Spread of Antigenically Drifted Influenza A(H3N2) Viruses and Vaccine Effectiveness in the United States During the 2018–2019 Season

Author:

Flannery Brendan1,Kondor Rebecca J Garten1,Chung Jessie R1,Gaglani Manjusha2,Reis Michael2,Zimmerman Richard K3,Nowalk Mary Patricia3,Jackson Michael L4,Jackson Lisa A4,Monto Arnold S5,Martin Emily T5,Belongia Edward A6,McLean Huong Q6,Kim Sara S7,Blanton Lenee1,Kniss Krista1,Budd Alicia P1,Brammer Lynnette1,Stark Thomas J1,Barnes John R1,Wentworth David E1,Fry Alicia M1,Patel Manish1

Affiliation:

1. Influenza Division, Centers for Disease Control and Prevention, Atlanta, Georgia

2. Baylor Scott & White Health, Texas A&M University College of Medicine, Temple, Texas

3. University of Pittsburgh Schools of Health Sciences and University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania

4. Kaiser Permanente Washington Health Research Institute, Seattle, Washington

5. University of Michigan School of Public Health, Ann Arbor, Michigan

6. Marshfield Clinic Research Institute, Marshfield, Wisconsin

7. Oak Ridge Institute for Science and Education Fellowship Program, Oak Ridge, Tennessee

Abstract

Abstract Background Increased illness due to antigenically drifted A(H3N2) clade 3C.3a influenza viruses prompted concerns about vaccine effectiveness (VE) and vaccine strain selection. We used US virologic surveillance and US Influenza Vaccine Effectiveness (Flu VE) Network data to evaluate consequences of this clade. Methods Distribution of influenza viruses was described using virologic surveillance data. The Flu VE Network enrolled ambulatory care patients aged ≥6 months with acute respiratory illness at 5 sites. Respiratory specimens were tested for influenza by means of reverse-transcriptase polymerase chain reaction and were sequenced. Using a test-negative design, we estimated VE, comparing the odds of influenza among vaccinated versus unvaccinated participants. Results During the 2018–2019 influenza season, A(H3N2) clade 3C.3a viruses caused an increasing proportion of influenza cases. Among 2763 Flu VE Network case patients, 1325 (48%) were infected with A(H1N1)pdm09 and 1350 (49%) with A(H3N2); clade 3C.3a accounted for 977 (93%) of 1054 sequenced A(H3N2) viruses. VE was 44% (95% confidence interval, 37%–51%) against A(H1N1)pdm09 and 9% (−4% to 20%) against A(H3N2); VE was 5% (−10% to 19%) against A(H3N2) clade 3C.3a viruses. Conclusions The predominance of A(H3N2) clade 3C.3a viruses during the latter part of the 2018–2019 season was associated with decreased VE, supporting the A(H3N2) vaccine component update for 2019–2020 northern hemisphere influenza vaccines.

Funder

Kaiser Permanent Washington Health Research Institute

Marshfield Clinic Research Institute

Baylor Scott & White Health

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

Reference23 articles.

1. Recommended composition of influenza virus vaccines for use in the 2019–2020 northern hemisphere influenza season;World Health Organization;Wkly Epidemiol Rec,2019

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