During the autumn wave of the pandemic influenza virus A/(H1N1) 2009 (pIV) the German population was offered an AS03-adjuvanted vaccine. The authors compared results of two methods calculating the effectiveness of the vaccine (VE). The test-negative case-control method used data from virologic surveillance including influenza-positive and negative patients. An innovative case-series methodology explored data from all nationally reported laboratory-confirmed influenza cases. The proportion of reported cases occurring in vaccinees during an assumed unprotected phase after vaccination was compared with that occurring in vaccinees during their assumed protected phase. The test-negative case-control method included 1,749 pIV cases and 2,087 influenza test-negative individuals of whom 6 (0.3%) and 36 (1.7%), respectively, were vaccinated. The case series method included data from 73,280 cases. VE in the two methods was 79% (95% confidence interval (CI) = 35–93%; P = 0.007) and 87% (95% CI = 78–92%; P<0.001) for individuals less than 14 years of age and 70% (95% CI = −45%–94%, P = 0.13) and 74% (95% CI = 64–82%; P<0.001) for individuals above the age of 14. Both methods yielded similar VE in both age groups; and VE for the younger age group seemed to be higher.
Citation: Uphoff H, an der Heiden M, Schweiger B, Campe H, Beier D, et al. (2011) Effectiveness of the AS03-Adjuvanted Vaccine against Pandemic Influenza Virus A/(H1N1) 2009 – A Comparison of Two Methods; Germany, 2009/10. PLoS ONE 6(7): e19932. doi:10.1371/journal.pone.0019932
Editor: Troy D. Randall, University of Rochester School of Medicine, United States of America
Received: November 4, 2010; Accepted: April 22, 2011; Published: July 18, 2011
Copyright: © 2011 Uphoff et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Phase 6 of the 2009 pandemic caused by the influenza virus A/(H1N1) 2009 (pIV) started with the announcement of the World Health Organization on June 11, 2009. For countries of the Northern hemisphere, including Germany, a vaccine became available after the autumn wave had already started. In Germany for the most part of the autumn wave, only one type of vaccine was available which was an egg-based vaccine containing 3.75 µg hemagglutinine as antigenic component and the adjuvant AS03.
Prior to the pandemic it was anticipated that a pandemic vaccine - even when adjuvanted - needs to be given twice to induce protective immunity . However, tests with the pandemic vaccine containing pIV antigen have shown that a single vaccine dose of 15 µg without adjuvant may be sufficient in participants between 3 and 77 years of age . Other studies suggested that a single dose of squalen-adjuvanted vaccine directed against pIV may induce sufficient levels of immunity in adults (using 3.75 µg hemagglutinine)  and even in children 6–36 months old (using 1.9 µg antigen) .
In Germany, the vaccine adjuvanted with the squalene AS03 became available to the population from week 44/2009 onwards. The German standing committee for vaccination recommended the vaccine for the entire population, prioritizing medical personnel, persons with chronic underlying conditions and pregnant women . While initially two doses were recommended for children up to 9 years and elderly persons, an updated statement recommended a single dose for all age groups .
Recently, Orenstein has compared several methods to estimate VE for influenza from observational data including the test-negative case-control method . To extend the repertoire of observational study types incorporating the fact that the vaccination campaign occurred concurrently with the epidemic wave we attempted to explore another method which has not been described previously and uses nationally reported cases of influenza only. The method is motivated by the self-controlled case series method that has been used in studies on vaccine safety .
The objective of this paper is to assess VE of the AS03-adjuvanted pIV vaccine using two methods: first, the test-negative case control method; second, a novel form of a case-series method.
Materials and Methods
Laboratory test-negative case-control method
For this evaluation only patient samples taken with diagnostic intent were analysed. Due to German standards, ethics approval and informed consent was not necessary.
