- Research article
- Open Access
Comparing influenza vaccine efficacy against mismatched and matched strains: a systematic review and meta-analysis
BMC Medicine volume 11, Article number: 153 (2013)
Influenza vaccines are most effective when the antigens in the vaccine match those of circulating strains. However, antigens contained in the vaccines do not always match circulating strains. In the present work we aimed to examine the vaccine efficacy (VE) afforded by influenza vaccines when they are not well matched to circulating strains.
We identified randomized clinical trials (RCTs) through MEDLINE, EMBASE, the Cochrane Library, and references of included RCTs. RCTs reporting laboratory-confirmed influenza among healthy participants vaccinated with antigens of matching and non-matching influenza strains were included. Two independent reviewers screened citations/full-text articles, abstracted data, and appraised risk of bias. Conflicts were resolved by discussion. A random effects meta-analysis was conducted. VE was calculated using the following formula: (1 - relative risk × 100%).
We included 34 RCTs, providing data on 47 influenza seasons and 94,821 participants. The live-attenuated influenza vaccine (LAIV) showed significant protection against mismatched (six RCTs, VE 54%, 95% confidence interval (CI) 28% to 71%) and matched (seven RCTs, VE 83%, 95% CI 75% to 88%) influenza strains among children aged 6 to 36 months. Differences were observed between the point estimates for mismatched influenza A (five RCTs, VE 75%, 95% CI 41% to 90%) and mismatched influenza B (five RCTs, VE 42%, 95% CI 22% to 56%) estimates among children aged 6 to 36 months. The trivalent inactivated vaccine (TIV) also afforded significant protection against mismatched (nine RCTs, VE 52%, 95% CI 37% to 63%) and matched (eight RCTs, VE 65%, 95% CI 54% to 73%) influenza strains among adults. Numerical differences were observed between the point estimates for mismatched influenza A (five RCTs, VE 64%, 95% CI 23% to 82%) and mismatched influenza B (eight RCTs, VE 52%, 95% CI 19% to 72%) estimates among adults. Statistical heterogeneity was low (I2 <50%) across all meta-analyses, except for the LAIV meta-analyses among children (I2 = 79%).
The TIV and LAIV vaccines can provide cross protection against non-matching circulating strains. The point estimates for VE were different for matching versus non-matching strains, with overlapping CIs.
Influenza is a major public health threat. It is widely accepted that an annual influenza vaccination is the most effective way to prevent influenza . Among adults, for example, the inactivated influenza vaccine was reported to have a vaccine efficacy (VE) of 59% (95% confidence interval (CI) 51 to 67) .
Recommendations for influenza vaccine composition currently include two type A influenza strains (A-H3N2 and A-H1N1) and one type B influenza strain, which are updated annually. Strains are selected by scientists convened by the World Health Organization (WHO)  in the months before the next epidemic season is expected. This procedure includes consideration of antigenic mismatch between vaccine strains and actual epidemic strains.
Although it is accepted that matched strains provide the best protection, data on the protective efficacy of unmatched strains, or cross protection, are sparse. These data are of particular importance, given that influenza B vaccine strains did not match circulating strains in six influenza seasons between 2000 and 2011 in the USA . Mismatched seasons may lead to reduced uptake of influenza vaccination, reduced VE, and more severe influenza epidemics. Therefore, estimating prevention that can be achieved during mismatched influenza seasons is of prime public health importance. This information cannot be gleaned from previous reviews on the efficacy of the influenza vaccines because they did not specifically examine vaccine efficacy for mismatched seasons [5–7]. As such, in the present work we aimed to determine the cross protection against laboratory-confirmed influenza through vaccination.
The Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement was used to guide the reporting and conduct of this review . A systematic review protocol was compiled and circulated to experts in influenza, systematic reviews, and statistics. The protocol was registered with PROSPERO, an international registry for systematic reviews (CRD42012001926) and published in an open-access journal .
Studies reporting the incidence of influenza infection after vaccination among healthy individuals were included. The primary outcome was the incidence of laboratory-confirmed influenza verified by polymerase chain reaction (PCR) or viral culture. The secondary outcome was the incidence of laboratory-confirmed influenza verified by at least a fourfold rise in hemagglutinin inhibition (HI) antibody titers at the end of the influenza season versus baseline (serologic assay) or serologic assay in combination with another detection method (for example, viral culture or PCR). Randomized clinical trials (RCTs) and quasi-RCTs (that is, use of non-random methods to allocate patients to the treatment and control groups, such as consecutive enrolment or the last digit of a health card number) comparing any influenza vaccine versus placebo and disseminated in the English language were included.
Study selection process
The eligibility criteria were pilot tested on a random sample of 50 citations and clarified, as needed. Two reviewers subsequently screened titles and abstracts (citations) from the literature search in duplicate. Conflicts were resolved through team discussion. A similar process was followed for screening potentially relevant full-text articles identified through citation screening.
Information sources and search
The full search strategy is reported elsewhere . Briefly, RCTs were identified by searching three Cochrane reviews on influenza vaccines [5–7], MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, meta-Register (a clinical trials registry), and the references of included trials. The literature searches were conducted by an experienced librarian on 31 January 2012.
Data items and collection process
The data abstracted included study characteristics, participant characteristics, and number of influenza cases per treatment group, confirmed by viral culture, PCR or serologic assay. A data abstraction form was developed and pilot tested. Two reviewers subsequently abstracted all of the data in duplicate. Discrepancies were resolved by discussion. Trial authors were contacted for data clarifications and additional unpublished data was received from six included published RCTs [10–15].
