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临床试验/NCT07644546
NCT07644546尚未招募不适用

Immunogenicity of MF59-adjuvanted Versus High-dose Influenza Vaccine in People With HIV: a Randomized Clinical Trial

National Taiwan University Hospital0 个研究点目标入组 350 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
350
主要终点
The vaccine response rate among participants undergoing MF59-adjuvanted and high-dose influenza vaccines at day 28

研究概览

简要总结

Seasonal influenza causes morbidity in people with impaired immunity, including adults with elder ages and other comorbidities [1]. Standard-dose inactivated influenza vaccines (IIV) may induce lower hemagglutination inhibition (HAI) titers and more rapid waning in these groups. High-dose IIV could generate higher and more durable serological responses, including HAI, B-cell activation and antibody magnitude, which was demonstrated in randomized trials [2,3]. MF59-adjuvanted IIV further enhances innate immune activation and antigen presentation, potentially broadening and strengthening responses, particularly during antigenic drift seasons [4]. These enhanced platforms represent biologically distinct strategies to overcome reduced vaccine responsiveness.

Influenza A/H3N2 was reported as the predominant circulating strain in Taiwan. Initial antigenic characterization suggested suboptimal match between some circulating A/H3N2 viruses (the subclade K variant) and the vaccine reference strain, whereas A/H1N1 viruses appeared consistency with the circulating and vaccine-containing strain [5]. As of February 2026, approximately 2,300 cases of severe influenza had been confirmed during the 2025-2026 season, representing the largest epidemic in the post-COVID-19 era. In the meanwhile, both MF59-adjuvanted and high-dose influenza vaccine were firstly introduced in Taiwan for elderly people [5].

Previous study had demonstrated that people living HIV (PWH) might have lower humoral immune responses compared with people without HIV, even among PWH with relatively higher (defined as ≥ 350 cells/mm3) CD4 counts [6]. In spite of the broad use of these novel influenza vaccines in older adults and other population with immunocompromised status such as the recipient of solid organ transplantation [7], evidence gap exists in PWH, where vaccine responses vary by CD4 count, viral suppression, immune activation, comorbidities, and prior vaccination history. High-dose influenza vaccination has shown improved serologic outcomes versus standard dose in PWH in randomized trials [2], while data of MF59-adjuvanted vaccines used for PWH are lacking. Moreover, comparative serological responses, durability or effectiveness between the two vaccines (MF59 adjuvant vs high-dose) was only conducted among participants with elder age, which showed that the seroconversion rate for H3N2 among those receiving MF59-adjuvanted vaccines did not meet noninferiority criteria compared with those receiving high-dose vaccines [8]. Nevertheless, such data on PWH remains unclear. In this study, we aimed to compare toe immunogenicity among PWH undergoing MF59-adjuvanted or high-dose seasonal influenza vaccine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •PWH aged ≥18 years

排除标准

  • •History of confirmed severe adverse effects owing to any type of influenza vaccine, including anaphylaxis and Guillain-Barré syndrome.
  • •Severe coagulopathy which causes contraindication for vaccination.
  • •Already vaccinated with any type of 2026-2027 influenza vaccines.
  • •Having diagnosed with influenza one month before vaccination.

研究组 & 干预措施

high-dose vaccine

Active Comparator

干预措施: IM (Biological)

MF59-adjuvant vaccine

Experimental

MF59-adjuvant vaccine

干预措施: IM (Biological)

egg-based vaccine

Active Comparator

干预措施: IM (Biological)

结局指标

主要结局

The vaccine response rate among participants undergoing MF59-adjuvanted and high-dose influenza vaccines at day 28

时间窗: 1 month

The vaccine response rate among participants undergoing MF59-adjuvanted and high-dose influenza vaccines at day 28, defined as the proportion of patients exhibiting seroconversion for at least 1 viral strain (A/H1N1, A/H3N2, or B) contained in the trivalent vaccines at day 28 after vaccination. Seroconversion was defined as a ≥ 4-fold increase of HAI titer from baseline.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

National Taiwan University Clinical Trial Center

Attending Physician

National Taiwan University Hospital

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