4.5 Article

Comparing live attenuated and inactivated hepatitis A vaccines: An immunogenicity study after one single dose

Journal

VACCINE
Volume 29, Issue 48, Pages 9098-9103

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.vaccine.2011.08.078

Keywords

Immunogenicity; Hepatitis A vaccine

Funding

  1. Ministry of Health and National of Science and Technology [2008BAI56B00]

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Introduction: While three types of hepatitis A vaccines are available in China, little data are available to compare them in terms of early antibody response. We conducted a trial to compare antibody response at 7, 14 and 28 days. Methods: We randomized primary school children in Gansu and Jilin provinces into four groups to receive either (1) Chinese live attenuated hepatitis A vaccine (H2 strain), (2) domestic inactivated hepatitis A vaccine (Healive (R)), (3) imported inactivated hepatitis A vaccine (Havrix (R)) or (4) hepatitis B vaccine (Control group). We compared groups at 7, 14 and 28 days in terms of proportion of sero-conversions (>= 10 mUl/ml), and Geometric Mean Concentration (GMC) of antibodies measured with a Microparticle Enzyme Immunoassay (MEIA). We compared rates of self-reported adverse events following immunization (AEFI) in the first three days. Results: 204 children received the H2 vaccine, 208 received Healive (R), 214 received Havrix (R), and 215 received hepatitis B vaccine (no differences across groups in terms of age, sex, weight and height). At seven days, sero-conversion proportions were 25%, 35%, 27% and 2% (p < 0.0001) with GMC of 6 mIU/ml, 8 mIU/ml, 6 mIU/ml and 3 mIU/ml, respectively for the four groups. At 28 days, sero-conversion proportions were 98%, 100%, 93% and 3% (p < 0.0001) with GMC of 47 mIU/ml, 71 mIU/ml, 67 mIU/ml and 3 mIU/ml, respectively. AEFI were benign and did not differ across groups (p = 0.94). Conclusions: While our study was not able to identify differences between Havrix (R), Healive (R) and H2 vaccine in terms of sero-conversion proportion and GMC between seven and 28 days, further studies should evaluate non-inferiority or equivalence of the Chinese vaccines, particularly with respect to the GMC concentration for the H2 vaccine since it could affect long-term protection. (C) 2011 Elsevier Ltd. All rights reserved.

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