Prevention and Control of Seasonal Influenza with Vaccines: Recommendations of the Advisory Committee on Immunization Practices - United States, 2025-26 Influenza Season.

IF 17.3 1区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Lisa A Grohskopf, Lenee H Blanton, Jill M Ferdinands, Carrie Reed, Vivien G Dugan, Demetre C Daskalakis
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Abstract

This report updates the 2024-25 recommendations of the Advisory Committee on Immunization Practices (ACIP) concerning the use of seasonal influenza vaccines in the United States. Routine annual influenza vaccination is recommended for all persons aged ≥6 months who do not have a contraindication to vaccination. Multiple formulations of the trivalent inactivated influenza vaccines (IIV3s), trivalent recombinant influenza vaccine (RIV3), and trivalent live attenuated influenza vaccine (LAIV3) are expected to be available for the 2025-26 influenza season. Updates for the 2025-26 season include 1) antigenic composition of 2025-26 U.S. seasonal influenza vaccines, 2) Food and Drug Administration (FDA) approval of FluMist (LAIV3) for self-administration or caregiver administration, 3) FDA approval of a change in age indication for Flublok (RIV3) from ≥18 years to ≥9 years, and 4) a new ACIP recommendation that children aged ≤18 years, pregnant women, and all adults receive seasonal influenza vaccines only in single-dose formulations that are free of thimerosal as a preservative. A comprehensive summary of recommendations, including those discussed in this report, as well as previous recommendations concerning topics not addressed in this report and that remain unchanged for the 2025-26 season, is available at Influenza | ACIP Recommendations for Vaccination. Additional background information also is available at Prevention and Control of Seasonal Influenza with Vaccines.

用疫苗预防和控制季节性流感:免疫实践咨询委员会的建议——美国,2025-26年流感季节
本报告更新了免疫实践咨询委员会(ACIP)关于在美国使用季节性流感疫苗的2024-25年建议。建议所有年龄≥6个月且无接种禁忌症的人每年常规接种流感疫苗。预计2025-26年流感季节将有多种配方的三价灭活疫苗(IIV3s)、三价重组流感疫苗(RIV3)和三价减毒活疫苗(LAIV3)。2025-26年流感季的最新进展包括:1)2025-26年美国季节性流感疫苗的抗原组成;2)美国食品和药物管理局(FDA)批准fluumist (LAIV3)用于自我给药或护理人员给药;3)FDA批准Flublok (RIV3)的适应症从≥18岁更改为≥9岁;4)新的ACIP建议≤18岁的儿童、孕妇、所有成年人只接种不含硫柳汞作为防腐剂的单剂量季节性流感疫苗。建议的综合摘要,包括本报告中讨论的建议,以及以前关于本报告未涉及的主题的建议,并且在2025-26季节保持不变,可在流感| ACIP疫苗接种建议中获得。有关更多背景资料,请参阅“用疫苗预防及控制季节性流感”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
MMWR. Morbidity and mortality weekly report
MMWR. Morbidity and mortality weekly report PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH -
CiteScore
65.40
自引率
0.90%
发文量
309
期刊介绍: The Morbidity and Mortality Weekly Report (MMWR ) series is prepared by the Centers for Disease Control and Prevention (CDC). Often called “the voice of CDC,” the MMWR series is the agency’s primary vehicle for scientific publication of timely, reliable, authoritative, accurate, objective, and useful public health information and recommendations. MMWR readership predominantly consists of physicians, nurses, public health practitioners, epidemiologists and other scientists, researchers, educators, and laboratorians.
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