We used the test-negative case-control study design similar to that described in the ECDC technical document (2009) . We obtained virologic surveillance data from the National Reference Center for Influenza at the Robert Koch-Institute (RKI), and the State Laboratories of Mecklenburg-Western-Pommerania (Rostock), Saxonia-Anhalt (Magdeburg), Bavaria (Oberschleissheim) and Saxonia (Dresden), Germany. Samples were provided by physicians who swabbed patients with influenza-like illness (ILI). Samples were accompanied by a patient-based questionnaire with information on age, sex, state of residence, date of symptom onset, symptoms, underlying disease (cardiovascular, respiratory, diabetes) and dates of vaccination against seasonal and pandemic influenza, if any. Cases were confirmed by reverse-transcriptase polymerase chain reaction (RT-PCR), controls were RT-PCR negative. Hospitalized ILI patients and test-negative patients where swabs were taken more than four days after disease onset were excluded. Because vaccination against pandemic influenza virus started in week 44/2009, we restricted data analysis to patients with illness onset between week 44/2009 and 07/2010. For seasonal and pandemic A/H1N1 2009 influenza vaccine it has been shown that 90% and 79% of vaccinees, respectively, had protective antibody titres two weeks after vaccination , . We defined therefore patients as vaccinated when more than two weeks had passed after the date of vaccination, and as not vaccinated when less than two weeks had passed after the date of vaccination.
For the analysis of categorical variables we calculated odds ratios (OR) and 95% confidence intervals (CI). We built two models describing the effect of vaccination against pIV and other independent factors on pIV infection, one for children (less than 14 years) and one for “adults” (at least 14 years). We considered as confounders age (as numerical variable), sex, illness week and location of residence, and included in the models those variables that were associated with both pIV infection and vaccination and changed the OR for vaccination by more than 5%. The final model included only the remaining variables as well as illness week. Statistical tests were two-sided and P values of less than 0.05 were considered statistically significant. For calculations we used the software Stata (Stata Corporation, College Station, Texas, USA).
For the case-series method we used all cases of pIV notified through the mandatory notification system where date of disease onset and age was known. Laboratory-confirmed cases of pIV had to be notified by the diagnosing laboratories to the public health system where vaccination status was investigated. Final data were reported via state health departments to the RKI. Hospitalized cases were not excluded, but were rare (less than 2%).
For this method we needed to define a time interval after influenza vaccination when an immune response is beginning to be detectable and when it is fully mounted. According to Brokstad et al.  hemagglutinine antibody titers started to increase after 8–9 days after vaccination. Day 7 would thus be the “last day” in the “unimmune” period and infection on day 7 results in illness on average on day 8 or 9 (adding 1.5–2 days of incubation period). As explained for the test-negative case-control method most vaccinees develop protective antibody titres 2 weeks after vaccination , . We assumed therefore a period of lacking protection after vaccination until day 7 (i.e. day 9 when the day of illness onset is used) and a period of full protection from day 14 after vaccination.
To calculate the VE we assumed that the chance to fall ill and get notified is a proxy for the force of infection that affects all persons. So the cumulative force of infection that a person is exposed to during time t is represented by the number of cases reported during time t. We assume that the chance to be selected for notification is similar in all vaccinated persons during the protected and unprotected phase and we assume that the susceptibility of the people at the time of vaccination is similar to the susceptibility in the population. Susceptibility in the vaccinated group changes in relation to the unvaccinated group from the time of mounted immunity due to induced protection. We assumed further that persons who were immunized were not protected in the immediate time period after vaccination. Based on these assumptions the number of reported cases in a cohort defined by their vaccination date within a given week during any period is a result of 1. the number of individuals exposed, 2. their susceptibility, and 3. the cumulative risk to become ill and be notified during that period.
As the number of individuals in each weekly vaccinated cohort is unknown but unchanged over time, the ratio of (cumulative force of infection during the unprotected phase/number of cases in the weekly vaccinated cohort during this unprotected phase) to the (cumulative force of infection during the protected phase/number of cases from the cohort during the protected phase) indicates a change in susceptibility which is attributed to the effect of the vaccine.
