Immunogenicity of High-Dose Versus MF59-Adjuvanted Versus Standard Influenza Vaccine in Solid Organ Transplant Recipients: The Swiss/Spanish Trial in Solid Organ Transplantation on Prevention of Influenza (STOP-FLU Trial)

Matteo Mombelli,Dionysios Neofytos,Uyen Huynh-Do, Javier Sanchez-Cespedes,Susanne Stampf, Dela Golshayan,Suzan Dahdal, Guido Stirnimann,Aurelia Schnyder, Christian Garzoni, Reto M. Venzin,Lorenzo Magenta, Melanie Schonenberger, Laura Walti,Cedric Hirzel, Aline Munting,Michael Dickenmann, Michael Koller,John-David Aubert, Jurg Steiger,Manuel Pascual, Thomas F. Mueller,Mace Schuurmans, Christoph Berger,Isabelle Binet, Jean Villard,Nicolas J. Mueller, Adrian Egli,Elisa Cordero, Christian van Delden,Oriol Manuel

CLINICAL INFECTIOUS DISEASES(2024)

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摘要
Background. The immunogenicity of the standard influenza vaccine is reduced in solid-organ transplant (SOT) recipients, so new vaccination strategies are needed in this population.Methods. Adult SOT recipients from 9 transplant clinics in Switzerland and Spain were enrolled if they were >3 months after transplantation. Patients were randomized (1:1:1) to a MF59-adjuvanted or a high-dose vaccine (intervention), or a standard vaccine (control), with stratification by organ and time from transplant. The primary outcome was vaccine response rate, defined as a =4-fold increase of hemagglutination-inhibition titers to at least 1 vaccine strain at 28 days postvaccination. Secondary outcomes included polymerase chain reaction-confirmed influenza and vaccine reactogenicity.Results. A total of 619 patients were randomized, 616 received the assigned vaccines, and 598 had serum available for analysis of the primary endpoint (standard, n = 198; MF59-adjuvanted, n = 205; high-dose, n = 195 patients). Vaccine response rates were 42% (84/ 198) in the standard vaccine group, 60% (122/205) in the MF59-adjuvanted vaccine group, and 66% (129/195) in the high-dose vaccine group (difference in intervention vaccines vs standard vaccine, 0.20; 97.5% confidence interval [CI], .12-1); P < .001; difference in high-dose vs standard vaccine, 0.24 [95% CI, .16-1]; P < .001; difference in MF59-adjuvanted vs standard vaccine, 0.17 [97.5% CI, .08-1]; P < .001). Influenza occurred in 6% of the standard, 5% in the MF59-adjuvanted, and 7% in the high-dose vaccine groups. Vaccine-related adverse events occurred more frequently in the intervention vaccine groups, but most of the events were mild.Conclusions. In SOT recipients, use of an MF59-adjuvanted or a high-dose influenza vaccine was safe and resulted in a higher vaccine response rate.
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关键词
influenza,immunocompromised,vaccination,transplantation
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