Risk of bias appraisal
The Cochrane Risk of Bias seven-item tool was used to appraise the likelihood that the RCT results were affected by bias . For the selective outcome reporting criterion, trial protocols were obtained and the outcomes reported in the protocol were compared to those reported in the final trial publication. For the other sources of bias criterion, industry-funded RCTs were scored as ‘unclear’, due to the potential for funding bias .
We also assessed other methodological issues identified a priori that are related to influenza and may have influenced the RCT results. These included case definitions used by health care workers to identify influenza-like illness (ILI), use of a surveillance system to monitor influenza cases, and randomization scheme across multisite trials. Case definition of influenza-like illness was defined according to the Centers for Disease Control and Prevention (CDC) as fever >37.8°C (100°F) with cough and/or sore throat . Surveillance system was defined as a system to track ILI in the population and consisted of health care workers contacting participants to monitor ILI symptoms. Randomization scheme referred to the consistent use of an allocation schedule across trial study sites for multisite trials.
Characterization of matched or mismatched vaccine strains
The process of characterizing matched versus mismatched strains was determined a priori and involved the two steps outlined below.
Viral strains from influenza cases in the included RCTs were characterized through HI assays using vaccine strains as the reference. Influenza A strains from infected trial participants were matched with the strain in the vaccine if they belonged to the same A subtype (that is, H1N1 or H3N2) and were antigenically similar in the HI assay (that is, if they showed sufficient crossreaction in a HI chessboard table using ferret antisera; for example, with a HI typing quotient <fourfold titer). Influenza A viral strains were considered mismatched by antigenic drift if they were antigenically distinct from influenza A strains contained in the vaccine as per HI typing (for example, HI titer quotient ≥fourfold) or the characterization did not belong to a similar influenza A subtype contained in the vaccine (for example, H1N1 strains circulating but only H3N2 strains contained in the vaccine for bivalent vaccines with one H subtype).
For influenza B, the epidemiological situation is more complex. In recent years, there have been two coexisting phylogenetic influenza B lineages: B/Victoria and B/Yamagata [19, 20]. Influenza B strains from infected trial participants were considered matched if the strain belonged to the same lineage and were antigenically similar to the vaccine strain as per HI typing (for example, HI typing quotient <fourfold titer). For influenza B mismatches, two different forms were considered. Mismatch by antigenic drift refers to strains of the same lineage that were antigenically distinct from influenza B strains contained in the vaccine as per HI typing (for example, HI quotient ≥fourfold titer), whereas mismatch by lineage refers to influenza B strains of different lineages. Whenever the influenza B lineage was not presented in the trial report, categorization was based on the influenza phylogenetic tree and verified by influenza experts on the team.
When antigenic characterization of viral strains of infected participants was not reported, data from surveillance systems were used to determine circulating strains that occurred during the time and location of the trial conduct. These included WHO weekly epidemiological records, Mortality and Morbidity Reports Weekly (MMRW), Chinese National Influenza Center, and CDC influenza summary reports. These data were sometimes captured through correspondence with trial authors.
Synthesis of included studies
The relative risk (RR) was calculated for the number of influenza cases per treatment group for included RCTs and 95% confidence intervals (CIs) were derived based on a normal approximation. Meta-analysis was conducted using a random effects model  for the live attenuated influenza vaccines (LAIV), trivalent inactivated vaccines (TIV), and other vaccines, separately. A post hoc sensitivity analysis was also conducted to examine the influence of categorizing the vaccines as being either an inactivated influenza vaccine or a live influenza vaccine. VE was derived based on pooled RRs using the following formula: (1 - RR) × 100%. Only influenza infections due to mismatched strains were included in the mismatched analysis, while only influenza infections due to matched strains were included in the matched analysis.
To assess for clinical and methodological heterogeneity, we examined the forest plots from the meta-analysis. The similarity between studies regarding participant and study characteristics was considered and subgroup analysis was conducted. Subgroup analyses determined a priori included age group (children <18 years of age, adults ≥18 years of age, older patients ≥65 years of age) and type of influenza (A versus B). Statistical heterogeneity was examined using the I2 statistic . Funnel plots were performed to identify potential publication bias . All analyses were conducted in SAS version 9.1 (SAS Inc., Cary, NC, USA).
The literature search resulted in a total of 1,356 citations, of which 308 were deemed potentially relevant (Figure 1). Reasons for exclusion at the full-text level of screening included not laboratory-confirmed influenza (108/273), no comparison to placebo (82/273), not a RCT (68/273), not a healthy population (11/273), not vaccinated against influenza A or B (3/273), and not disseminated in English (1/273). A total of 34 trials fulfilled the inclusion criteria [10–15, 24–51] plus 1 companion report , which was used for supplementary data only (hence a total of 35 RCTs). In all, 32 RCTs [10–15, 25–27, 29–51] and 2 quasi-RCTs [24, 28] provided data on 47 influenza seasons including 94,821 healthy participants.
The trials were conducted between 1970 and 2009 (Table 1) in North America (22/34), Europe (3/34), Australia (1/34), Asia (3/34), and a mixture of multisite trials in North America, Europe, South America, Asia, and South Africa (4/34; Additional file 1). A total of 11 trials examined the TIV versus placebo [15, 28, 30, 34, 38, 39, 44–46, 49],, 7 examined the LAIV versus placebo [10, 35, 37, 40–43] and 6 examined both TIV and LAIV vaccines versus placebo [11, 13, 14, 31, 36, 47]. Other vaccine types were examined in several RCTs, such as monovalent inactivated [24, 25, 51], bivalent attenuated [26, 27], whole-virus vaccine , baculovirus-expressed HI influenza vaccine (rHAO) , and a trivalent recombinant HI protein vaccine . One RCT examined both a TIV and bivalent vaccine compared to placebo .
