Volume 18, Number 11—November 2012
Seroprevalence of Influenza A(H1N1)pdm09 Virus Antibody, England, 2010 and 2011
The intense influenza activity in England during the 2010–11 winter resulted from a combination of factors. Population-based seroepidemiology confirms that the third wave of influenza A(H1N1)pdm09 virus circulation was associated with a shift in age groups affected, with the highest rate of infection in young adults.
Seroepidemiologic data collected in England during the first 2 influenza pandemic waves suggested that another wave of infection with influenza A(H1N1)pdm09 virus was unlikely during 2010–11 (1). However, a substantial third wave occurred that affected persons in older age groups (2). Severity indicators suggested a higher level of illness and death, with increased cases in critical care and deaths. We conducted further seroepidemiologic study in England during 2010–11 to identify possible reasons for these observations.
This observational study used anonymized, residual serum samples from routine microbiological testing. Patient age and sex, date of sample collection, and source laboratory information were available (3).
Samples were from patients 0–99 years of age, of whom 53% were female. Samples were grouped according to collection date: pre–first wave (before April 2009 [1,403 samples]) and post–first wave (August–October 2009 [3,091 samples]); post–second wave (January–April 2010 [2,225 samples]); and pre–third wave (June–October 2010 [1,782 samples]) and post–third wave (February–April 2011 [1,257 samples]) (Figure 1). Availability of samples by region and patient age was not consistent. With the objective of measuring age-dependent incidence, we prioritized serum samples by patient age. Samples were spread across 7 age groups (<5, 5–14, 15–24, 25–44, 45–64, 65–74, and >75 years) and came from the 9 regions of England (East, East Midlands, London, North East, North West, South East, South West, West Midlands, and Yorkshire and Humber).
Viruses were characterized and sequenced as described (4). All samples were tested by hemagglutination-inhibition (HI) assay; samples with sufficient material also were tested by microneutralization assay according to standard methods (1). Samples with titers >32 or >40 by HI or microneutralization assay, respectively, were considered seropositive.
We determined antibody persistence by comparing antibody levels in the post–second wave panel with those of the pre–third wave panel on a subset of samples from 3 regions (North East, North West, and South West) where samples were available for both time points. Results were assessed with 95% confidence intervals. The full analysis of the seroprevalence preceding the 2010–11 season is detailed elsewhere (1).
In samples from all persons except those in the youngest age group (<5 years), antibody declined from the end of the 2009–10 winter season (post–second wave) to before the onset of the 2010–11 season (pre–third wave). This decline was limited (<10% reduction by HI and microneutralization assays in persons 5–74 years of age), with the largest reduction in the >75-year group (−15% and −20% by HI and microneutralization assays, respectively). In children <5 years, antibody levels increased (15% and 10% by HI and nicroneutralization assays, respectively) during the same time period (Table 1, Table 2; Figure 2).
We assessed changes in antibody levels during the 2010–11 season using data from all 5 available regions (East, North East, North West, South West, and Yorkshire and Humber) (Table 1, Table 2; Technical Appendix Table [PDF - 155 KB - 3 pages]). For all age groups, HI and microneutralization assays demonstrated similar trends, although the increase by microneutralization assay in elderly persons was lower than by HI assay (48% vs. 28% increase). We found no evidence for association of titer with sex or region.
Children in the 2 youngest groups (<14 years) had the highest titers overall and highest percentage of seropositive samples (Table 1, Table 2; Figure 2; Technical Appendix Table [PDF - 155 KB - 3 pages]). The highest increases in seroprevalence during the third wave were observed in the oldest age group (>75 years, from 17% to 65% seropositive by HI assay), followed by young adults (15–44 years, from 33% to 66% seropositive by HI assay) (Technical Appendix Figure [PDF - 155 KB - 3 pages]).
Clinical surveillance data obtained during the course of acute illness (2) and seroepidemiology through population sampling are consistent and together point toward a shift in the age range for infection with A(H1N1)pdm09 in the first season after the 2009 pandemic. This finding is similar to those in earlier pandemics (5) and other countries (6). Historical data, including from 1918, suggest that the initial impact in children is followed by a dramatic shift in age distribution of infected persons, with the probability of infection in adults exceeding those of children until the age distribution returns to the normal seasonal pattern (5,7). This adaptation process may take 3–10 years (7).
