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

Abstract 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, m...

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Veröffentlicht in:Clinical infectious diseases 2023-12, Vol.77 (12), p.1723-1732
Hauptverfasser: Thomas, Lora D, Batarseh, Einas, Hamdan, Lubna, Haddadin, Zaid, Dulek, Daniel, Kalams, Spyros, Stewart, Laura S, Stahl, Anna L, Rahman, Herdi, Amarin, Justin Z, Hayek, Haya, Ison, Michael, Overton, Edgar T, Pergam, Steven A, Spieker, Andrew J, Halasa, Natasha B
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Zusammenfassung:Abstract 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 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
ISSN:1058-4838
1537-6591
1537-6591
DOI:10.1093/cid/ciad458