Kavian Niloufar, Hachim Asmaa, Li Athena Py, Cohen Carolyn A, Chin Alex Wh, Poon Leo Lm, Fang Vicky J, Leung Nancy Hl, Cowling Benjamin J, Valkenburg Sophie A
HKU-Pasteur Research Pole School of Public Health The University of Hong Kong Hong Kong.
World Health Organization Collaborating Centre for Infectious Disease Epidemiology and Control School of Public Health The University of Hong Kong Hong Kong.
Clin Transl Immunology. 2020 Feb 3;9(2):e1107. doi: 10.1002/cti2.1107. eCollection 2020.
Enhanced inactivated influenza vaccines (eIIV) aim to increase immunogenicity and protection compared with the widely used standard IIV (S-IIV).
We tested four vaccines in parallel, FluZone high dose, FluBlok and FluAd versus S-IIV in a randomised controlled trial of older adults and in a mouse infection model to assess immunogenicity, protection from lethal challenge and mechanisms of action.
In older adults, FluAd vaccination stimulated a superior antibody profile, including H3-HA antibodies that were elevated for up to 1 year after vaccination, higher avidity H3HA IgG and larger HA stem IgG responses. In a mouse model, FluAd also elicited an earlier and larger induction of HA stem antibodies with increased germinal centre responses and upregulation and long-term expression of B-cell switch transcription factors. Long-term cross-reactive memory responses were sustained by FluAd following lethal heterosubtypic influenza challenge, with reduced lung damage and viral loads, coinciding with increased T- and B-cell recall. Advantages were also noted for the high-dose FluZone vaccine in both humans and mice.
The early, broadly reactive and long-lived antibody response of FluAd indicates a potential advantage of this vaccine, particularly in years when there is a mismatch between the vaccine strain and the circulating strain of influenza viruses.
与广泛使用的标准灭活流感疫苗(S-IIV)相比,增强型灭活流感疫苗(eIIV)旨在提高免疫原性和保护作用。
我们在一项针对老年人的随机对照试验和小鼠感染模型中,对四种疫苗(FluZone高剂量疫苗、FluBlok疫苗和FluAd疫苗)与S-IIV进行了平行测试,以评估免疫原性、对致死性攻击的保护作用及作用机制。
在老年人中,接种FluAd疫苗激发了更优的抗体反应,包括接种后长达1年仍维持升高的H3-HA抗体、更高亲和力的H3HA IgG以及更强的HA茎部IgG反应。在小鼠模型中,FluAd疫苗还能更早且更强烈地诱导HA茎部抗体产生,生发中心反应增加,B细胞转换转录因子上调并长期表达。在致死性异型流感病毒攻击后,FluAd疫苗能维持长期的交叉反应性记忆反应,减轻肺部损伤并降低病毒载量,同时T细胞和B细胞的回忆反应增强。在人和小鼠中,高剂量FluZone疫苗也显示出优势。
FluAd疫苗早期、广泛反应且持久的抗体反应表明该疫苗具有潜在优势,尤其是在疫苗株与流感病毒流行株不匹配的年份。