In all, 22 RCTs (including information on 34 influenza seasons) provided data on matched influenza strains [10, 11, 13–15, 24, 29, 31, 35, 37],[39–43, 45–51], while 20 RCTs (including data from 33 influenza seasons) provided data on mismatched influenza strains [10–15, 26, 29, 31, 37, 40–47, 49, 50] (Table 1). Influenza infection was confirmed by culture in 20 RCTs [10–12, 15, 24, 26, 29, 31, 35, 37],[39–48], PCR in 3 RCTs [14, 50, 51], and culture or PCR in 2 RCTs [13, 49]. Nine RCTs included serologic assays to determine influenza infection; these were included in the secondary analysis only [25, 27, 28, 30, 32–34, 36, 38].
The RCTs included data on a total of 94,821 participants (Table 2). A total of 13 of the RCTs were conducted among children [10, 25, 30, 32, 35, 37, 39–43, 49],, and 2 were conducted among seniors [33, 36]. One RCT included children (15%) and adults (85%) , and another included adults and seniors ; the remaining RCTs were conducted among adults only. The percentage of female participants ranged from 22%  to 100% .
Risk of bias
Of the included trials, only 26% adequately reported sequence generation and 29% adequately reported allocation concealment (Figure 2). The majority of the RCTs blinded participants and physicians (65%) and addressed incomplete data (62%). Only half of the RCTs were deemed to be free from other sources of bias (44%; 56% scored unclear because they were industry funded) and 23% were free from selective outcome reporting (Table 3).
The trials were conducted over 40 years and the risk of bias for older studies was compared to newer studies, using 1991 as the midpoint. No trends were observed for sequence generation or allocation sequence and differences between groups were minimal. Blinding of outcome assessors and the reporting of incomplete data improved in recent studies by 17%. Furthermore, selective outcome reporting in recent studies showed an improvement of 42% in the risk of bias. There was also an increase in the proportion of RCTs scoring ‘unclear’ on other risk of bias criterion, as more trials were funded by private industry in recent years.
Only 15% of trials were free of other methodological issues, which included adequate information on case definition of ILI and surveillance of influenza, as well as details regarding randomization across multiple sites [12, 38, 44, 48, 50] (Additional file 2). Almost half of trials (16 of 34) did not adequately report a case definition of ILI and the remaining studies were unclear in at least 1 of the domains for other methodological concerns.
LAIV versus placebo
The results from all LAIV versus placebo meta-analyses are presented in Additional file 3. For simplicity, we have focused on the results specific to children aged <18 years for the primary outcome.
The LAIV was protective against mismatched strains overall (11 RCTs, VE 60%, 95% CI 44% to 71%; Figure 3; Additional file 3) [10, 11, 13, 14, 31, 37, 40–43, 47], as well as among children aged 6 to 36 months (6 RCTs, VE 54%, 95% CI 28% to 71%) [10, 37, 40–43] when strains were mismatched. Similarly, the LAIV was effective in protecting against infection when circulating strains were well matched overall (12 RCTs, VE 77%, 95% CI 67% to 86%, Figure 4) [10, 11, 13, 14, 31, 35, 37, 40–43],. LAIV provided significant protection among children when circulating strains matched vaccine composition (seven RCTs, VE 83%, 95% CI 75% to 88%) [10, 35, 37, 40–43].
When influenza A strains did not match LAIV composition, protection against infection was statistically significant among children (five RCTs, VE 75%, 95% CI 41% to 90%) [10, 37, 40, 41, 43]. LAIV was also effective in protecting against influenza A when strains were well matched in children (six RCTs, VE 84%, 95% CI 76% to 90%) [10, 35, 40–43].
When influenza B strains were mismatched, LAIV was effective among children (five RCTs, VE 42%, 95% CI 22% to 56%) [10, 40–43]. Furthermore, LAIV was more protective against drifted B strains (two RCTs, VE 62%, 95% CI 21% to 81%) [40, 41] than lineage mismatch for influenza B (five RCTs, VE 34%, 95% CI 4−% to 59%) [10, 40–43] in children. Similarly, LAIV was effective against influenza B when circulating strains matched vaccine strains in children (four RCTs, VE 79%, 95% CI 58% to 90%) [10, 35, 41, 43].
TIV versus placebo
The results from all TIV versus placebo meta-analyses are presented in Additional file 3. For simplicity in the text, we have focused on the results specific to adults aged ≥18 years.
The TIV showed protection against mismatched strains overall (11 RCTs, VE 56%, 95% CI 43% to 66%, Figure 5) [11, 13–15, 31, 44–47, 49, 50] and among adults (9 RCTs, VE 52%, 95% CI 37% to 63%) [11, 13–15, 44–47, 49]. Similarly, TIV vaccines showed protection against matched strains overall (11 RCTs, VE 65%, 95% CI 58% to 72%, Figure 6) [11, 13–15, 31, 39, 45–47, 49, 50] and among adults (8 RCTs, VE 65%, 95% CI 54% to 73%) [11, 13–15, 45–47, 49].
