Skip directly to search Skip directly to A to Z list Skip directly to page options Skip directly to site content

Volume 18, Number 11—November 2012


Seroprevalence of Pandemic Influenza Viruses, New York, New York, USA, 2004

On This Page


Technical Appendicies

Suggested citation for this article

To the Editor: Exposures to influenza viruses can lead to immune responses that substantially affect susceptibility to infection with related viruses. Characterization of preexisting immunity within a population can inform public health, as highlighted during the influenza A(H1N1)pdm09 virus pandemic, when surveillance data demonstrated that older persons (>65 years old) were less likely than younger persons to have influenza (1). Seroprevalence studies of prepandemic samples show that older persons had preexisting antibody responses to A(H1N1)pdm09 virus, presumably because of prior exposure to related strains (2). The A(H1N1)pdm09 virus possesses hemagglutinin and neuraminidase genes derived from classical swine influenza virus (3).

Epidemiologic and molecular data indicate that prior exposure to early twentieth century H1N1 viruses conferred immunity to A(H1N1)pdm09 virus. Human antibodies that neutralize A(H1N1)pdm09 virus and H1N1 subtype viruses from earlier in the twentieth century have been characterized, and animal studies have demonstrated that antibodies to the earlier H1N1 subtype viruses cross-neutralize A(H1N1)pdm09 virus and protect from virus challenge (2,46). Prior exposure to antigenically related viruses can explain the relationship between age and susceptibility to infection.


Thumbnail of Seroprevalence of cross-reactive antibodies to the 1918, 1957, 1968, and 2009 pandemic influenza viruses among persons >23 years of age, New York, New York, 2004. LOESS (locally weighted scatterplot smoothing) curves represent the estimated prevalence of hemagglutination-inhibition antibody titers of >40 (positive titers) by year of birth.

Figure. Seroprevalence of cross-reactive antibodies to the 1918, 1957, 1968, and 2009 pandemic influenza viruses among persons >23 years of age, New York, New York, 2004. LOESS (locally weighted scatterplot smoothing) curves...

To determine the seroprevalence of preexisting hemagglutinin inhibition (HAI) antibody titers to influenza strains with pandemic potential, we tested serum samples for antibodies to A(H1N1)pdm09 virus and the 1918, 1957, and 1968 pandemic viruses. The samples had been collected in 2004 from a representative sample of adults in New York City (NYC), USA, as part of the NYC Health and Nutrition Examination Survey (Technical Appendix [PDF - 315 KB - 7 pages]). For the 1918 and A(H1N1)pdm09 viruses, the highest prevalence of HAI titers >40 was among persons born before 1940 (>65 years old in 2004), although younger adults also had antibodies. Antibody prevalence to the 1957 H2N2 subtype virus was highest among persons born during 1942–1961, and >70% in persons born before 1971 had antibody to the 1968 H3N2 subtype virus (Figure). For all pandemic viruses, there was no significant difference in seroprevalence by sex or by US birth and only minor differences by race/ethnicity (Technical Appendix Table 1 [PDF - 315 KB - 7 pages]).

We examined A(H1N1)pdm09 virus seroprevalence by the age of persons tested and by antibody titer. The mean age for persons with no serologic evidence of prior exposure (titer <20) was 50 years, compared with 72 years for those with titers of 20–40 and 80 years for those with titers >40 (Technical Appendix Table 2 [PDF - 315 KB - 7 pages]). In a multivariate logistic regression model, presence of antibody to the 1918 H1N1 subtype virus was strongly associated with antibody to A(H1N1)pdm09 virus (Technical Appendix Table 3 [PDF - 315 KB - 7 pages]). No demographic factor was independently associated with positivity to A(H1N1)pdm09 virus. By using a nonlinear regression model for the probability of A(H1N1)pdm09 antibody prevalence compared with birth year, we found the model that best fit the age-stratified seroprevalence data inflected near 1927 (Technical Appendix Figure [PDF - 315 KB - 7 pages]), indicating that persons born before 1927 were most reliably protected.

Our findings show that the prevalence of pandemic influenza virus antibody in a representative population-based 2004 sample of NYC residents correlated with birth year and year(s) of circulating virus. These data reveal the immunologic background during the emergence of A(H1N1)pdm09 virus in NYC beginning in late April 2009 (7) and help explain why fewer cases of A(H1N1)pdm09 infection were detected among older persons than younger persons, supporting the conclusion that the difference was a result of, at least in part, antibodies elicited by prior H1N1 subtype infection in older persons.

Viruses antigenically resembling the 1918 pandemic strain circulated among humans earlier in the twentieth century; cross-reactivity with antibodies to those viruses likely provided protection against the 1918 virus. Most (2,4), but not all (8), previous A(H1N1)pdm09 virus seroprevalence studies demonstrated an increase in immunity with age. In our study, more persons born before than after 1927 (i.e., persons >82 vs. those 65–82 years of age in 2009) had HAI assay results positive for A(H1N1)pdm09 virus. Protection among persons 65–82 years old during the 2009 pandemic may be explained by the presence of preexisting immunity not measured by standard HAI tests (e.g., antibodies that target the hemagglutinin stalk) or by T-cell responses (9). More positive test results were recorded with the 1918 than the A(H1N1)pdm09 virus; this finding is consistent with the model in which preexisting immunity to A(H1N1)pdm09 virus was derived from exposure to the 1918 pandemic strain or to antigenically related strains that evolved since then (10). The 1918 and 2009 strains used in testing may have exhibited different sensitivities in HAI assays. Immunity in older populations is not surprising and was seen in the 1918, 1957, and 1968 pandemics, during which newly introduced pandemic viruses were more likely to cause clinical illness in younger persons, presumably because prior exposure to similar viruses resulted in cross-reactive antibodies (11).