To determine the force of infection during the unprotected period of a cohort vaccinated in a given week we assumed that on average people were vaccinated (and from thereon exposed to infected cases) after Wednesday. While we calculated the exact difference between vaccination date and illness date in days we used weekly data to calculate the force of infection. For an assumed 9 day unprotected period (to the day of symptom onset) the exposure to infection for a vaccine cohort of week x would be the number of all reported cases (vaccinated and unvaccinated) of week x multiplied with 4/7(exposure time in week x), plus the number of all reported cases of week (x+1) multiplied with 5/7 (exposure time in week (x+1)). For the number of cases vaccinated in week x that occurred within the respective unprotected period of 9 days we counted the number of cases that were vaccinated in week x and had a date of illness onset within 9 days after the date of vaccination. Thus, the reference value for a cohort of week x (term 1) was:
(all reported cases of week x *4/7 + all reported cases of the following week (x+1)* 5/7)/(number of cases during the unprotected period (illness onset within 9 days after vaccination) of the cohort vaccinated in week x)
We then performed the same calculation for the assumed protected period which yielded the number of cases necessary to generate a vaccinated case in the hypothetically protected period ending with week 53/2009. The calculation for the protected period beginning 14 days after vaccination for a weekly cohort would be (term 2):
(sum of all reported cases with illness onset between week (x+2) and week 53)/(number of cases during the protected period among those vaccinated in week x with illness onset between week (x+2) and week 53)
The ratio of both terms (term1/term2) gives the relative risk which – under the null hypothesis – is one if the vaccine had no effect.
For the calculation of the overall effect (pooled for all vaccinated weekly cohorts) we assumed that the relation between the force of infection and the generation of cases is stable over time and simply pooled the numerator and denominator data of the respective terms and weeks to calculate an average of the total VE (appendix).
Regarding the final data set used, we focused on the period from week 44 (when vaccination started) to week 53 when the epidemic virus circulation had largely ceased. Weeks where no vaccinated case was reported neither in the unprotected nor in the protected period, were excluded. We conducted the following two sensitivity analyses: (a) for the determination of the force of infection we included only cases with known age and illness onset; however, cases with unknown vaccination status were excluded or included; (b) the unprotected period was varied lasting for 6,7,8,9 or 11 days, respectively (keeping the assumed protected period constant beginning 15 days after vaccination).
The relative risks were calculated for each week of vaccination and for two age groups (less than 14 years, 14 years or above). We report relative risks for weekly cohorts of vaccination as well as an overall estimate for all persons vaccinated.
Laboratory test-negative case-control method
There were 6,195 samples of patients with illness onset between week 44/2009 and 07/2010. Of these, 2,837 (46%) were positive for pIV (Tab. 1). Information on explanatory variables was available in 43% (underlying illness; minimum) up to 99% (age). Median age was 12 years (interquartile range: 6–26 years). Hundred twenty-six patients were reported to be vaccinated against pIV. Of these, information on vaccination date was available for 94 (75%). Among patients with vaccination date data, the proportion of positive samples (positivity rate) dropped with increasing interval between vaccination and disease onset. In 42 patients illness onset was later than 14 days after vaccination with the pandemic vaccine representing 1% of patients with information on vaccine status. Twenty-seven (64%) of the 42 patients were aged younger than 14 years of age and 15 (36%) were 14 years or older. For analysis of the VE, only patients could be included who were known to be unvaccinated or who were vaccinated and where date of vaccination was available. This was the case for 3,836 patients (Fig. 1). ILI cases with information about their vaccination status were more likely to be children compared to ILI cases without information about their vaccination status. Other variables, such as sex, positivity to pIV and chronic underlying disease were not significantly different between the two groups.
Figure 1. Breakdown of population according to vaccination status, test-negative case-control method.doi:10.1371/journal.pone.0019932.g001
Table 1. Basic data used in the test-negative case-control study and the case-series study.doi:10.1371/journal.pone.0019932.t001
Of 1,749 pIV cases six (0.3%) were vaccinated more than 14 days before illness onset, of 2,087 test-negative individuals 36 (1.7%) were vaccinated. The six vaccinated cases were all treated by different physicians. Four (67%) were younger than 14 years (9–13 years), and of these 2 had an underlying chronic condition; two (33%) were at least 14 years old (51 and 64 years), and of these, one had a chronic underlying condition.