In adults, TIV provided significant protection against mismatched influenza A strains (six RCTs, VE 64%, 95% CI 23% to 82%) [11, 14, 15, 45, 47, 49], and matched influenza A strains (seven RCTs, VE 61%, 95% CI 46% to 73%) [13–15, 45–47, 49]. The TIV also afforded protection against mismatched influenza B strains (eight RCTs, VE 52%, 95% CI 19% to 72%) [11, 13–15, 45–47, 49], as well as matched influenza B strains (four RCTs, VE 77%, 95% CI 18% to 94%) [11, 15, 47, 49] among adults.
Other vaccines compared to placebo
In all, 3 RCTs including 5 influenza seasons and 1,578 participants provided efficacy estimates against mismatched strains for other vaccines [12, 26, 29, 31]. Protection against mismatched strains was statistically significant (three RCTs, VE 56%, 95% CI 23% to 75%) [12, 26, 29].
Other vaccines contributed data on 5 influenza seasons from 4 RCTs including 15,592 participants for matched strains. Other vaccines provided a VE of 54% (four RCTs, 95% CI 5% to 78%) [24, 29, 48, 51].
Post hoc subgroup analysis
Our results did not change after a post hoc sensitivity analysis was conducted to examine the influence of categorizing the vaccines as being either an inactivated influenza vaccine or a live influenza vaccine versus categorizing the vaccines as LAIV, TIV, and other.
In the present work, we conducted a systematic review to estimate the protection afforded by mismatched influenza vaccines. Our results show that mismatched vaccines can reduce the risk of PCR or culture-confirmed influenza by 60% for LAIV (95% CI 44% to 71%) and by 56% for TIV (95% CI 43% to 66%). These results suggest a benefit of vaccines in preventing laboratory-confirmed influenza even when there is a mismatch between vaccine composition and circulating strains. For matched influenza, point estimates for VE were slightly higher for both the LAIV (77%, 95% CI 67% to 86%) and the TIV (65%, 95% CI 57% to 72%), versus mismatched point estimates. However, there was substantial overlap in the CIs for matched and mismatched estimates in some instances; the impact of this overlap could not be formally tested via meta-analyses techniques.
A previous systematic review on a similar topic did not report the results separately for matched or mismatched strains . A Cochrane review among healthy adults found a VE for TIV non-WHO matching strains (including when the specific strains are unknown) of 44% (95% CI 23% to 59%) . This result was based on six influenza seasons from four RCTs. A VE of 68% (95% CI 44% to 81%) was observed for LAIV non-WHO matching strains (including when the specific strains are unknown), based on four point estimates from three RCTs . Our review is based on an additional 13 RCTs and we have included more than double the data for both LAIV and TIV compared to the Cochrane review. Furthermore, here we have followed a rigorous process of identifying matched and mismatched data, which has not been attempted in previous reviews. Our results are consistent with those found in a pooled observational study including 5 years of data .
We found that the LAIV was more efficacious among children versus adults, which is likely a reflection of the difference in previously acquired influenza infections between age groups and the consequently larger amount of pre-vaccination antibody, which affects the live vaccine. However, we found higher point estimates for adults versus children for mismatched LAIV estimates. This finding might suggest that there might be a possible discrepancy in the degree of matching, which may have impacted our results. Specifically, trials conducted among children may have had a greater degree of mismatch than those conducted among adults. Unfortunately, the current analysis does not allow the degree of mismatch to be examined. For the purposes of our analysis, we dichotomized cross protection but in reality, the degree of mismatch is a continuum. The cross protection inferred by mismatch strains should be analyzed as a continuum in the future.
The results from our secondary outcome analysis were often inconsistent with our primary outcome results. This inconsistency is likely due to differences in sensitivity and specificity of different laboratory tests over time. Indeed, the most reliable diagnostic test for clinical practice is PCR so the results from our primary outcome should be considered the most valid [54, 55].
Our results are generalizable to seasonal influenza, as most of the included studies reported on this type of influenza. Only one of the included RCTs occurred during the influenza pandemic . When this study was removed via sensitivity analysis, we did not observe any differences on our meta-analysis results.
We identified three RCTs reporting data among seniors [33, 36, 51], yet none reported our primary outcome of interest or provided data on mismatched influenza. This finding is consistent with previous influenza reviews, for which few RCTs were identified among this age group [2, 5]. Future RCTs are needed in this area to provide patients, healthcare providers, and health policymakers with guidance related to vaccination among seniors during seasons when the vaccine composition does not match circulating strains .
There are a few limitations in the evidence base summarized for this review. Many of the trials had an unclear risk of bias because of poor reporting. However, we did note improvements in risk of bias over time that may be because of uptake of the Consolidated Standards of Reporting Trials (CONSORT Statement), providing guidance on what should be reported in RCTs . Enhanced reporting of outcome definitions might be due to clinical trial registry requirements for trials. We also noted that more trials in this area were funded by industry over time.
Another potential limitation is that although unpublished data was only obtained from six RCTs (Additional file 4), no data were obtained from unpublished RCTs. This finding suggests that we might be missing data from unpublished trials. However, we contacted many trial authors for unpublished data and searched trial registries (for example, meta-Register) to identify potentially relevant unpublished RCTs. Furthermore, our funnel plots did not suggest that publication bias influenced our results .
