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Clinical Trial
. 2012 Mar;119(3):631-9.
doi: 10.1097/AOG.0b013e318244ed20.

Immunogenicity of trivalent inactivated influenza vaccination received during pregnancy or postpartum

Affiliations
Clinical Trial

Immunogenicity of trivalent inactivated influenza vaccination received during pregnancy or postpartum

Rhoda S Sperling et al. Obstet Gynecol. 2012 Mar.

Abstract

Objective: To estimate the effects of gestational age and other maternal factors on immunologic responses to influenza vaccination.

Methods: Antepartum and postpartum women receiving influenza vaccination as part of routine clinical care were enrolled through four consecutive vaccination seasons (starting October 2006 through January 2010). Immunologic responses to trivalent inactivated influenza vaccine and monovalent H1N1 were assessed as well as factors influencing vaccine responsiveness. Serum samples were obtained at baseline and 4-8 weeks postvaccination.

Results: Two hundred thirty-nine participants were included in the current analysis. Seroconversion rates to trivalent inactivated influenza vaccine strains were lowest in the first trimester (54.8%) and immediately postpartum (54.8%) and were highest in the late third trimester (69.6%) and late postpartum (69.4%); these differences were not statistically significant (P=.23). In a multivariable model, higher baseline antibody levels (P<.001) and prior year flu vaccination (P=.03) were both significantly associated with reduced odds of seroconversion. Overall, results were consistent when comparing trivalent inactivated influenza vaccine and monovalent pandemic H1N1 responses. Although there was overall no significant association between gestational age at vaccination (P=.23) or prepregnancy body mass index (P=.16), we observed somewhat lower rates of seroconversion for women vaccinated in the first trimester and for obese women.

Conclusion: Adequate immunologic responses to inactivated influenza vaccines were demonstrated during pregnancy and the postpartum period. No diminution of immunogenicity was observed in the third trimester, a time of increased clinical vulnerability to influenza.

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Conflict of interest statement

Financial Disclosure The authors did not report any potential conflicts of interest.

Figures

Figure 1
Figure 1
Seroprotection rates for Influenza A(H3N2 strains).
Figure 2
Figure 2
Seroprotection rates for Influenza A (H1N1 strains).

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