In univariate analysis, vaccination against pIV was associated with pIV infection with an OR of 0.17 (95% CI = 0.06–0.40; P<0.001), however, vaccination against seasonal influenza (OR = 0.91; 95% CI = 0.95–1.10; P = 0.34) and underlying disease (OR = 0.84; 95% CI = 0.69–1.04; P value = 0.10) were not. Positivity rate differed by age. It first increased up to 10 years of age and then declined thereafter (Fig. 2). Also male sex (OR = 1.14; 95% CI = 1.03–1.26; P = 0.01) was significantly associated with pIV infection. Positivity rate varied by week of illness onset with a plateau between week 44 up to week 52 and declined thereafter.
Figure 2. Proportion of positive samples (positivity rate) by age.
Points are located at the mean of the ages in the age groups; Germany 2009/2010.doi:10.1371/journal.pone.0019932.g002
After multivariate logistic regression the model for children included the variables vaccination against pIV, age and illness week, and the model for adults contained the variables vaccination against pIV, age, illness week and state of residence (Tab.e 2). In children vaccination against pIV had an OR of 0.21 (Tab. 2) yielding an effectiveness of 79% (95% CI = 35%–93%; P = 0.007). In the age group 14 years and above, vaccination against pIV had an OR of 0.30 for an effectiveness of 70%, but this result was not statistically significant (P = 0.13; Tab. 2).
Table 2. Multivariate logistic regression model, test-negative case-control method.doi:10.1371/journal.pone.0019932.t002
In the period from week 44/2009 to week 53/2009 102,454 cases with a known date of illness onset and age were reported. Of these, vaccination status was known for 73,280 cases (71%). The number of vaccinated cases by interval between vaccination date and illness onset started with a peak on the first day after vaccination and decreased then rapidly to very low numbers by day 10–14 (Fig. 3). The distribution of the number of vaccinated cases by age group was bimodal with one peak at the age group 11–15 years and a second at 46–50 years. Figure 4 shows the total number of cases by week of illness onset as well as the number of vaccinated cases by week of vaccination. The shape of the curve of vaccinated cases by week of vaccination is similar to that of the number of reported cases. The expected number of vaccinated cases during their protected period (assuming that VE is 0%) differs markedly from the curve with the actual number of vaccinated cases during the protected period (Fig. 4).
Figure 3. Vaccinated cases by time between vaccination and Illness.
Frequency of reported and vaccinated laboratory-confirmed cases of pandemic influenza H1N1(2009) by interval between vaccination and illness onset; weeks of illness onset 44–53/2009; Germany.doi:10.1371/journal.pone.0019932.g003
Figure 4. Case-series method.
Frequency of total number of cases with known age and onset of illness (grey, left y-axis), of vaccinated cases by week of vaccination (dashed grey line; right y-axis), vaccinated cases by week of illness onset (unprotected period; dashed-dotted line; right y-axis), vaccinated cases by week of illness onset (protected period; black line; right y-axis) and vaccinated cases by week of illness onset that would be expected if the vaccine had no effect (protected period; dashed black line; right y-axis), Germany; week 44–53, 2009.doi:10.1371/journal.pone.0019932.g004
The VE estimates for the different weekly cohorts is relatively stable within the two age segments despite the low numbers of vaccinated cases (Tab. 3; Fig. 5). In the sensitivity analysis, neither choosing different lengths of the unprotected period (6,7,8,9 and 11 days, respectively) nor the inclusion or exclusion of cases where the exact vaccination status is unknown (for the parameter “total number of reported cases”) has a marked effect on the estimated VE. The confidence intervals of the weekly cohorts overlap. The main influence seems to be age. Overall VE is higher in children compared to adults. The range of the overall point estimates is 86–89% in children and 69–75% in adults, for the weekly cohorts it ranges from 71–90% in children and from 58–85% in adults. All point estimates are statistically significant. Excluding people over the age of 60 from analysis in the case-series method raises the VE estimate by 5% for the age group 14–60 years.
Figure 5. Vaccine effectiveness by weekly cohort.