A critical limitation, which may have influenced our results, is the determination of mismatch between circulating strains and those found in the vaccine. Characterizing strains as antigenically similar or distinct using HI assay or ferret antisera might be insensitive, leading to misclassification of strains . Residual misclassification of matching due to the limited discriminatory ability of H1 assays may have also explained some of our findings, and is a limitation of the inferences that can be made. Furthermore, the cut-off values recommended by the CDC to distinguish between match and mismatch strains using the HI assay changed during the study period across the included RCTs, although most of the studies included here used a fourfold quotient HI cut-off (Table 1). As such, some of the data from trials labeled as matched might actually have been mismatched , and vice versa.
By summarizing the point estimates and confidence intervals for cross protection, these data can help public health officials anticipate the possible infection and complications during mismatched years. Estimates of protection for mismatched influenza seasons can be used by patients who are contemplating immunization, since the LAIV and TIV have been shown to offer benefit during matched seasons, as well as mismatched seasons.
Fiore AE, Uyeki TM, Broder K, Finelli L, Euler GL, Singleton JA, Iskander JK, Wortley PM, Shay DK, Bresee JS, Cox NJ: Prevention and control of influenza with vaccines: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2010. MMWR Recomm Rep. 2010, 59: 1-62.
Osterholm MT, Kelley NS, Sommer A, Belongia EA: Efficacy and effectiveness of influenza vaccines: a systematic review and meta-analysis. Lancet Infect Dis. 2012, 12: 36-44. 10.1016/S1473-3099(11)70295-X.
Ampofo WK, Baylor N, Cobey S, Cox NJ, Daves S, Edwards S, Ferguson N, Grohmann G, Hay A, Katz J, Kullabutr K, Lambert L, Levandowski R, Mishra AC, Monto A, Siqueira M, Tashiro M, Waddell AL, Wairagkar N, Wood J, Zambon M, Zhang W, WHO Writing Group: Improving influenza vaccine virus selection: report of a WHO informal consultation held at WHO headquarters, Geneva, Switzerland, 14–16 June 2010. Influenza Other Respi Viruses. 2012, 6: 142-152. e141-145
Centers for Disease Control and Prevention: Book Seasonal Influenza (Flu)- Past Weekly Surveillance Reports. Seasonal Influenza (Flu)- Past Weekly Surveillance Reports. 2012, Atlanta, GA: Centers for Disease Control and Prevention
Jefferson T, Di Pietrantonj C, Al-Ansary LA, Ferroni E, Thorning S, Thomas RE: Vaccines for preventing influenza in the elderly. Cochrane Database Syst Rev. 2010, 2: CD004876
Jefferson T, Di Pietrantonj C, Rivetti A, Bawazeer GA, Al-Ansary LA, Ferroni E: Vaccines for preventing influenza in healthy adults. Cochrane Database Syst Rev. 2010, 7: CD001269
Jefferson T, Rivetti A, Di Pietrantonj C, Demicheli V, Ferroni E: Vaccines for preventing influenza in healthy children. Cochrane Database Syst Rev. 2012, 8: CD004879
Moher D, Liberati A, Tetzlaff J, Altman DG: Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. BMJ. 2009, 339: b2535-10.1136/bmj.b2535.
Tricco AC, Chit A, Hallett D, Soobiah C, Meier G, Chen M, Tashkandi M, Bauch C, Loeb M: Effect of influenza vaccines against mismatched strains: a systematic review protocol. Syst Rev. 2012, 1: 35-10.1186/2046-4053-1-35.
Bracco Neto H, Farhat CK, Tregnaghi MW, Madhi SA, Razmpour A, Palladino G, Small MG, Gruber WC, Forrest BD: Efficacy and safety of 1 and 2 doses of live attenuated influenza vaccine in vaccine-naive children. Pediatr Infect Dis J. 2009, 28: 365-371. 10.1097/INF.0b013e31819219b8.
Ohmit SE, Victor JC, Rotthoff JR, Teich ER, Truscon RK, Baum LL, Rangarajan B, Newton DW, Boulton ML, Monto AS: Prevention of antigenically drifted influenza by inactivated and live attenuated vaccines. N Engl J Med. 2006, 355: 2513-2522. 10.1056/NEJMoa061850.
Treanor JJ, Schiff GM, Hayden FG, Brady RC, Hay CM, Meyer AL, Holden-Wiltse J, Liang H, Gilbert A, Cox M: Safety and immunogenicity of a baculovirus-expressed hemagglutinin influenza vaccine: a randomized controlled trial. JAMA. 2007, 297: 1577-1582. 10.1001/jama.297.14.1577.
Ohmit SE, Victor JC, Teich ER, Truscon RK, Rotthoff JR, Newton DW, Campbell SA, Boulton ML, Monto AS: Prevention of symptomatic seasonal influenza in 2005-2006 by inactivated and live attenuated vaccines. J Infect Dis. 2008, 198: 312-317. 10.1086/589885.
Monto AS, Ohmit SE, Petrie JG, Johnson E, Truscon R, Teich E, Rotthoff J, Boulton M, Victor JC: Comparative efficacy of inactivated and live attenuated influenza vaccines. N Engl J Med. 2009, 361: 1260-1267. 10.1056/NEJMoa0808652.
Jackson LA, Gaglani MJ, Keyserling HL, Balser J, Bouveret N, Fries L, Treanor JJ: Safety, efficacy, and immunogenicity of an inactivated influenza vaccine in healthy adults: a randomized, placebo-controlled trial over two influenza seasons. BMC Infect Dis. 2010, 10: 71-10.1186/1471-2334-10-71.
Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, Savovic J, Schulz KF, Weeks L, Sterne JA: The Cochrane Collaboration’s tool for assessing risk of bias in randomised trials. BMJ. 2011, 343: d5928-10.1136/bmj.d5928.
Lexchin J, Bero LA, Djulbegovic B, Clark O: Pharmaceutical industry sponsorship and research outcome and quality: systematic review. BMJ. 2003, 326: 1167-1170. 10.1136/bmj.326.7400.1167.
American College Health Association: Influenza-like illness case definition. http://www.acha.org/ILI_Project/ILI_case_definition_CDC.pdf.
Shaw MW, Xu X, Li Y, Normand S, Ueki RT, Kunimoto GY, Hall H, Klimov A, Cox NJ, Subbarao K: Reappearance and global spread of variants of influenza B/Victoria/2/87 lineage viruses in the 2000–2001 and 2001–2002 seasons. Virology. 2002, 303: 1-8. 10.1006/viro.2002.1719.
Rota PA, Wallis TR, Harmon MW, Rota JS, Kendal AP, Nerome K: Cocirculation of two distinct evolutionary lineages of influenza type B virus since 1983. Virology. 1990, 175: 59-68. 10.1016/0042-6822(90)90186-U.
DerSimonian R, Laird N: Meta-analysis in clinical trials. Controlled Clin Trials. 1986, 7: 177-188. 10.1016/0197-2456(86)90046-2.
Higgins JP, Thompson SG: Quantifying heterogeneity in a meta-analysis. Stat Med. 2002, 21: 1539-1558. 10.1002/sim.1186.
Egger M, Davey Smith G, Schneider M, Minder C: Bias in meta-analysis detected by a simple, graphical test. BMJ. 1997, 315: 629-634. 10.1136/bmj.315.7109.629.
Leibovitz A, Coultrip RL, Kilbourne ED, Legters LJ, Smith CD, Chin J, Schulman JL: Correlated studies of a recombinant influenza-virus vaccine. IV. Protection against naturally occurring influenza in military trainees. J Infect Dis. 1971, 124: 481-487. 10.1093/infdis/124.5.481.
Beutner KR, Chow T, Rubi E, Strussenberg J, Clement J, Ogra PL: Evaluation of a neuraminidase-specific influenza A virus vaccine in children: antibody responses and effects on two successive outbreaks of natural infection. J Infect Dis. 1979, 140: 844-850. 10.1093/infdis/140.6.844.
Rytel MW, Jackson LJ, Niebojewski RA, Haagensen JL, Rosenkranz MA: Field trial of live attenuated influenza A/B (“Alice”/R-75) vaccine. Am J Epidemiol. 1977, 105: 49-55.
Monto AS, Miller FD, Maassab HF: Evaluation of an attenuated, cold-recombinant influenza B virus vaccine. J Infect Dis. 1982, 145: 57-64. 10.1093/infdis/145.1.57.
Tannock GA, Bryce DA, Hensley MJ, Saunders NA, Gillett RS, Kennedy WS: Responses to one or two doses of a deoxycholate subunit influenza vaccine in a primed population. Vaccine. 1984, 2: 100-106. 10.1016/S0264-410X(98)90040-8.
Keitel WA, Cate TR, Couch RB, Huggins LL, Hess KR: Efficacy of repeated annual immunization with inactivated influenza virus vaccines over a five year period. Vaccine. 1997, 15: 1114-1122. 10.1016/S0264-410X(97)00003-0.
Gruber WC, Taber LH, Glezen WP, Clover RD, Abell TD, Demmler RW, Couch RB: Live attenuated and inactivated influenza vaccine in school-age children. Am J Dis Child. 1990, 144: 595-600.
Edwards KM, Dupont WD, Westrich MK, Plummer WD, Palmer PS, Wright PF: A randomized controlled trial of cold-adapted and inactivated vaccines for the prevention of influenza A disease. J Infect Dis. 1994, 169: 68-76. 10.1093/infdis/169.1.68.
Clover RD, Crawford S, Glezen WP, Taber LH, Matson CC, Couch RB: Comparison of heterotypic protection against influenza A/Taiwan/86 (H1N1) by attenuated and inactivated vaccines to A/Chile/83-like viruses. J Infect Dis. 1991, 163: 300-304. 10.1093/infdis/163.2.300.
Govaert TM, Thijs CT, Masurel N, Sprenger MJ, Dinant GJ, Knottnerus JA: The efficacy of influenza vaccination in elderly individuals. A randomized double-blind placebo-controlled trial. JAMA. 1994, 272: 1661-1665. 10.1001/jama.1994.03520210045030.
Powers DC, Smith GE, Anderson EL, Kennedy DJ, Hackett CS, Wilkinson BE, Volvovitz F, Belshe RB, Treanor JJ: Influenza A virus vaccines containing purified recombinant H3 hemagglutinin are well tolerated and induce protective immune responses in healthy adults. J Infect Dis. 1995, 171: 1595-1599. 10.1093/infdis/171.6.1595.
Belshe RB, Mendelman PM, Treanor J, King J, Gruber WC, Piedra P, Bernstein DI, Hayden FG, Kotloff K, Zangwill K, Iacuzio D, Wolff M: The efficacy of live attenuated, cold-adapted, trivalent, intranasal influenzavirus vaccine in children. N Engl J Med. 1998, 338: 1405-1412. 10.1056/NEJM199805143382002.
