Abstract |
We compared an acellular (B type) pertussis-component diphtheria- tetanus- pertussis (DTP-Ac) vaccine containing equal amounts of filamentous hemagglutinin and lymphocytosis-promoting factor with a conventional whole-cell vaccine as the first booster immunization in 162 healthy children 15 to 24 months of age. Fewer local reactions (e.g., erythema, swelling, and tenderness at the injection site) were seen in DTP-Ac vaccine recipients during the first 48 hours of observation. This group also had fewer episodes of fever (> or = 38 degrees C) and other systemic reactions (e.g., irritability, drowsiness, and anorexia). Overall, 57% of the DTP-Ac vaccine recipients had no obvious adverse reactions, in contrast to 5% in the comparison group. At 4 to 8 weeks after vaccination, serum antibody responses to filamentous hemagglutinin and lymphocytosis-promoting factor were greater in recipients of the acellular vaccine as determined by an enzyme-linked immunosorbent assay. We conclude that this B-type acellular vaccine is both immunogenic and much less likely to cause an adverse reaction than a currently licensed whole-cell vaccine, and is suitable for routine booster immunizing doses to protect against pertussis.
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Authors | S Feldman, S Perry, M Andrew, L Jones, J E Moffitt |
Journal | The Journal of pediatrics
(J Pediatr)
Vol. 121
Issue 6
Pg. 857-61
(Dec 1992)
ISSN: 0022-3476 [Print] United States |
PMID | 1447645
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Bacterial
- Diphtheria-Tetanus-Pertussis Vaccine
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Topics |
- Analysis of Variance
- Antibodies, Bacterial
(blood)
- Bordetella pertussis
(immunology)
- Chi-Square Distribution
- Diphtheria-Tetanus-Pertussis Vaccine
(adverse effects, immunology)
- Double-Blind Method
- Enzyme-Linked Immunosorbent Assay
- Humans
- Immunization, Secondary
(statistics & numerical data)
- Infant
- Time Factors
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