The rates of decline in antibody to A(H1N1)pdm09 from the 2009–10 to the 2010–11 winters are similar to historic data (8) and A(H1N1)pdm09 vaccine trials (9,10). The implications of such reduction are uncertain. The seroprevalence data suggested susceptibility in young adults pre–third wave, but not in children who were targeted by an extended vaccination program in the United Kingdom from January 2010. Up to 30% of children <5 years were vaccinated (11).
During the 2010–11 season, antibody was acquired primarily by young and old adults. The largest increase in antibody levels after the 2010–11 winter occurred in persons >75 years of age. Clinical surveillance data suggests that elderly persons (>65 years of age) were relatively spared from infection with A(H1N1)pdm09 virus (12). We propose that the increase resulted primarily from seasonal influenza vaccination in 2010–11 with vaccine uptake of 72.8% (13). In young adults (15–44 years), we believe that acquisition of antibody occurred as susceptible persons became infected during the winter. Children were relatively spared from infection with A(H1N1)pdm09 during winter 2010–11; their high rate of infection in the 2 previous pandemic waves, together with vaccination, left a limited number of susceptible persons (Figure 2).
Our study design—a retrospective, periodic, cross-sectional collection—has certain limitations. We analyzed similar but not identical groups and persons at different time points. For each sample, only limited information was available. Without information about vaccination status or influenza exposure history during the season, our interpretation of antibody levels and their changes has to be taken with caution. However, in this descriptive analysis we also used supportive evidence from UK influenza surveillance programs and take into account the date of vaccination timing and uptake, which strengthens our interpretation of the serologic data.
The collections for each sample set were distributed over time periods of up to 21 weeks, during which antibody levels would have changed, depending on the combined effects of seroconversion, antibody waning and availability of vaccination. A novel likelihood-based approach, described previously has therefore been developed to overcome some of the limitations of the conventional statistical method (1).
We found no evidence of substantial antigenic drift in circulating viruses that could affect seroepidemiology results (Technical Appendix Table [PDF - 155 KB - 3 pages]). We conclude that the intense A(H1N1)pdm09 virus activity in the England during the 2010–11 winter must have resulted from a combination of factors.
The change in age distribution of infection is likely to have caused increased severity, resulting from a larger number of patients with underlying concurrent conditions (12) or from age-dependent changes in pathology. Defining antibody correlates of protection becomes more complex with rising patient age as other immune mechanisms increasingly contribute to protection, e.g., CD4+ T cells, as demonstrated in human challenge experiments (14). Moreover, a murine model identified the role of age in susceptibility to pathogenesis and transmission of influenza virus infection (15). These observations might help to provide some mechanistic insights for the shift in age distribution of infection and severity in the season after the 2009 pandemic. Genetic drift in circulating virus over time affecting human airway adaptation and varying climatic conditions during different pandemic waves also should be investigated.
Dr Hoschler is Advanced Clinical Scientist at the Respiratory Virus Unit, Microbiology Services–Colindale, Health Protection Agency, UK. Her research is focused on influenza serology, including the investigation of natural and vaccine responses, influenza seroepidemiology and development of new diagnostic serologic assays.
We thank the Health Protection Agency Regional Microbiology Network and National Health Service laboratories that collect samples for the Health Protection Agency seroepidemiology program. We are grateful for the technical support provided by Janice Baldevarona, Surita Gangar, Paola Barbero, Dipa Lakhman, Ray Borrow, Kevin Potts, and Sam Tomes.
This study was funded by the National Institute for Health Research Health Technology Assessment Programme and the Department of Health.
- Hardelid P, Andrews NJ, Hoschler K, Stanford E, Baguelin M, Waight PA, Assessment of baseline age-specific antibody prevalence and incidence of infection to novel influenza A/H1N1 2009. Health Technol Assess. 2010;14:115–92.
