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Published on: August 11, 2018
Pertussis-specific cell-mediated immunity in infants after vaccination with a tricomponent acellular pertussis
1Pediatric Immunology and Infectious Diseases, Children's Hospital, Johannes Gutenberg University of Mainz, Germany. zepp@mzdmza.zdv.uni-mainz.de
Insights
This study shows that infant pertussis vaccination with a tricomponent acellular vaccine generates lasting cell-mediated immunity. These T-cell responses remain stable, unlike antibody levels, suggesting a role in sustained protection.
Area of Science:
- Immunology
- Vaccinology
- Pediatric Infectious Diseases
Background:
- Pertussis (whooping cough) remains a concern despite vaccination.
- Understanding cell-mediated immunity post-vaccination is crucial for assessing protection duration.
- Acellular pertussis vaccines are widely used, necessitating research into their immunological impact.
Purpose of the Study:
- To investigate pertussis-specific cell-mediated immunity in infants receiving a tricomponent acellular vaccine.
- To analyze immune responses during primary vaccination and after a booster dose.
- To characterize T-cell responses and cytokine profiles in infants under 12 months.
Main Methods:
- Infants were monitored during primary vaccination (3-6 months) and pre/post-booster (15-24 months).
- T-cell responses to vaccine antigens (detoxified pertussis toxin, filamentous hemagglutinin, pertactin) were assessed.
- Activation marker expression (CD45RO) and cytokine secretion (IL-2, IFN-γ, IL-10) were measured.
Main Results:
- The vaccine induced progressive T-cell responses specific to pertussis antigens.
- Cell-mediated immunity remained stable between primary vaccination and booster doses, contrasting with declining antibody titers.
- Vaccination increased CD45RO+ T cells and promoted a T-helper 1 cytokine profile (IL-2, IFN-γ).
Conclusions:
- Tricomponent acellular pertussis vaccines induce persistent cell-mediated immunity in infants.
- Stable cell-mediated immune responses may contribute to the protective mechanisms of pertussis vaccination.
- Further research is needed to understand the persistence of cell-mediated immunity and its role in vaccine efficacy over time.
Abstract:
The aim of this study was to investigate pertussis-specific cell-mediated immunity in infants vaccinated with a tricomponent acellular vaccine. Infants were investigated during a primary vaccination schedule from the third month of life to the sixth month as well as before and after a booster at 15 to 24 months. This is the first report of specific cell-mediated immune responses to pertussis-related antigens in infants below the age of 12 months. Our data show that the vaccine induces T-cell responses specific for the vaccine components, detoxified pertussis toxin, filamentous hemagglutinin, and pertactin, that increase progressively over the course of the vaccination schedule. In contrast to declining antibody titers, cell-mediated immune responses are stable over the postprimary to prebooster period. Vaccination results in a progressive increase in the number of T cells that express activation marker CD45RO preferentially on CD4-positive T cells after stimulation with pertussis antigens. Measurements of cytokine secretion profiles demonstrated a preferential induction of interleukin 2- and gamma interferon-producing T-helper 1 cells and only low production of interleukin 10. The observed persistence of the specific cell-mediated immunity may have a bearing on the protective mechanisms induced by pertussis vaccination. Cell-mediated immunity requires further study, particularly to improve our understanding of the persistence of protection afforded by vaccination up to the administration of booster doses.
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