Seasonal Vaccine against Pandemic (H1N1) 2009 | CDC EID

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Volume 17, Number 7–July 2011
Research
Effectiveness of Seasonal Influenza Vaccine against Pandemic (H1N1) 2009 Virus, Australia, 2010
James E. Fielding, Kristina A. Grant, Katherine Garcia, and Heath A. Kelly Author affiliations: Victorian Infectious Diseases Reference Laboratory, North Melbourne, Victoria, Australia (J.E. Fielding, K.A. Grant, K. Garcia, H.A. Kelly); and The Australian National University, Canberra, Australian Capital Territory, Australia (J.E. Fielding)

Suggested citation for this article

Abstract
To estimate effectiveness of seasonal trivalent and monovalent influenza vaccines against pandemic influenza A (H1N1) 2009 virus, we conducted a test-negative case–control study in Victoria, Australia, in 2010. Patients seen for influenza-like illness by general practitioners in a sentinel surveillance network during 2010 were tested for influenza; vaccination status was recorded. Case-patients had positive PCRs for pandemic (H1N1) 2009 virus, and controls had negative influenza test results. Of 319 eligible patients, test results for 139 (44%) were pandemic (H1N1) 2009 virus positive. Adjusted effectiveness of seasonal vaccine against pandemic (H1N1) 2009 virus was 79% (95% confidence interval 33%–93%); effectiveness of monovalent vaccine was 47% and not statistically significant. Vaccine effectiveness was higher among adults. Despite some limitations, this study indicates that the first seasonal trivalent influenza vaccine to include the pandemic (H1N1) 2009 virus strain provided significant protection against laboratory-confirmed pandemic (H1N1) 2009 infection.


After the emergence and rapid global spread of pandemic influenza A (H1N1) 2009 virus, development of a pandemic (H1N1) 2009–specific vaccine began (1). A candidate reassortant vaccine virus, derived from the A/California/7/2009 (H1N1)v virus as recommended by the World Health Organization, was used to produce a monovalent, unadjuvanted, inactivated, split-virus vaccine for Australia (2,3). The national monovalent pandemic (H1N1) 2009 vaccination program in Australia ran from September 30, 2009, through December 31, 2010, and vaccination was publicly funded for all persons in Australia >6 months of age (4,5).

In September 2009, the World Health Organization recommended that trivalent influenza vaccines for use in the 2010 influenza season (Southern Hemisphere winter) contain A/California/7/2009 (H1N1)–like virus, A/Perth/16/2009 (H3N2)–like virus, and B/Brisbane/60/2008 (of the B/Victoria/2/87 lineage) virus (6). Since March 2010, the Australian Government has provided free seasonal influenza vaccination to all Australia residents >65 years of age, all Aboriginal and Torres Strait Islander persons >50 years, all Aboriginal and Torres Strait Islander persons 15–49 years with medical risk factors, persons >6 months with conditions that predispose them to severe influenza, and pregnant women (7). Influenza vaccination is also recommended, but not funded, for persons who might transmit influenza to those at high risk for complications from influenza, persons who provide essential services, travelers, and anyone >6 months of age for whom reducing the likelihood of becoming ill with influenza is desired. Individual industries are also advised to consider the benefits of offering influenza vaccine in the workplace (8). Because pandemic (H1N1) 2009 was expected to be the dominant strain in 2010, the monovalent vaccine continued to be used despite the availability of the seasonal vaccine, particularly by persons who were not eligible for funded vaccine (M. Batchelor, pers. comm.). However, in 2010, there were no published data on the relative use of monovalent and seasonal vaccines at that time.

The need for rapid implementation of programs results in initial studies using immunogenicity, rather than efficacy, to assess performance of influenza vaccines. After 1 dose of monovalent pandemic (H1N1) 2009 vaccine containing 15 μg hemagglutinin without adjuvant, seroprotection was estimated to be 94%–97% in working-age adults (3,9,10) and 75% in children (10). Observational studies provide a practical way to calculate vaccine effectiveness under field conditions (11,12). Effectiveness of monovalent pandemic (H1N1) 2009 was estimated to be 72%–97% by 3 studies in general practice and community-based settings in Europe (13–15), 90% in a hospital-based study in Spain (16), and 100% in a community-based study of children in Canada (17). These studies were conducted in populations for which the respective local or national pandemic vaccination program primarily used vaccine without adjuvant.
We assessed effectiveness of the 2010 seasonal influenza vaccine against laboratory-confirmed pandemic (H1N1) 2009 influenza infection in Victoria, Australia. Data came from an established test-negative case–control study in a general practitioner sentinel surveillance network (18,19).

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Seasonal Vaccine against Pandemic (H1N1) 2009 CDC EID


Suggested Citation for this Article
Fielding JE, Grant KA, Garcia K, Kelly HA. Effectiveness of seasonal influenza vaccine against pandemic (H1N1) 2009 virus, Australia, 2010. Emerg Infect Dis [serial on the Internet]. 2011 Jul [date cited]. http://www.cdc.gov/EID/content/17/7/1181.htm
DOI: 10.3201/eid1707.101959

Comments to the Authors
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James E. Fielding, 10 Wreckyn St, North Melbourne, Victoria 3051, Australia; email: james.fielding@mh.org.au