Rudenko LG, Arden NH, Grigorieva E, Naychin A, Rekstin A, Klimov AI, Donina S, Desheva J, Holman RC, DeGuzman A, Cox NJ, Katz JM: Immunogenicity and efficacy of Russian live attenuated and US inactivated influenza vaccines used alone and in combination in nursing home residents. Vaccine. 2001, 19: 308-318.
Belshe RB, Gruber WC, Mendelman PM, Cho I, Reisinger K, Block SL, Wittes J, Iacuzio D, Piedra P, Treanor J, King J, Kotloff K, Bernstein DI, Hayden FG, Zangwill K, Yan L, Wolff M: Efficacy of vaccination with live attenuated, cold-adapted, trivalent, intranasal influenza virus vaccine against a variant (A/Sydney) not contained in the vaccine. J Pediatr. 2000, 136: 168-175. 10.1016/S0022-3476(00)70097-7.
Bridges CB, Thompson WW, Meltzer MI, Reeve GR, Talamonti WJ, Cox NJ, Lilac HA, Hall H, Klimov A, Fukuda K: Effectiveness and cost-benefit of influenza vaccination of healthy working adults: a randomized controlled trial. JAMA. 2000, 284: 1655-1663. 10.1001/jama.284.13.1655.
Hoberman A, Greenberg DP, Paradise JL, Rockette HE, Lave JR, Kearney DH, Colborn DK, Kurs-Lasky M, Haralam MA, Byers CJ, Zoffel LM, Fabian IA, Bernard BS, Kerr JD: Effectiveness of inactivated influenza vaccine in preventing acute otitis media in young children: a randomized controlled trial. JAMA. 2003, 290: 1608-1616. 10.1001/jama.290.12.1608.
Tam JS, Capeding MR, Lum LC, Chotpitayasunondh T, Jiang Z, Huang LM, Lee BW, Qian Y, Samakoses R, Lolekha S, Rajamohanan KP, Narayanan SN, Kirubakaran C, Rappaport R, Razmpour A, Gruber WC, Forrest BD, Pan-Asian CAIV-T Pediatric Efficacy Trial Network: Efficacy and safety of a live attenuated, cold-adapted influenza vaccine, trivalent against culture-confirmed influenza in young children in Asia. Pediatr Infect Dis J. 2007, 26: 619-628. 10.1097/INF.0b013e31806166f8.
Vesikari T, Fleming DM, Aristegui JF, Vertruyen A, Ashkenazi S, Rappaport R, Skinner J, Saville MK, Gruber WC, Forrest BD: Safety, efficacy, and effectiveness of cold-adapted influenza vaccine-trivalent against community-acquired, culture-confirmed influenza in young children attending day care. Pediatrics. 2006, 118: 2298-2312. 10.1542/peds.2006-0725.
Forrest BD, Pride MW, Dunning AJ, Capeding MR, Chotpitayasunondh T, Tam JS, Rappaport R, Eldridge JH, Gruber WC: Correlation of cellular immune responses with protection against culture-confirmed influenza virus in young children. Clin Vaccine Immunol. 2008, 15: 1042-1053. 10.1128/CVI.00397-07.
Lum LC, Borja-Tabora CF, Breiman RF, Vesikari T, Sablan BP, Chay OM, Tantracheewathorn T, Schmitt HJ, Lau YL, Bowonkiratikachorn P, Tam JS, Lee BW, Tan KK, Pejcz J, Cha S, Gutierrez-Brito M, Kaltenis P, Vertruyen A, Czajka H, Bojarskas J, Brooks WA, Cheng SM, Rappaport R, Baker S, Gruber WC, Forrest BD: Influenza vaccine concurrently administered with a combination measles, mumps, and rubella vaccine to young children. Vaccine. 2010, 28: 1566-1574. 10.1016/j.vaccine.2009.11.054.
Langley JM, Aoki F, Ward BJ, McGeer A, Angel JB, Stiver G, Gorfinkel I, Shu D, White L, Lasko B, Dzongowski P, Papp K, Alexander M, Boivin G, Fries L: A nasally administered trivalent inactivated influenza vaccine is well tolerated, stimulates both mucosal and systemic immunity, and potentially protects against influenza illness. Vaccine. 2011, 29: 1921-1928. 10.1016/j.vaccine.2010.12.100.
Beran J, Wertzova V, Honegr K, Kaliskova E, Havlickova M, Havlik J, Jirincova H, Van Belle P, Jain V, Innis B, Devaster JM: Challenge of conducting a placebo-controlled randomized efficacy study for influenza vaccine in a season with low attack rate and a mismatched vaccine B strain: a concrete example. BMC Infect Dis. 2009, 9: 2-10.1186/1471-2334-9-2.
Beran J, Vesikari T, Wertzova V, Karvonen A, Honegr K, Lindblad N, Van Belle P, Peeters M, Innis BL, Devaster JM: Efficacy of inactivated split-virus influenza vaccine against culture-confirmed influenza in healthy adults: a prospective, randomized, placebo-controlled trial. J Infect Dis. 2009, 200: 1861-1869. 10.1086/648406.
Frey S, Vesikari T, Szymczakiewicz-Multanowska A, Lattanzi M, Izu A, Groth N, Holmes S: Clinical efficacy of cell culture-derived and egg-derived inactivated subunit influenza vaccines in healthy adults. Clinical Infect Dis. 2010, 51: 997-1004. 10.1086/656578.