Vaccine effectiveness of pandemic AS03-adjuvanted vaccine, by weekly vaccinated cohort; case-series method; force of infection is represented by all reported cases with available information on age, illness onset and vaccination status; for methods: see text; up = unprotected period, pp = protected period, pv = post vaccination.doi:10.1371/journal.pone.0019932.g005
Based on data from virologic surveillance as well as from the notifiable disease surveillance system we have found evidence for a good clinical protective effect of the AS03-adjuvanted vaccine that was used in Germany against pIV in autumn of 2009. This finding is corroborated by three results: (1) The positivity rate of vaccinated persons decreased with increasing interval between vaccination date and illness date; (2) the number of vaccinated cases in the database of reported cases decreased to low numbers for those who were vaccinated more than 10–14 days before illness onset (Fig. 2); (3) using two different data sources and two different statistical methods have led to similar point estimates of effectiveness in two age strata.
The dataset used for the test-negative case-control method comprises detailed data from sentinel physicians, but the number of vaccinated cases was small. The dataset from the mandatory notification system - used for the case-series method - comprised in principle data from all physicians and hospitals who diagnose pIV, is many-fold larger but includes fewer patient parameters. Due to these differences, not all stratifications or analyses were similarly possible for both methods. In both datasets persons over 60 years were rare; excluding them in the case-series method would have led to an increase of 5% in the 14–60 year old age group indicating a relatively lower protection in the elderly.
The test-negative case-control method was first described by Skowronski  and Uphoff . It provides a convenient set of controls and can control for a number of covariates if collected. It is based on the assumption that vaccinated patients consult their physician with the same likelihood as non-vaccinated patients when developing ILI and that influenza is detected with the same likelihood if present . To reduce the chance for false negative results we restricted our analysis to test-negative ILI patients whose samples were taken no later than 4 days after disease onset. Because RT-PCR is highly specific (> = 99%), the probability for a false positive sample is very low.
The case-series method is applicable to routinely collected data. Although the unprotected period was short and the number of vaccinees among reported cases low, the method gave reasonable results. Estimates for weekly cohorts do not differ significantly from each other and from the estimate for the total season. Overall, VE estimates of the weekly age group cohorts are all above 50% and it is reassuring that they vary within a rather narrow corridor (Fig. 5). It has to be noted that we have not weighted the estimate of the VE for the total season because the size of the weekly cohorts was unknown (see Fig. S1 and Appendix S1). However, even a weighted estimate should be very similar because the weekly estimates lie within a close range. To further refine the methodology to calculate an overall estimate, approaches such as those used in meta analysis, may be considered .
Both methods were able to take into account that the epidemic wave evolved at the same time with the vaccination campaign. To do this, the test-negative case-control method added illness week into the multivariate model while the case-series method used the number of incident reported cases by week to calculate the proportion of expected vaccinated cases if the vaccine had no effect. A strength of both methods is that selection processes have limited effect because they apply equally to the entire study population.
Vaccination against seasonal influenza was not significantly associated with pIV infection. Several articles have published their analyses regarding the effect of seasonal trivalent influenza on the occurrence of pIV infection, but results were contradictory. A lack of effect , , , a preventive effect ,  and even a “harmful” effect have all been reported . With the power available in our dataset we would have detected even a small effect, for example if the OR for pIV would have been greater than 1.2 or smaller than 0.8.
Because the vaccine used in Germany was a vaccine adjuvanted by the squalen AS03 we cannot make statements about non-adjuvanted vaccines which may have different VE than the one used in Germany. When we attempted to compare our results with studies on the efficacy of squalen-adjuvanted seasonal influenza vaccines, we were unable to identify any in the published literature. However, clinical protection against seasonal influenza provided by inactivated, non-adjuvanted vaccines has been reviewed by Nichol who based her assessment on several published meta-analyses of mostly randomized controlled trials . Depending on the results of different meta-analyses, effectiveness against laboratory-confirmed influenza in children ranged from 54–65% and in younger adults (aged younger than 65 years) from 63–80%. For elderly (aged more than 60 years) the only conducted randomized controlled trial found an efficacy of 58% . With all due caution the effectiveness presented in this paper seems to be better for children and comparable in younger adults.
