Comparison of Two High-Dose Versus Two Standard-Dose Influenza Vaccines in Adult Allogeneic Hematopoietic Cell Transplant Recipients

被引:1
|
作者
Thomas, Lora D. [1 ]
Batarseh, Einas [2 ]
Hamdan, Lubna [2 ]
Haddadin, Zaid [2 ]
Dulek, Daniel [2 ]
Kalams, Spyros [2 ]
Stewart, Laura S. [3 ]
Stahl, Anna L. [2 ]
Rahman, Herdi [2 ]
Amarin, Justin Z. [2 ]
Hayek, Haya [2 ]
Ison, Michael [4 ]
Overton, Edgar T. [5 ]
Pergam, Steven A. [6 ]
Spieker, Andrew J. [7 ]
Halasa, Natasha B. [2 ,8 ]
机构
[1] Virginia Commonwealth Univ, Med Ctr, Dept Med, Richmond, VA USA
[2] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN USA
[3] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[4] NIAID, NIH, Div Microbiol & Infect Dis, Resp Dis Branch, Rockville, MD USA
[5] Univ Alabama Birmingham, Univ Hosp, Dept Med, Birmingham, AL USA
[6] Fred Hutchinson Canc Ctr, Dept Med, Seattle, WA USA
[7] Vanderbilt Univ, Med Ctr, Dept Biostat, Nashville, TN USA
[8] Pediat Infect Dis, Dept Pediat, 1161 21st Ave South,D7235 MCN, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
influenza vaccine; hematopoietic cell transplant; RANDOMIZED-TRIAL; VACCINATION; SAFETY; IMMUNOGENICITY;
D O I
10.1093/cid/ciad458
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Adult hematopoietic cell transplant (HCT) recipients are at high risk for influenza-related morbidity and mortality and have suboptimal influenza vaccine immune responses compared to healthy adults, particularly within 2 years of transplant.Methods This phase II, double-blind, multicenter randomized controlled trial compared 2 doses of high-dose trivalent (HD-TIV) to 2 doses of standard-dose quadrivalent (SD-QIV) influenza vaccine administered 1 month apart in adults 3-23 months post-allogeneic HCT. Hemagglutinin antibody inhibition (HAI) titers were measured at baseline, 4 weeks following each vaccine dose, and approximately 7 months post-second vaccination. Injection-site and systemic reactions were assessed for 7 days post-vaccination. The primary immunogenicity comparison was geometric mean HAI titer (GMT) at visit 3 (4 weeks after the second dose); we used linear mixed models to estimate adjusted GMT ratios (aGMRs) comparing HD-TIV/SD-QIV for each antigen.Results We randomized 124 adults; 64 received SD-QIV and 60 received HD-TIV. Following the second vaccination, HD-TIV was associated with higher GMTs compared to SD-QIV for A/H3N2 (aGMR = 2.09; 95% confidence interval [CI]: [1.19, 3.68]) and B/Victoria (aGMR = 1.61; 95% CI: [1.00, 2.58]). The increase was not statistically significant for A/H1N1 (aGMR = 1.16; 95% CI: [0.67, 2.02]). There was a trend to more injection-site reactions for HD-TIV after the second vaccination compared to SD-QIV (50% vs 33%; adjusted odds ratio [aOR] = 4.53; 95% CI: [0.71, 28.9]), whereas systemic reactions were similar between groups with both injections.Conclusions Adult allogeneic HCT recipients who received 2 doses of HD-TIV produced higher HAI antibody responses for A/H3N2 and B/Victoria compared with 2 doses of SD-QIV, with comparable injection-site or systemic reactions. In this phase II, double-blind, multicenter randomized controlled trial of post-allogeneic hematopoietic cell transplant recipients, 2 doses of high-dose trivalent influenza vaccine had superior immunogenicity than 2 doses of standard-dose quadrivalent influenza vaccine. Graphical abstract This graphical abstract is also available at Tidbit: https://tidbitapp.io/tidbits/comparison-of-two-high-dose-versus-two-standard-dose-influenza-vaccines-in-adult-allogeneic-hematopoietic-cell-transplant-recipients-17b01d1d-6b7c-486f-9645-5d38dbbfeabd
引用
收藏
页码:1723 / 1732
页数:10
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