State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, Fujian, China.
Department of Immunization Program, Taizhou Municipal Center for Disease Control and Prevention, Taizhou, Zhejiang, China.
Hum Vaccin Immunother. 2022 Nov 30;18(5):2071061. doi: 10.1080/21645515.2022.2071061. Epub 2022 Jun 10.
Yearly administration of influenza vaccine with recommendations can help control seasonal influenza epidemics in adults aged ≥60 years. Here, we describe the results of a prospective study observing the immunogenicity and persistence of induced immunity of a trivalent inactivated split-virion influenza vaccine (TIV) in adults aged ≥60 years during the 2018-2019 season in Taizhou City, Zhejiang Province in China. A total of 422 participants completed the study period. Vaccinated participants (284) received a single dose of TIV, but unvaccinated participants (138) didn't receive any vaccine. Study participants vaccinated with TIV had significantly higher GMTs of Hemagglutination Inhibition (HI) antibodies against AH1N1, AH2N3, and B/Victoria strains (all < .0001) at day 30 post-vaccination compared with unvaccinated participants, but the antibody response to the B/Victoria strain was the weakest. Rates of seroprotection and seroconversion were generally higher in the TIV-vaccinated group. At day 180 post-vaccination, the seroconversion rates (95%CI) in the vaccinated group were 99.6% (99.0%-100.3%), 97.9% (96.2%-99.6%), and 68.3% (62.9%-73.8%) for antibodies against three influenza strains, respectively; these rates were significantly different compared with unvaccinated group only for strains AH3N2 and B/Victoria ( = .002 and < .0001, respectively). These results confirm that in adults aged ≥60 years, a single dose of TIV can induce a protective immune response against influenza, but the protective HI antibody levels induced against strain B/Victoria do not persist through 6 months.
每年接种流感疫苗并遵循相关建议有助于控制 60 岁及以上成年人的季节性流感流行。在此,我们描述了一项前瞻性研究的结果,该研究观察了在中国浙江省台州市 2018-2019 年季节中,三价灭活分裂病毒流感疫苗(TIV)在 60 岁及以上成年人中的免疫原性和诱导免疫持久性。共有 422 名参与者完成了研究期。接种疫苗的参与者(284 名)接受了一剂 TIV,但未接种疫苗的参与者(138 名)未接种任何疫苗。接种 TIV 的研究参与者在接种后第 30 天针对 AH1N1、AH2N3 和 B/Victoria 株的血凝抑制(HI)抗体几何平均滴度(GMT)明显更高(均 < .0001),与未接种疫苗的参与者相比,但对 B/Victoria 株的抗体反应最弱。TIV 疫苗接种组的血清保护率和血清转化率通常较高。接种后第 180 天,疫苗接种组的血清转化率(95%CI)分别为针对三种流感株的 99.6%(99.0%-100.3%)、97.9%(96.2%-99.6%)和 68.3%(62.9%-73.8%);与未接种疫苗的组相比,这些比率仅针对 A/H3N2 和 B/Victoria 株差异显著( = .002 和 < .0001)。这些结果证实,在 60 岁及以上成年人中,一剂 TIV 可以诱导针对流感的保护性免疫应答,但针对 B/Victoria 株诱导的保护性 HI 抗体水平不会持续 6 个月。