Alberto Tozzi · Humoral and B-cell memory responses in children five years after pertussis acellular vaccine priming
Article1 min read·Published Feb 2014Older

Humoral and B-cell memory responses in children five years after pertussis acellular vaccine priming

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Article · Feb 2014 · 1 min read

In brief

In brief

Five-year follow-up study comparing immune persistence after primary vaccination with two acellular pertussis vaccines (Hexavac vs Infanrix) in children. Both vaccines induced similar B-cell memory responses, with over 80% maintaining positive memory responses, though only 50% retained protective antibody levels without booster—emphasizing the importance of pre-school booster doses for sustained protection.

Written by the GCMD Library team from the article.

Alberto Tozzi

The resurgence of pertussis suggests the need for greater efforts in understanding the long-lasting protective responses induced by vaccination. In this paper we dissect the persistence of humoral and B-cell memory responses induced by primary vaccination with two different acellular pertussis (aP) vaccines, hexavalent Hexavac(®) vaccine (Hexavac) (Sanofi Pasteur MSD) and Infanrix hexa(®) (Infanrix) (GlaxoSmithKline Biologicals). We evaluated the specific immune responses in the two groups of children, 5 years after primary vaccination by measuring the persistence of IgG and antibody secreting cells (ASC) specific for vaccine antigens. Part of the enrolled children received only primary vaccination, while others had the pre-school boost dose. A similar level of antigen-specific IgG and ASC was found in Infanrix and Hexavac vaccinated children. The mean IgG levels were significantly higher in children that received the pre-school boost as compared with children that did not receive the boost dose. A longer persistence after the pre-school boost of IgG-Pertussis Toxin (PT) and IgG-pertactin levels was observed in Infanrix primed children, but it was not statistically significant. More than 80% of children presented a positive ASC B memory response. Around 50% of children still presented protective IgG-PT levels which are reduced to 36% in no-boosted children. The pre-school booster dose restores the percentage of protected children above 50%. In conclusion our data underline th

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