Study limitations include a relatively small sample size and a lack of history regarding influenza virus infection or vaccination. Nevertheless, the ability to evaluate seroreactivity in a representative sample of adults helps validate and reinforce previously published findings on H1N1 subtype viruses and clarifies levels of immunity to H2N2 and H3N2 subtype viruses.

Isaac B. Weisfuse, Tshidi Tsibane, Kevin J. KontyComments to Author , Joseph R. Egger1, Elizabeth Needham Waddell, Saad Rahmat, Emily Harris, Donald R. Olson, and Christopher F. Basler
Author affiliations: New York City Department of Health and Mental Hygiene, New York, New York, USA (I.B. Weisfuse, K.J. Konty, J.R. Egger, E.N. Wadell, D.R. Olson); Mount Sinai School of Medicine, New York (T. Tsibane, S. Rahmat, E. Harris, C.F. Basler); and International Society for Disease Surveillance, New York, (D.R. Olson)


This study was supported, in part, by National Institutes of Health grants AI072258 and U54 AI057158 (the Northeast Biodefense Center-Lipkin grant) to C.F.B.


  1. Jhung MA, Swerdlow D, Olsen SJ, Jernigan D, Biggerstaff M, Kamimoto L, Epidemiology of 2009 pandemic influenza A (H1N1) in the United States. Clin Infect Dis. 2011;52(Suppl 1):S1326. DOIPubMed
  2. Itoh Y, Shinya K, Kiso M, Watanabe T, Sakoda Y, Hatta M, In vitro and in vivo characterization of new swine-origin H1N1 influenza viruses. Nature. 2009;460:10215.PubMed
  3. Novel Swine-Origin Influenza A. (H1N1) Virus Investigation Team. Emergence of a novel swine-origin influenza A (H1N1) virus in humans. N Engl J Med. 2009;360:260515. DOIPubMed
  4. Hancock K, Veguilla V, Lu X, Zhong W, Butler EN, Sun H, Cross-reactive antibody responses to the 2009 pandemic H1N1 influenza virus. N Engl J Med. 2009;361:194552. DOIPubMed
  5. McCullers JA, Van De Velde LA, Allison KJ, Branum KC, Webby RJ, Flynn PM. Recipients of vaccine against the 1976 “swine flu” have enhanced neutralization responses to the 2009 novel H1N1 influenza virus. Clin Infect Dis. 2010;50:148792. DOIPubMed
  6. Garten RJ, Davis CT, Russell CA, Shu B, Lindstrom S, Balish A, Antigenic and genetic characteristics of swine-origin 2009 A(H1N1) influenza viruses circulating in humans. Science. 2009;325:197201. DOIPubMed
  7. Lessler J, Reich NG, Cummings DAT; New York City Department of Health and Mental Hygiene Swine Flu Investigation Team. Outbreak of 2009 pandemic influenza A (H1N1) at a New York City school. N Engl J Med. 2009;361:262836. DOIPubMed
  8. Chen H, Wang Y, Liu W, Zhang J, Dong B, Fan X, Serologic survey of pandemic (H1N1) 2009 virus, Guangxi Province, China. Emerg Infect Dis. 2009;15:184950. DOIPubMed
  9. Wrammert J, Koutsonanos D, Li GM, Edupuganti S, Sui J, Morrissey M, Broadly cross-reactive antibodies dominate the human B cell response against 2009 pandemic H1N1 influenza virus infection. J Exp Med. 2011;208:18193. DOIPubMed
  10. Zimmer SM, Crevar CJ, Carter DM, Stark JH, Giles BM, Zimmerman RK, Seroprevalence following the second wave of pandemic 2009 H1N1 influenza in Pittsburgh, PA, USA. PLoS ONE. 2010;5:e11601. DOIPubMed
  11. Dowdle WR. Influenza A virus recycling revisited. Bull World Health Organ. 1999;77:8208.PubMed


Technical Appendix

Suggested citation for this article: Weisfuse IB, Tsibane T, Konty KJ, Egger JR, Waddell EN, Rahmat S, et al. Seroprevalence of pandemic influenza viruses, New York, New York, USA, 2004 [letter]. Emerg Infect Dis [Internet]. 2012 Nov [date cited].

DOI: 10.3201/eid1811.120156

1Current affiliation: SciMetrika, LLC, Research Triangle Park, North Carolina, USA.

Related Links

Table of Contents – Volume 18, Number 11—November 2012

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Kevin J. Konty, New York City Department of Health and Mental Hygiene, Gotham Center, 42-09 28th St, Long Island City, New York 10471, USA

character(s) remaining.

Comment submitted successfully, thank you for your feedback.

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.