- Presanis AM, Pebody RG, Paterson BJ, Tom BD, Birrell PJ, Charlett A, Changes in severity of 2009 pandemic A/H1N1 influenza in England: a Bayesian evidence synthesis. BMJ. 2011;343:d5408.
- Health Protection Agency. Seroepidemiology Programme. London [cited 2012 May 14]. http://www.hpa.org.uk/Topics/InfectiousDiseases/InfectionsAZ/SeroepidemiologyProgramme/
- Galiano M, Agapow PM, Thompson C, Platt S, Underwood A, Ellis J, Evolutionary pathways of the pandemic influenza A (H1N1) 2009 in the UK. PLoS ONE. 2011;6:e23779.
- Simonsen L, Clarke MJ, Schonberger LB, Arden NH, Cox NJ, Fukuda K. Pandemic versus epidemic influenza mortality: a pattern of changing age distribution. J Infect Dis. 1998;178:53–60.
- Viasus D, Cordero E, Rodriguez-Bano J, Oteo JA, Fernandez-Navarro A, Ortega L, Changes in epidemiology, clinical features and severity of influenza A (H1N1) 2009 pneumonia in the first post-pandemic influenza season. Clin Microbiol Infect. 2012;18:E55–62.
- Saglanmak N, Andreasen V, Simonsen L, Molbak K, Miller MA, Viboud C. Gradual changes in the age distribution of excess deaths in the years following the 1918 influenza pandemic in Copenhagen: using epidemiological evidence to detect antigenic drift. Vaccine. 2011;29(Suppl 2):B42–8.
- Davies JR, Grilli EA, Smith AJ. Infection with influenza A H1N1. 2. The effect of past experience on natural challenge. J Hyg (Lond). 1986;96:345–52.
- Nicholson KG, Abrams KR, Batham S, Clark TW, Hoschler K, Lim WS, A randomised, partially observer blind, multicentre, head-to-head comparison of a two-dose regimen of Baxter and GlaxoSmithKline H1N1 pandemic vaccines, administered 21 days apart. Health Technol Assess. 2010;14:193–334.
- Walker WT, de Whalley P, Andrews N, Oeser C, Casey M, Michaelis L, H1N1 antibody persistence 1 year after immunization with an adjuvanted or whole-virion pandemic vaccine and immunogenicity and reactogenicity of subsequent seasonal influenza vaccine: a multicenter follow-on study. Clin Infect Dis. 2012;54:661–9.
- Health Protection Agency. Pandemic H1N1 (swine) influenza vaccine uptake amongst patient groups in primary care in England 2009/10 [cited 2012 May 14]. http://www.dh.gov.uk/prod_consum_dh/groups/dh_digitalassets/@dh/@en/@ps/documents/digitalasset/dh_121014.pdf
- Health Protection Agency. Surveillance of influenza and other respiratory viruses in the UK: 2010–2011 report [cited 2012 May 14]. http://www.hpa.org.uk/webc/HPAwebFile/HPAweb_C/1296687414154
- Health Protection Agency. Seasonal influenza vaccine uptake amongst GP patient groups in England. Winter season 2010–11 [cited 2012 May 14]. http://www.dh.gov.uk/prod_consum_dh/groups/dh_digitalassets/documents/digitalasset/dh_129856.pdf
- Wilkinson TM, Li CK, Chui CS, Huang AK, Perkins M, Liebner JC, Preexisting influenza-specific CD4(+) T cells correlate with disease protection against influenza challenge in humans. Nat Med. 2012;18:274–80.
- Sun S, Zhao G, Xiao W, Hu J, Guo Y, Yu H, Age-related sensitivity and pathological differences in infections by 2009 pandemic influenza A (H1N1) virus. Virol J. 2011;8:52.
Suggested citation for this article: Hoschler K, Thompson C, Andrews N, Galiano M, Pebody R, Ellis J, et al. Seroprevalence of influenza A(H1N1)pdm09 virus antibody, England, 2010 and 2011. Emerg Infect Dis [Internet]. 2012 Nov [date cited]. http://dx.doi.org/10.3201/eid1811.120720
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