γ values. Multivariate regression analysis revealed a significant correlation between IgG levels and age. In contrast, IFN-γ levels were associated with CD4 T cell counts, CD8 T cell counts, and Performance Status Scores but not with age.
The findings suggest that while humoral immunity (IgG levels) decreases with age and time, cell-mediated immunity (IFN-γ levels) is relatively preserved in individuals under 70 up to six months post-vaccination. However, this immune response is significantly attenuated in older adults aged 70 and above, indicating age-related immunosenescence in long-term immunity following COVID-19 vaccination.
本研究检测了6个月内针对新冠病毒mRNA疫苗的体液免疫和细胞介导免疫反应的持久性,重点关注与年龄相关的变化。
招募了20-99岁未感染新冠病毒的日本受试者,他们接种了两剂新冠病毒mRNA疫苗。检测血清中新冠病毒刺突蛋白IgG抗体(IgG)水平以及通过QuantiFERON(QFN)新冠病毒检测法用新冠病毒特异性抗原刺激血液后干扰素(IFN)-γ水平。
138名受试者的IgG水平随年龄和接种后时间显著下降(p<0.001)。对于70岁及以上的参与者(n=80),作为细胞介导免疫指标的IFN-γ水平也随时间显著下降(p<0.05)。然而,在70岁以下的人群中(n=58),接种后3个月和6个月时IFN-γ水平保持稳定。在所有138名受试者中,接种后3个月和6个月时IFN-γ水平(包括CD4和CD8 T细胞计数)无显著差异。未观察到IgG抗体水平与分泌的IFN-γ值之间存在相关性。多变量回归分析显示IgG水平与年龄之间存在显著相关性。相比之下,IFN-γ水平与CD4 T细胞计数、CD8 T细胞计数和体能状态评分相关,但与年龄无关。
研究结果表明,虽然体液免疫(IgG水平)随年龄和时间下降,但在70岁以下人群中,接种后长达6个月细胞介导免疫(IFN-γ水平)相对保持稳定。然而,在70岁及以上的老年人中,这种免疫反应显著减弱,表明新冠病毒疫苗接种后长期免疫中存在与年龄相关的免疫衰老。