Our methods have several limitations. The case-series method is prone to influences biasing the case count during the unprotected period versus the protected period. This may be the case if physicians tend to sample vaccinated persons in the two weeks after vaccination more than in the protected period or if vaccinated persons get vaccinated when they become aware of influenza cases in their (private) surrounding, but are less eager to become vaccinated when the epidemic wave has passed and the risk has therefore diminished. Then the decision to become vaccinated and the risk for infection in the unprotected period may reflect to some degree not only the force of infection in the population as a whole but particularly in their immediate environment. However, the distribution of cases after vaccination (Fig. 3) does not suggest that these potential biases are of substantial magnitude.
On a similar note, we have not taken into account the dynamic geographical course of the epidemic which also may have affected vaccination and disease status. Here, two scenarios are possible: (i) individuals have been vaccinated when the epidemic was approaching (staggered vaccination), (ii) individuals have been vaccinated when the vaccine became available (vaccination largely at the same time). Some simple calculations simulating the first scenario showed small deviations of about 5% of the calculated vaccine effectiveness; however, in the scenario where most persons were vaccinated in the first weeks when the vaccine became available, i.e. vaccination was mainly triggered by availability of the vaccine, would not have resulted in a different effectiveness. As it turned out vaccination coverage remained low in Germany as only 8% of the population was vaccinated . In particular, during the start of the campaign it was focused on priority groups, such as health care personnel, first responders, persons with chronic underlying diseases and pregnant women. Scenario two seems therefore more realistic. Another way to analyse this issue would have been to stratify by geographical region which would have necessitated a larger number of vaccinated cases than were available.
In the case series method it was necessary to use cut-off points for the end of the unprotected and the beginning of the protected period after vaccination which could be challenged. The work by Brokstad et al. showed an increase in antibody titers 8–9 days post vaccination . After that an increase roughly following a saturation curve can be expected resulting in protective antibody titres in the majority of vaccinees about two weeks post vaccination . Data from recent studies confirm these findings also for the pandemic vaccine , . To explore the influence of different cut-off points on the VE estimates we had calculated the effect when the unprotected period was assumed to last until day 6,7,8,9 and 11 post vaccination. Lowering the unprotected period from 9 to 6 days increased the VE stepwise to roughly 3% at day 6, and dropped by 2% when the unprotected period was extended to 11 days. We concluded that the choice of the cut-off for the unprotected period is minor and that the results generated by the method are fairly robust. Nevertheless, a degree of imprecision remained because we used weekly values for the force of infection and the assumption that the cohort had been vaccinated by Wednesday.
Compared to our estimates, a recent publication using the screening method found a higher VE than presented here (97% for persons aged 14–59 years, 83% for persons 60 years and older) . In general, the screening method may encounter difficulties when assessing VE during an ongoing vaccination campaign because the dynamic of the epidemic, the change of the proportion vaccinated in the population over time and the time that vaccinations need to take effect need to be considered. In the above mentioned paper, the authors tried to take these issues into account by beginning their study period three weeks after initiation of the vaccination campaign when estimated vaccination coverage in the population was already 4%, and coverage increased only by an additional 3% over the next 3 months . In addition, selection processes like a lower likelihood to swab vaccinated persons or different laboratory sensitivity for different age groups in relation to the proportion vaccinated in these age groups may influence the estimated VE. A case control study from England and a European multicenter case control study showed similar estimates than our study (71%  and 72% (imputation) or 66% respectively). One study found indications for a lower protection in the elderly  and the other study indicated a higher protection in the younger age group , which is in line with the results of our study. Interestingly one study indicated a possible protection in the period 8 to 14 days after vaccination which potentially may challenge the assumption of a negligible protection in the first seven days after vaccination . However the confidence intervals of the estimation are very wide. In our data we observed a very steep drop of cases 7 to 9 days after vaccination (Fig. 3) suggesting that immunity starts to take effect approximately one week after vaccination. A thorough comparison of all methods and findings (including other studies) may give more insight to explain differing results.
In conclusion both methods provided evidence for the good VE of the AS03-adjuvanted vaccine against the pandemic virus A/(H1N1) 2009. Should this virus remain the dominant virus or one of the viruses circulating in the human population, this or a similar vaccine should provide satisfactory protection against disease.
pooling the over all-VE based on the weekly cohorts.
