Venuto Roberto, Giunta Ioselita, Vaccaro Mario, La Fauci Vincenza, Ceccio Concetta, Fedele Francesco, Privitera Antonino, Denaro Federica, Pantò Giuseppe, Cortese Rosaria, Visalli Giovanna, D'Amato Smeralda, Squeri Andrea, Squeri Raffaele, Genovese Cristina
Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, 98124 Messina, Italy.
Department of Clinical and Experimental Medicine, Unit of Dermatology, University of Messina, 98124 Messina, Italy.
Vaccines (Basel). 2022 Oct 26;10(11):1803. doi: 10.3390/vaccines10111803.
On 11 June 2021, the Italian Ministry of Health authorized the heterologous vaccination schedule. The goals of our retrospective study were to (a) evaluate the undesirable effects after the administration of Vaxzevria and Comirnaty vaccines; (b) evaluate the antibody response after 28 days from the administration of the second dose; and (c) compare the antibody responses after the homologous and heterologous vaccination regimens. The undesirable effects were collected using a survey; IgG Spike was quantified using the electrochemiluminescence method; the comparison between the antibody responses was carried out using the sample of a homologous vaccine schedule previously analyzed. Pain at the injection site is the most common undesirable effect after the administration of both vaccines (62.1% after Vaxzevria vs. 82.75% after Comirnaty); swelling at the injection site is more frequent after the administration of Vaxzevria than after the administration of Comirnaty: (15.52% vs. 5.17%); headache is more frequent in women than in men for both the vaccination types (p < 0.05); 49.09% of the sample reported IgG Spike ≥ 12,500 U/mL; the antibody titer of the heterologous schedule is higher than that of the homologous vaccination. Our study demonstrated that the undesirable effects after the administration of the second dose are less frequent and less severe than after the administration of the first dose, and that the immunogenicity of the heterologous vaccinations is higher than that of the homologous ones.
2021年6月11日,意大利卫生部批准了异源疫苗接种方案。我们这项回顾性研究的目的是:(a)评估接种阿斯利康疫苗和辉瑞疫苗后的不良反应;(b)评估第二剂接种28天后的抗体反应;(c)比较同源和异源疫苗接种方案后的抗体反应。通过一项调查收集不良反应;采用电化学发光法对IgG刺突蛋白进行定量;使用先前分析的同源疫苗接种方案样本对抗体反应进行比较。两种疫苗接种后,注射部位疼痛是最常见的不良反应(接种阿斯利康疫苗后为62.1%,接种辉瑞疫苗后为82.75%);接种阿斯利康疫苗后注射部位肿胀比接种辉瑞疫苗后更常见(分别为15.52%和5.17%);两种疫苗接种类型中,女性头痛的发生率均高于男性(p<0.05);49.09%的样本报告IgG刺突蛋白≥12,500 U/mL;异源接种方案的抗体滴度高于同源接种。我们的研究表明,第二剂接种后的不良反应比第一剂接种后更少见、更轻微,并且异源接种的免疫原性高于同源接种。