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Clinical Reactions and Immunogenicity of the BIKEN Acellular Diphtheria and Tetanus Toxoids and Pertussis Vaccine in 4- Through 6-Year-Old US Children

Henry H. Bernstein, DO; Edward P. Rothstein, MD; Michael E. Pichichero, MD; Anne B. Francis, MD; Arthur J. Kovel, MD; Frank A. Disney, MD; John L. Green, MD; Steven M. Marsocci, MD; A. Marie Lynd, MD; Gordon C. Wood, MD; Ruth P. Schiller, MD; Joseph A. C. Girone, MD; Thomas J. Hipp, MD; Ronald L. Souder, MD; Thomas I. Kennedy, MD; Carlton K. Meschievitz, MD
Am J Dis Child. 1992;146(5):556-559. doi:10.1001/archpedi.1992.02160170036012.
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• Objective.  —To compare the immunogenicity and reactogenicity of a two-component acellular pertussis vaccine with a whole-cell diphtheria and tetanus toxoids and pertussis vaccine (W-DTP) when administered as a booster to children 4 through 6 years of age.

Design.  —This was a randomized, double-blind study.

Setting.  —Children in this study were from three general pediatric practices (two were private, one was university-affiliated).

Participants.  —Three hundred and sixteen 4- through 6-year-old children who had received four previous W-DTP immunizations at the recommended times were studied.

Selection Procedures and Interventions.  —Children were randomly assigned in a 1:3 ratio to receive either W-DTP or one of three lots of acellular diphtheria and tetanus toxoids and pertussis vaccine (A-DTP). The A-DTPs contained 3.75 μg each of lymphocytosis promoting factor and filamentous hemagglutinin protein nitrogen per 0.5 mL and the same concentrations of diphtheria and tetanus toxoids as W-DTP. Serum samples were obtained on the day of immunization and 4 to 6 weeks later. Adverse reactions were recorded by parents at 6, 24, 48, and 72 hours.

Measurements and Results.  —An indirect enzyme-linked immunosorbent assay (ELISA) method determined IgG antibody response to lymphocytosis promoting factor, filamentous hemagglutinin, and tetanus toxoid; a CHO cell assay measured neutralizing antibodies to pertussis toxin; and serum neutralization on VERO cells assayed diphtheria antitoxin. One month after booster doses were administered, the geometric mean antibody levels for A-DTP vs W-DTP were IgG filamentous hemagglutinin, 408 vs 81 ELISA U/mL; IgG lymphocytosis promoting factor, 362 vs 104 ELISA U/mL; CHO cell, 210 vs 107; diphtheria, 21.7 vs 12.1 U/mL;, and tetanus, 2.86 vs 2.04 Eq/mL. Following immunization with A-DTP, local and systemic adverse experiences were 30% to 50% and 20% to 30% fewer, respectively, as compared with W-DTP.

Conclusions.  —The BIKEN A-DTP vaccine used in this study demonstrates enhanced immunogenicity to lymphocytosis promoting factor, filamentous hemagglutinin, and other measured antigens and less reactogenicity compared with licensed W-DTP.(AJDC. 1992;146:556-559)

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