Formula used for pooling the over all-VE based on the weekly cohorts: With: - RR = relative risk - x ranges from 44 (the first week where vaccination started in an organized fashion) to 49 (where vaccination activity and the epidemic declined) - for all weeks to be considered there must be two or more cases in the unprotected and protected period in the cohort vaccinated in week x - y = interval in days chosen from vaccination until illness onset (unprotected period).
We thank the sentinel physicians for sending swabs to the national reference center for influenza, and the state laboratories, particularly Margot Bayer, for managing a large number of samples from Bavaria; the local health departments for their efforts to investigate the details of many pIV cases regarding their vaccination status; Niko Stilianakis for critical reading of the manuscript; and Marcel Feig for data support.
Conceived and designed the experiments: HU UB BS WH SB TE DF HC DB CH ML. Performed the experiments: HU UB BS WH SB TE DF HC DB CH ML. Analyzed the data: UB HU MH DA SB DF. Contributed reagents/materials/analysis tools: UB HU MH BS SB WH DF DA OW TE HC DB CH MLMF. Wrote the paper: UB HU MH TE WH SB. Contributed revised data: DA TE OW DF MF. Contributed comments: SB WH OW TE MH.
- 1. Anonymous (2007) National pandemic plan [Nationaler Pandemieplan]. www.rki.de/cln_169/nn_1731376/DE/Content/InfAZ/I/Influenza/influenzapandemieplan__III,templateId=raw,property=publicationFile.pdf/influenzapandemieplan_III. Chapter 6.2.1.
- 2. Zhu FC, Wang H, Fang HH, Yang JG, Lin XJ, et al. (2009) A novel influenza A (H1N1) vaccine in various age groups. N Engl J Med 361: 2414–2423.
- 3. Clark TW, Pareek M, Hoschler K, Dillon H, Nicholson KG, et al. (2009) Trial of 2009 influenza A (H1N1) monovalent MF59-adjuvanted vaccine. N Engl J Med 361: 2424–2435.
- 4. Glaxo , Smith , Kline (October 23, 2009) Pandemic (H1N1) 2009 Influenza Update: Experience of GSK's H1N1 adjuvanted vaccine, Pandemrix™, and preliminary paediatric results. Press release.
- 5. Anonymous (2009) Empfehlungen der Ständigen Impfkommission (STIKO) am Robert Koch Institut, 12.Oktober 2009. [Recommendations of the Standing Committee for Vaccination at the Robert Koch-Institute]. Epidemiologisches Bulletin 403–425.
- 6. Anonymous (2009) Mitteilung der Ständigen Impfkommission (STIKO) am Robert Koch-Institut zur Impfung gegen die Neue Influenza A (H1N1): Erneute Bewertung der Daten am 24.11.2009 [Statement of the Standing Committee for Vaccine Recommendations at the Robert Koch-Institute on the vaccination against Novel Influenza A(H1N1): updated assessment of data on Nov 24, 2009]. Epidemiologisches Bulletin 514–520.
- 7. Orenstein EW, De Serres G, Haber MJ, Shay DK, Bridges CB, et al. (2007) Methodologic issues regarding the use of three observational study designs to assess influenza vaccine effectiveness. Int J Epidemiol 36: 623–631.
- 8. Whitaker HJ, Farrington CP, Spiessens B, Musonda P (2006) Tutorial in biostatistics: the self-controlled case series method. Stat Med 25: 1768–1797.
- 9. ECDC (Stockholm, Sweden. November 2009) Protocol for case-control studies to measure influenza vaccine effectiveness in the European Union and European Economic Area Member States. http://www.ecdc.europa.eu/en/publications/Publications/0907_TED_Influenza_AH1N1_Measuring_Influenza_Vaccine_Effectiveness_Protocol_Case_Control_Studies.pdf.
- 10. Cox RJ, Haaheim LR, Ericsson JC, Madhun AS, Brokstad KA (2006) The humoral and cellular responses induced locally and systemically after parenteral influenza vaccination in man. Vaccine 24: 6577–6580.
- 11. Clark TW, Pareek M, Hoschler K, Dillon H, Nicholson KG, et al. (2009) Trial of 2009 Influenza A(H1N1) monovalent MF59-adjuvated vaccine. N Engl J Med 361: 2424–2435.
