Among adults ≥18 years, outpatient VE was 36%–54%, and hospitalization VE 41%–55%.³ Adults 18–64 years had outpatient VE 37–56% and hospitalization VE 48–51%; adults ≥65 years had outpatient VE 18–51% (one estimate non-significant) and hospitalization VE 38–57%.⁴ Vaccination coverage among test-negative controls was generally 20–40% in children and about one third in adults, reflecting continued room to improve uptake. Nearly all sequenced viruses remained well matched to vaccine strains, including clade 2a.3a.1 A(H3N2) and clades 5a.2a and 5a.2a.1 A(H1N1)pdm09.⁴
What You Need to Know
The 2024–2025 influenza season saw the highest hospitalization rate in over a decade, yet only about one-third of hospitalized patients were vaccinated, and antiviral use in children lagged. High illness burden was driven by incidence rather than viral virulence, underscoring persistent gaps in both vaccination uptake and timely treatment.
For the new season, CDC introduced universal thimerosal-free single-dose formulations, expanded access to FluMist (including self- or caregiver administration), and broadened the FluBlok age indication. These changes—along with stable supply—are intended to reduce barriers and improve uptake across age groups.
Initial FluView data show H3N2 accounting for over 80% of subtyped cases, low but increasing outpatient illness, and strong antigenic match for most circulating viruses (with partial match to H3N2). With more than 124 million doses already distributed, experts emphasize continued vaccination and early antiviral treatment as key tools as the season progresses.
CDC’s 2025–2026 Recommendations: Trivalent, Thimerosal-Free Single Doses
Against this backdrop, CDC issued its final 2025–2026 guidance on November 17, 2025, reaffirming annual influenza vaccination for all persons ≥6 months and highlighting several changes intended to simplify delivery and reduce barriers. All US vaccines for 2025–2026 are trivalent, targeting A(H1N1)pdm09, A(H3N2), and B/Victoria-lineage viruses.² Egg-based vaccines contain A/Victoria/4897/2022 (H1N1)pdm09-like, A/Croatia/10136RV/2023 (H3N2)-like, and B/Austria/1359417/2021 (B/Victoria)-like strains; cell-based and recombinant vaccines contain A/Wisconsin/67/2022 (H1N1)pdm09-like, A/District of Columbia/27/2023 (H3N2)-like, and the same B/Victoria component.²
CDC now recommends exclusive use of single-dose, thimerosal-free formulations for children, pregnant patients, and adults.² FluMist is newly approved for self- or caregiver administration, and FluBlok’s age indication has expanded to ≥9 years. Manufacturers expect up to 154 million doses this season, with no anticipated supply constraints. Vaccination remains widely available at no cost through insurance coverage, community clinics, HRSA-supported centers, and the Vaccines for Children program.²
Early 2025–2026 Surveillance: H3N2 Dominant but Activity Still Low
CDC’s Week 47 FluView report provides the first detailed snapshot of the new season. Nationally, 5% of respiratory specimens tested by clinical labs were influenza positive, and 2.5% of outpatient visits were for respiratory illness, below the 3.1% baseline but rising.³ CDC estimates 1.1 million illnesses, 11,000 hospitalizations, and 450 deaths so far this season, with no pediatric deaths to date.³ More than 124 million doses of vaccine have been distributed.³
Among 305 subtyped influenza A specimens, 82.3% were A(H3N2) and 17.7% A(H1N1)pdm09; no A(H5) viruses were detected.³ Outpatient ILI and emergency department visits increased primarily among individuals 0–49 years.³ FluSurv-NET documented 905 hospitalizations from October 1 to November 22 (cumulative rate 2.6 per 100,000), with the highest rates in adults ≥65 years (7.5 per 100,000).³
Antigenic analyses of 589 viruses showed strong similarity to vaccine components for A(H1N1)pdm09 and B/Victoria, and partial match for A(H3N2), where 33.3% of viruses were well recognized by antisera to the updated vaccine component.³ Antiviral susceptibility remained highly favorable, with only one A(H1N1)pdm09 virus (0.2%) showing reduced inhibition to oseltamivir and one (0.2%) to baloxavir.³
Implications for Vaccination and Clinical Practice in 2025
Taken together, last season’s high burden, moderate VE, updated recommendations, and early-season trends reinforce a consistent message: vaccination remains the most effective strategy to reduce influenza morbidity and hospitalization, and timely antiviral treatment is essential for high-risk and hospitalized patients.²⁻⁴ Early data suggest persistent gaps in vaccination coverage among both hospitalized populations and test-negative controls, underscoring the importance of routine primary care, pharmacy-based vaccination, and strong clinician recommendations. As H3N2 continues to dominate, clinicians should remain alert to severe respiratory illness, monitor for zoonotic exposures in the context of H5 virus activity, and follow NFID, IDSA, and CDC updates as more data emerge through the core months of the 2025–2026 season.
References
1.O’Halloran A, Habeck JW, Gilmer M, et al. Influenza-Associated Hospitalizations During a High Severity Season — Influenza Hospitalization Surveillance Network, United States, 2024–25 Influenza Season. MMWR Morb Mortal Wkly Rep 2025;74:529–537. DOI: http://dx.doi.org/10.15585/mmwr.mm7434a1
3.CDC. Weekly US Influenza Surveillance Report: Key Updates for Week 47, ending November 22, 2025. December 1, 2025. Accessed December 2, 2025. https://www.cdc.gov/fluview/surveillance/2025-week-47.html
4.Frutos AM, Cleary S, Reeves EL, et al. Interim Estimates of 2024–2025 Seasonal Influenza Vaccine Effectiveness — Four Vaccine Effectiveness Networks, United States, October 2024–February 2025. MMWR Morb Mortal Wkly Rep 2025;74:83–90. DOI: http://dx.doi.org/10.15585/mmwr.mm7406a