Gelderloos Anne T, Verheul Marije K, Middelhof Irene, de Zeeuw-Brouwer Mary-Lène, van Binnendijk Robert S, Buisman Anne-Marie, van Kasteren Puck B
Center for Immunology of Infectious Diseases and Vaccines (IIV), Center for Infectious Disease Control, National Institute for Public Health and the Environment (RIVM), Bilthoven, the Netherlands.
Immun Ageing. 2024 Sep 14;21(1):63. doi: 10.1186/s12979-024-00466-9.
Previous research has shown that repeated COVID-19 mRNA vaccination leads to a marked increase of SARS-CoV-2 spike-specific serum antibodies of the IgG4 subclass, indicating far-reaching immunoglobulin class switching after booster immunization. Considering that repeated vaccination has been recommended especially for older adults, the aim of this study was to investigate IgG subclass responses in the ageing population and assess their relation with Fc-mediated antibody effector functionality.
Spike S1-specific IgG subclass concentrations (expressed in arbitrary units per mL), antibody-dependent NK cell activation, complement deposition and monocyte phagocytosis were quantified in serum from older adults (n = 38-50, 65-83 years) at one month post-second, -third and -fifth vaccination. Subclass distribution in serum was compared to that in younger adults (n = 64, 18-47 years) at one month post-second and -third vaccination. Compared to younger individuals, older adults showed increased levels of IgG2 and IgG4 at one month post-third vaccination (possibly related to factors other than age) and a further increase following a fifth dose. The capacity of specific serum antibodies to mediate NK cell activation and complement deposition relative to S1-specific total IgG concentrations decreased upon repeated vaccination. This decrease associated with an increased IgG4/IgG1 ratio.
In conclusion, these findings show that, like younger individuals, older adults produce antibodies with reduced functional capacity upon repeated COVID-19 mRNA vaccination. Additional research is needed to better understand the mechanisms underlying these responses and their potential implications for vaccine effectiveness. Such knowledge is vital for the future design of optimal vaccination strategies in the ageing population.
先前的研究表明,重复接种新冠病毒mRNA疫苗会导致IgG4亚类的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突特异性血清抗体显著增加,这表明加强免疫后发生了广泛的免疫球蛋白类别转换。鉴于尤其建议老年人重复接种疫苗,本研究的目的是调查老年人群中的IgG亚类反应,并评估它们与Fc介导的抗体效应功能的关系。
在第二次、第三次和第五次接种疫苗后1个月,对老年人(n = 38 - 50,65 - 83岁)血清中的刺突S1特异性IgG亚类浓度(以每毫升任意单位表示)、抗体依赖性自然杀伤(NK)细胞活化、补体沉积和单核细胞吞噬作用进行了定量。将血清中的亚类分布与第二次和第三次接种疫苗后1个月的年轻人(n = 64,1 ... 47岁)进行了比较。与年轻人相比,老年人在第三次接种疫苗后1个月时IgG2和IgG4水平升高(可能与年龄以外的因素有关),在第五剂接种后进一步升高。相对于S1特异性总IgG浓度,重复接种疫苗后特异性血清抗体介导NK细胞活化和补体沉积的能力下降。这种下降与IgG4/IgG1比值增加有关。
总之,这些发现表明,与年轻人一样,老年人在重复接种新冠病毒mRNA疫苗后产生的抗体功能能力降低。需要进一步研究以更好地了解这些反应的潜在机制及其对疫苗效力的潜在影响。这些知识对于未来老年人群最佳疫苗接种策略的设计至关重要。