Immunogenicity of MF59-adjuvanted Versus High-dose Influenza Vaccine in People With HIV: a Randomized Clinical Trial
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.
調査の概要
研究の種類
入学 (推定)
段階
- 適用できない
連絡先と場所
研究連絡先
- 名前:Wang-Da Liu, M.D., M.P.H.
- 電話番号:+886-972-652797
- メール:b95401043@ntu.edu.tw
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- PWH aged ≥18 years
Exclusion Criteria:
- 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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:基礎科学
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:MF59-adjuvant vaccine
|
0.5ml/Vial, IM on Day1
|
|
アクティブコンパレータ:high-dose vaccine
|
0.5ml/Vial, IM on Day1
|
|
アクティブコンパレータ:egg-based vaccine
|
0.5ml/Vial, IM on Day1
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The vaccine response rate among participants undergoing MF59-adjuvanted and high-dose influenza vaccines at day 28
時間枠: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.
|
1 month
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 202603137MIPA
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
HIVの臨床試験
-
Duke UniversityGilead Sciences募集HIV予防 | HIV曝露前予防 | HIV予防プログラム | HIV の予防とケア | HIV 曝露前予防の使用アメリカ
-
Federal University of São PauloGilead Sciences完了
-
University of Alabama at BirminghamMobile County Health Deparment; Alabama Department of Public Health募集HIV | HIV検査 | HIV とケアの関係 | HIV治療アメリカ
-
Institute of HIV Research and Innovation Foundation...National Institutes of Health (NIH)募集
-
University of Alabama at BirminghamNational Institute of Mental Health (NIMH)募集
-
University of PennsylvaniaNational Institute of Mental Health (NIMH); University of Botswana募集
-
French National Agency for Research on AIDS and...Elizabeth Glaser Pediatric AIDS Foundation完了パートナーの HIV 検査 | カップルの HIV カウンセリング | カップルのコミュニケーション | HIV の発生率カメルーン, ドミニカ共和国, グルジア, インド
-
University of Minnesota引きこもったHIV感染症 | HIV/エイズ | HIV | AIDS | エイズ・HIV問題 | エイズと感染症アメリカ
-
Johns Hopkins UniversityNational Institute of Mental Health (NIMH)募集
-
Instituto Mexicano del Seguro Social募集減量 | HIV | HIV-1 感染症 | 体重変化 | HIV アソシエイト減量 | インテグラーゼ阻害剤、HIV; HIVプロテアーゼ阻害剤メキシコ
IMの臨床試験
-
University of Illinois at Chicago完了
-
ImmunAbs Inc.募集重症筋無力症アメリカ, ブルガリア, ポーランド, スペイン, イタリア, セルビア
-
National Institute of Allergy and Infectious Diseases...National Institutes of Health (NIH); Department of Health and Human Services完了
-
STAT Therapeutics IncJohnson County ClinTrials完了