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Primary immunization series for infants: comparison of two-component acellular and standard whole-cell pertussis
S Feldman1, C S Perry, M Andrew
1Department of Pediatrics, University of Mississippi Medical Center, Jackson 39216.
Insights
A new two-component acellular pertussis vaccine demonstrated fewer adverse reactions and improved antibody responses compared to the standard whole-cell pertussis vaccine in infants. This acellular vaccine offers a potentially safer and more effective immunization option.
Area of Science:
- Pediatric Vaccinology
- Immunology
- Public Health
Background:
- Pertussis remains a significant public health concern, necessitating effective vaccination strategies.
- Current whole-cell pertussis vaccines can be associated with notable adverse reactions.
- Development of acellular pertussis vaccines aims to improve safety profiles while maintaining immunogenicity.
Purpose of the Study:
- To compare the safety and immunogenicity of a two-component acellular pertussis vaccine against a standard whole-cell pertussis vaccine in infants.
- To evaluate local and systemic adverse reactions following primary immunization.
- To assess antibody responses to key pertussis antigens, lymphocytosis-promoting factor (LPF) and filamentous hemagglutinin (FHA).
Main Methods:
- A randomized controlled trial involving 145 infants at 2 months of age.
- Infants received either a two-component acellular pertussis vaccine (LPF/FHA) or a standard whole-cell pertussis vaccine, combined with diphtheria-tetanus toxoids.
- Adverse reactions, acetaminophen usage, and antibody titers to LPF and FHA were monitored throughout the primary immunization series.
Main Results:
- The acellular pertussis vaccine group experienced significantly fewer local (5% vs. 30%) and systemic (17% vs. 30%) adverse reactions.
- A higher percentage of acellular vaccine doses were reaction-free (35% vs. 12%) compared to whole-cell doses.
- Antibody responses to LPF and FHA were significantly higher and consistently elevated after the second and third immunizations with the acellular vaccine.
Conclusions:
- The two-component acellular pertussis vaccine is associated with a superior safety profile, characterized by reduced adverse reactions.
- The acellular vaccine elicits improved and sustained serologic responses to LPF and FHA antigens.
- This acellular pertussis vaccine represents a promising alternative to the currently recommended whole-cell vaccine for infant immunization.
Abstract:
At 2 months of age, 145 infants were randomized to receive either a two-component acellular pertussis vaccine [lymphocytosis-promoting factor (LPF)/filamentous hemagglutinin (FHA)] or standard whole-cell pertussis vaccine, each combined with diphtheria-tetanus toxoids, as their primary immunization series. Of the 132 subjects (91%) who completed the study, those receiving the acellular vaccine had significantly fewer adverse reactions: 5% vs 30% (local) and 17% vs 30% (systemic, including fever). During the first 24 hours acetaminophen usage, a general measure of adverse reactions, was lower in the test group. Overall, 35% of the acellular vaccine doses were reaction free vs 12% of the whole-cell doses. No serious reactions occurred in either group. Antibody responses to LPF and to FHA were significantly increased after the second and third immunizations with the test vaccine and were consistently higher than levels achieved with the standard vaccine. Thus the two-component acellular pertussis vaccine was associated with fewer adverse reactions and improved serologic responses to LPF and FHA as compared with the currently recommended whole-cell vaccine.
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