作者
Jessie R. Chung,Ashley Price,Richard K. Zimmerman,Krissy Moehling Geffel,Stacey L. House,Tara Curley,Karen J. Wernli,C. Hallie Phillips,Emily T. Martin,Ivana A. Vaughn,Vel Murugan,Matthew Scotch,Elie Saade,Kiran A. Faryar,Manjusha Gaglani,Jason D. Ramm,Olivia L. Williams,Emmanuel B. Walter,Marie K. Kirby,Lisa M. Keong,Rebecca Kondor,Sascha Ellington,Brendan Flannery,Joanna L. Kramer,Minal Patel,Lora Nordstrom,Mary Mulrow,Steven C. Holland,Temitope O. C. Faleye,Arnold S. Monto,Darren W. Hearn,Caroline Cheng,Lois Lamerato,Jean Ashley Lava,Md Musharraf Hossain,Michael Lehmkuhl,Elizabeth Capasso-Gulve,James L. Mills,Joshua Jackson,Natalie A.B. Bontrager,Darren J Morrow,Wes Rountree,Christopher A. Todd,Cameron R. Wolfe,Robert A. Salata,Kirk A. Stiffler,Jason J Glagola,Zainab Albar,Christopher Ladikos,Curtis J. Donskey,Mary Patricia Nowalk,G.K. Balasubramani,Tracey Conti,David A Figucia,John V. Williams,Alexandra Weissman,Spencer Rose,Michael Smith,Leah Odame‐Bamfo,Kempapura Murthy,Chandni Raiyani,Mufaddal Mamawala,Erika Kiniry,Brianna Wickersham,Rachael P Doud,Matthew Nguyen,Juliana DaSilva,S. Tucker Sheffield,Julia C. Frederick,Malania M. Wilson,Ewelina Lyszkowicz,Philip Shirk
摘要
The 2023-24 U.S. influenza season was characterized by a predominance of A(H1N1)pdm09 virus circulation with co-circulation of A(H3N2) and B/Victoria viruses. We estimated vaccine effectiveness (VE) in the United States against mild-to-moderate medically attended influenza illness in the 2023-24 season. We enrolled outpatients aged ≥8 months with acute respiratory illness in 7 states. Respiratory specimens were tested for influenza type/subtype by reverse-transcriptase polymerase chain reaction (RT-PCR). Influenza VE was estimated with a test-negative design comparing odds of testing positive for influenza among vaccinated versus unvaccinated participants. We estimated VE by virus sub-type/lineage and A(H1N1)pdm09 genetic subclades. Among 6,589 enrolled patients, 1,770 (27%) tested positive for influenza including 796 A(H1N1)pdm09, 563 B/Victoria, and 323 A(H3N2). Vaccine effectiveness against any influenza illness was 41% (95% Confidence Interval [CI]: 32 to 49): 28% (95% CI: 13 to 40) against influenza A(H1N1)pdm09, 68% (95% CI: 59 to 76) against B/Victoria, and 30% (95% CI: 9 to 47) against A(H3N2). Statistically significant protection against any influenza was found for all age groups except adults aged 50-64 years. Lack of protection in this age group was specific to influenza A-associated illness. We observed differences in VE by birth cohort and A(H1N1)pdm09 virus genetic subclade. Vaccination reduced outpatient medically attended influenza overall by 41% and provided protection overall against circulating influenza A and B viruses. Serologic studies would help inform differences observed by age groups.