Immunogenicity and Safety of a Booster Injection of DTap-IPV//Hib (Pentaxim) Administered Concomitantly With Tetravalent Dengue Vaccine in Healthy Toddlers 15-18 Months of Age in Mexico

被引:9
作者
Rodriguez Melo, Flor Irene [1 ]
Renteria Morales, Jose Juan [2 ]
Mascarenas De Los Santos, Abiel Homero [3 ,4 ]
Rivas, Enrique [5 ]
Vigne, Claire [6 ]
Noriega, Fernando [7 ]
机构
[1] Hosp Ctr Especialidades Med Sureste, BIOCEM Unidad Invest Biomed, Merida, Yucatan, Mexico
[2] Ctr Invest Clin Pacifico, Acapulco, Guerreo, Mexico
[3] Univ Autonoma Nuevo Leon, Serv Med, San Nicolos De Los Garza, NL, Mexico
[4] Univ Autonoma Nuevo Leon, Ctr Invest & Desarrollo Ciencias Salud, San Nicolos De Los Garza, NL, Mexico
[5] Sanofi Pasteur, Clin Sci, Ave Univ 1738, Mexico City 04000, DF, Mexico
[6] Sanofi Pasteur, Clin Program, Marcy Letoile, France
[7] Sanofi Pasteur, Clin Sci, Swiftwater, PA USA
关键词
dengue; DTaP-IPV//Hib vaccine; safety; immunogenicity; toddlers; TO-T VACCINE; LATIN-AMERICA; CHILDREN; ANTIBODIES; EFFICACY; VIRUSES; TRIAL; PERU;
D O I
10.1097/INF.0000000000001542
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The live, attenuated, tetravalent dengue vaccine (CYD-TDV) is licensed in a number of dengue endemic countries for individuals >= 9 years of age. Before the integration of any vaccine into childhood vaccination schedules, a lack of immune interference and acceptable safety when coadministered with other recommended vaccines should be demonstrated. Methods: This randomized, multi-center phase III trial was conducted in Mexico. Healthy toddlers (n = 732) received a booster dose of a licensed pentavalent combination vaccine [diphtheria, tetanus, acellular pertussis, inactivated polio vaccine and Haemophilus influenzae type b (DTaP-IPV//Hib)] either concomitantly or sequentially, with the second dose of CYD-TDV administered as a 3-dose schedule. Antibody titers against diphtheria toxoid, tetanus toxoid and pertussis antigens were measured by enzyme-linked immunosorbent assay. Antibodies against poliovirus and dengue serotypes were measured using a plaque reduction neutralization test. Non-inferiority was demonstrated for each of the DTaP-IPV//Hib antigens if the lower limit of the 2-sided 95% confidence interval of the difference in sero-conversion rates between the 2 groups (CYD-TDV and placebo) was >= 10%. Safety of both vaccines was assessed. Results: Noninferiority in immune response was demonstrated for all DTaP-IPV//Hib antigens. After 3 doses of CYD-TDV, no difference was observed in the immune response for CYD-TDV between groups. There were no safety concerns during the study. Conclusion: Coadministration of the DTaP-IPV//Hib booster vaccine with CYD-TDV has no observed impact on the immunogenicity or safety profile of the DTaP-IPV//Hib booster vaccine. No difference was observed on the CYD-TDV profile when administered concomitantly or sequentially with the DTaP-IPV//Hib booster vaccine.
引用
收藏
页码:602 / 608
页数:7
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