Treanor JJ, El Sahly H, King J, Graham I, Izikson R, Kohberger R, Patriarca P, Cox M: Protective efficacy of a trivalent recombinant hemagglutinin protein vaccine (FluBlok(R)) against influenza in healthy adults: a randomized, placebo-controlled trial. Vaccine. 2011, 29: 7733-7739. 10.1016/j.vaccine.2011.07.128.
Barrett PN, Berezuk G, Fritsch S, Aichinger G, Hart MK, El-Amin W, Kistner O, Ehrlich HJ: Efficacy, safety, and immunogenicity of a Vero-cell-culture-derived trivalent influenza vaccine: a multicentre, double-blind, randomised, placebo-controlled trial. Lancet. 2011, 377: 751-759. 10.1016/S0140-6736(10)62228-3.
Cowling BJ, Ng S, Ma ES, Cheng CK, Wai W, Fang VJ, Chan KH, Ip DK, Chiu SS, Peiris JS, Leung GM: Protective efficacy of seasonal influenza vaccination against seasonal and pandemic influenza virus infection during 2009 in Hong Kong. Clinical Infect Dis. 2010, 51: 1370-1379. 10.1086/657311.
Talaat KR, Greenberg ME, Lai MH, Hartel GF, Wichems CH, Rockman S, Jeanfreau RJ, Ghosh MR, Kabongo ML, Gittleson C, Karron RA: A single dose of unadjuvanted novel 2009 H1N1 vaccine is immunogenic and well tolerated in young and elderly adults. J Infect Dis. 2010, 202: 1327-1337. 10.1086/656601.
Keitel WA, Cate TR, Couch RB: Efficacy of sequential annual vaccination with inactivated influenza virus vaccine. Am J Epidemiol. 1988, 127: 353-364.
Kelly HA, Sullivan SG, Grant KA, Fielding JE: Moderate influenza vaccine effectiveness with variable effectiveness by match between circulating and vaccine strains in Australian adults aged 20–64 years, 2007–2011. Influenza Other Respi Viruses. in press
Landry ML: Diagnostic tests for influenza infection. Curr Opin Pediatr. 2011, 23: 91-97. 10.1097/MOP.0b013e328341ebd9.
Petrie JG, Ohmit SE, Johnson E, Cross RT, Monto AS: Efficacy studies of influenza vaccines: effect of end points used and characteristics of vaccine failures. J Infect Dis. 2011, 203: 1309-1315. 10.1093/infdis/jir015.
Schulz KF, Altman DG, Moher D: CONSORT 2010 Statement: Updated guidelines for reporting parallel group randomised trials. J Clin Epidemiol. 2010, 63: 834-840. 10.1016/j.jclinepi.2010.02.005.
Smith DJ, Lapedes AS, de Jong JC, Bestebroer TM, Rimmelzwaan GF, Osterhaus AD, Fouchier RA: Mapping the antigenic and genetic evolution of influenza virus. Science. 2004, 305: 371-376. 10.1126/science.1097211.
Skowronski DM, Janjua NZ, De Serres G, Winter AL, Dickinson JA, Gardy JL, Gubbay J, Fonseca K, Charest H, Crowcroft NS, Fradet MD, Bastien N, Li Y, Krajden M, Sabaiduc S, Petric M: A sentinel platform to evaluate influenza vaccine effectiveness and new variant circulation, Canada 2010–2011 season. Clinical Infect Dis. 2012, 55: 332-342. 10.1093/cid/cis431.
Belshe RB, Coelingh K, Ambrose CS, Woo JC, Wu X: Efficacy of live attenuated influenza vaccine in children against influenza B viruses by lineage and antigenic similarity. Vaccine. 2012, 28: 2149-2156.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1741-7015/11/153/prepub
We thank Laure Perrier for updating the literature searches, Bruno Kovic for retrieving some of the articles, and Dr Sharon E. Straus for providing feedback on the draft manuscript. We also thank Drs. William Gruber, Suzanne Ohmit, Arnold Monto, and Lisa Jackson for sharing their unpublished data with us. ACT is funded by a Canadian Institutes for Health Research/Drug Safety and Effectiveness Network New Investigator Award in Knowledge Synthesis.
ACT, DH, MT, CTB, and ML have received consulting fees from GlaxoSmithKline. CTB has received a grant from GlaxoSmithKline. St Michael's Hospital received a grant to conduct this research. ACT and ML have received financial support for travel to meetings. AC and GM are paid employees of GlaxoSmithKline and also own company stock. CS has nothing to declare. This systematic review was funded by GlaxoSmithKline, Canada. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
ACT conceived the study, designed the study, screened citations and full text articles, abstracted the data, analyzed the data, interpreted the data, and wrote the manuscript. AC conceived the study and edited the manuscript. CS screened citations and full text articles, abstracted the data, generated tables, and edited the manuscript. DH screened citations and full text articles and edited the manuscript. GM conceived the study and edited the manuscript. MHC conducted the statistical analysis, interpreted the data and edited the manuscript. MK screened citations and full text articles and edited the manuscript. CB conceived the study and edited the manuscript. ML conceived the study, designed the study, interpreted the data and edited the manuscript. All authors have read and approved the final manuscript.
Authors’ original submitted files for images
About this article
Cite this article
Tricco, A.C., Chit, A., Soobiah, C. et al. Comparing influenza vaccine efficacy against mismatched and matched strains: a systematic review and meta-analysis. BMC Med 11, 153 (2013). https://0-doi-org.brum.beds.ac.uk/10.1186/1741-7015-11-153
- Antigenic variation
- Cross protection
- Influenza A virus
- Influenza B virus
- Systematic review