Unninayar Dana, Falcone Emilia L, Chapdelaine Hugo, Vinh Donald C, Top Karina A, Derfalvi Beata, Issekutz Thomas B, Decaluwe Hélène, Pham-Huy Anne, Upton Julia, Betschel Stephen D, Rubin Tamar, Suresh Sneha, Wright Nicola A M, Murguía-Favela Luis, Kalashnikova Tatiana, Barrett Lisa, Oldford Sharon, Langlois Marc-Andre, Arnold Corey, Sadarangani Manish, Zhang Tinghua, Ramsay Tim, Yazji Dina, Cowan Juthaporn
Inflammation and Chronic Disease Program, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.
Department of Medicine, Centre Hospitalier de l'Université de Montréal, Montreal, QC, Canada.
Front Immunol. 2025 Jan 21;15:1501908. doi: 10.3389/fimmu.2024.1501908. eCollection 2024.
Many individuals with inborn errors of immunity (IEIs) have poor humoral immune (HI) vaccine responses. Only a few studies have examined specific cell-mediated immune (CMI) responses to coronavirus disease 2019 (COVID-19) vaccines in this population. Therefore, the purpose of this study was to examine HI and CMI responses up to 6 months post-COVID-19 vaccine dose 3 in adults with IEIs.
A multi-center prospective observational study was conducted across Canada to collect severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2)-specific HI and CMI data at 4- and 24-week intervals after vaccine doses 2 and 3 (D2 + 4wk/D2 + 24wk/D3 + 4wk/D3 + 24wk).
A total of 149 adults with IEIs and 423 healthy controls were recruited from July 2021 to October 2023. Geometric mean anti-spike IgG (binding antibody units/mL) and spike-specific T-cell responses [IFN-γ T cells/10 peripheral blood mononuclear cells (PBMCs)] were significantly lower in IEIs compared to controls at D2 + 4wk, D3 + 4wk, and D3 + 24wk. However, at 6 months after completing the primary series (three doses for IEIs and two doses for healthy), both HI and CMI responses of both IEI participants and healthy controls persisted and were comparable. There was a strong correlation between neutralizing antibody titer (ID50) and anti-spike IgG but not between ID50 and CMI. There was only one reported case of hospitalized COVID-19 disease before and none after completing the primary series among IEI participants.
Adults with IEIs mounted both HI and CMI responses following COVID-19 vaccines, which were lower than those of healthy individuals but were present at least up to 6 months after dose 3. These data support the initial recommendation for a three-dose primary series among IEIs.
许多患有先天性免疫缺陷(IEIs)的个体对体液免疫(HI)疫苗的反应较差。只有少数研究检测了该人群对2019冠状病毒病(COVID-19)疫苗的特异性细胞介导免疫(CMI)反应。因此,本研究的目的是检测患有IEIs的成年人在接种第三剂COVID-19疫苗后6个月内的HI和CMI反应。
在加拿大开展了一项多中心前瞻性观察性研究,在接种第二剂和第三剂疫苗后的第4周和第24周(D2 + 4周/D2 + 24周/D3 + 4周/D3 + 24周)收集严重急性呼吸综合征冠状病毒2(SARS-CoV-2)特异性HI和CMI数据。
2021年7月至2023年10月,共招募了149名患有IEIs的成年人和423名健康对照。在D2 + 4周、D3 + 4周和D3 + 24周时,IEIs患者的几何平均抗刺突IgG(结合抗体单位/毫升)和刺突特异性T细胞反应[IFN-γ T细胞/10个外周血单个核细胞(PBMC)]显著低于对照组。然而,在完成初始系列接种后6个月(IEIs患者接种三剂,健康对照接种两剂),IEIs参与者和健康对照的HI和CMI反应均持续存在且相当。中和抗体滴度(ID50)与抗刺突IgG之间存在强相关性,但ID50与CMI之间无相关性。在IEIs参与者中,接种初始系列疫苗之前报告了1例COVID-19住院病例,之后无病例报告。
患有IEIs的成年人在接种COVID-19疫苗后产生了HI和CMI反应,虽然低于健康个体,但至少在第三剂接种后6个月仍存在。这些数据支持了最初关于IEIs患者接种三剂初始系列疫苗的建议。