Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica, Instituto de Investigaciones en Bacteriología y Virología Molecular (IBaViM), Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Ciudad Autónoma de Buenos Aires, Argentina.
Virology Section, Centro de Educación Médica e Investigaciones Clínicas Norberto Quirno "CEMIC", Buenos Aires, Argentina.
Clin Microbiol Infect. 2022 Oct;28(10):1382-1388. doi: 10.1016/j.cmi.2022.05.009. Epub 2022 May 17.
To compare the homologous prime-boost vaccination scheme of Gam-COVID-Vac (Sputnik V (SpV)) to its heterologous combination with mRNA-1273 (Moderna (Mod)) vaccine.
SARS-CoV-2 anti-spike (S)-receptor binding domain (RBD) IgG concentration was assessed three to seven weeks after complete vaccination. Reactogenicity was evaluated by declared side events and medical assistance required until day 7 post boost.
Of 190 participants enrolled, 105 received homologous SpV/SpV and the remaining heterologous SpV/Mod vaccination scheme, respectively. Median (interquartile range (IQR)) age was 54 (37-63) years, 132 out of 190 (69.5%) were female, and 46 out of 190 (24.2%) individuals had a prior confirmed COVID-19. Anti-S-RBD IgG median (IQR) titers were significantly higher for SpV/Mod (2511 (1476-3992) binding antibody units (BAU)/mL) than for SpV/SpV (582 (209-1609) BAU/mL; p < 0.001] vaccination scheme. In a linear model adjusted for age, gender, time to the serological assay, and time between doses, SpV/Mod (4.154 (6.585-615.554); p < 0.001] and prior COVID (3.732 (8.641-202.010); p < 0.001) were independently associated with higher anti-S-RBD IgG values. A higher frequency of mild and moderate adverse effects was associated with the heterologous scheme (20 of 85 (23.5%) vs. 13 of 105 (12.4%); p = 0.043 and 27 of 85 (31.8%) vs. 14 of 105 (13.3%); p = 0.002), respectively, although it was well tolerated by all individuals and no medical assistance was required.
The heterologous SpV/Mod combination against SARS-CoV-2 is well tolerated and significantly increases humoral immune response as compared to the homologous SpV/SpV immunization.
比较 Gam-COVID-Vac(Sputnik V(SpV))的同源加强免疫接种方案与异源组合 mRNA-1273(Moderna(Mod))疫苗的效果。
在完全接种后 3 至 7 周评估 SARS-CoV-2 抗刺突(S)-受体结合域(RBD)IgG 浓度。通过报告的不良事件和加强针后 7 天内需要的医疗援助来评估不良反应。
190 名入组者中,105 名接受了同源 SpV/SpV 接种方案,其余 85 名接受了异源 SpV/Mod 接种方案。中位(四分位距(IQR))年龄为 54(37-63)岁,190 名中 132 名(69.5%)为女性,46 名(24.2%)为既往确诊 COVID-19 患者。SpV/Mod(2511(1476-3992)结合抗体单位(BAU)/mL)接种方案的抗-S-RBD IgG 中位数(IQR)滴度显著高于 SpV/SpV(582(209-1609)BAU/mL;p<0.001]。在调整年龄、性别、血清学检测时间和剂量间隔的线性模型中,SpV/Mod(4.154(6.585-615.554);p<0.001)和既往 COVID(3.732(8.641-202.010);p<0.001)与更高的抗-S-RBD IgG 值独立相关。与异源方案相关的不良反应频率更高(20/85(23.5%)比 13/105(12.4%);p=0.043 和 27/85(31.8%)比 14/105(13.3%);p=0.002),但所有个体均能耐受,无需医疗援助。
与同源 SpV/SpV 免疫相比,异源 SpV/Mod 组合针对 SARS-CoV-2 的接种具有良好的耐受性,显著增加了体液免疫反应。