- 12. Brokstad KA, Cox RJ, Major D, Wood JM, Haaheim LR (1995) Cross-reaction but no avidity change of the serum antibody response after influenza vaccination. Vaccine 13: 1522–1528.
- 13. Skowronski DM, Gilbert M, Tweed SA, Petric M, Li Y, et al. (2005) Effectiveness of vaccine against medical consultation due to laboratory-confirmed influenza: results from a sentinel physician pilot project in British Columbia, 2004–2005. Can Commun Dis Rep 31: 181–191.
- 14. Uphoff H, Hauri AM, Schweiger B, Heckler R, Haas W, et al. (2006) Zur Schätzung der Schutzwirkung der Influenzaimipfung aus Surveillancedaten [Estimation of influenza vaccine effectiveness using routine surveillance data]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz 49: 287–295.
- 15. Blettner M, Sauerbrei W, Schlehofer B, Scheuchenpflug T, Friedenreich C (1999) Traditional reviews, meta-analyses and pooled analyses in epidemiology. Int J Epidemiol 28: 1–9.
- 16. France AM, Jackson M, Schrag S, Lynch M, Zimmerman C, et al. (2010) Household transmission of 2009 influenza A (H1N1) virus after a school-based outbreak in New York City, April–May 2009. J Infect Dis 201: 984–992.
- 17. (2009) Effectiveness of 2008–09 trivalent influenza vaccine against 2009 pandemic influenza A (H1N1) - United States, May–June 2009. MMWR Morb Mortal Wkly Rep 58: 1241–1245.
- 18. Kelly H, Grant K (2009) Interim analysis of pandemic influenza (H1N1) 2009 in Australia: surveillance trends, age of infection and effectiveness of seasonal vaccination. Euro Surveill 14:
- 19. Echevarria-Zuno S, Mejia-Arangure JM, Mar-Obeso AJ, Grajales-Muniz C, Robles-Perez E, et al. (2009) Infection and death from influenza A H1N1 virus in Mexico: a retrospective analysis. Lancet 374: 2072–2079.
- 20. Garcia-Garcia L, Valdespino-Gomez JL, Lazcano-Ponce E, Jimenez-Corona A, Higuera-Iglesias A, et al. (2009) Partial protection of seasonal trivalent inactivated vaccine against novel pandemic influenza A/H1N1 2009: case-control study in Mexico City. Bmj 339: b3928.
- 21. Skowronski DM, De Serres G, Crowcroft NS, Janjua NZ, Boulianne N, et al. (2010) Association between the 2008–09 seasonal influenza vaccine and pandemic H1N1 illness during Spring–Summer 2009: four observational studies from Canada. PLoS Med 7: e1000258.
- 22. Nichol KL (2008) Efficacy and effectiveness of influenza vaccination. Vaccine 26: Suppl 4D17–22.
- 23. Govaert TM, Thijs CT, Masurel N, Sprenger MJ, Dinant GJ, et al. (1994) The efficacy of influenza vaccination in elderly individuals. A randomized double-blind placebo-controlled trial. Jama 272: 1661–1665.
- 24. RKI (2010) Pandemische Influenza (H1N1) 2009 – Ergebnisse zweier Befragungen. Epidemiologisches Bulletin 13: 112–115.
- 25. Valenciano M, Kissling E, Cohen J-M, Oroszi B, Barret A-S, Rizzo C, Nunes B, et al. (2011) Estimates of pandemic Influenza vaccine effectiveness in Europe, 2009–2010: Results of Influenza monitoring vaccine effectiveness in Europe (I-Move) multicentre case-control study. PLoS Med 7: e1000388.
- 26. Wichmann O (2010) Pandemic influenza A(H1N1) 2009 breakthrough infections and estimates of vaccine effectiveness in Germany 2009–2010. Eurosurveillance weekly 15(8): 2492.
- 27. Hardelid P, Fleming DM, McMenamin J, Andrews A, Robertson C, SebastianPillai P, Ellis J, et al. (2011) Effectiveness of pandemic and seasonal Influenza vaccine in preventing pandemic Influenza A(H1N1) 2009 infection in England and Scotland 2009–2010. Eurosurveillance 16(2): 19763.