An adolescent-adult formulation tetanus and diptheria toxoids adsorbed combined with acellular pertussis vaccine has comparable immunogenicity but less reactogenicity in children 4-6 years of age than a pediatric formulation acellular pertussis vaccine and diphtheria and tetanus toxoids adsorbed combined with inactivated poliomyelitis vaccine

被引:18
|
作者
Langley, Joanne A.
Predy, Gerald
Guasparini, R.
Law, Barbara
Diaz-Mitoma, Francisco
Whitstitt, Paul
Tapiero, Bruce
Dionne, Marc
Tomovici, A.
Mills, Elaine
Halperin, Scott A.
机构
[1] Dalhousie Univ, Clin Trials Res Ctr, Halifax, NS, Canada
[2] Dalhousie Univ, Dept Pediat, Halifax, NS B3H 3J5, Canada
[3] Dalhousie Univ, Dept Epidemiol & Community Hlth, Halifax, NS B3H 3J5, Canada
[4] Dalhousie Univ, Dept Immunol & Microbiol, Halifax, NS B3H 3J5, Canada
[5] Capital Hlth, Edmonton, AB, Canada
[6] Univ Manitoba, Winnipeg, MB R3T 2N2, Canada
[7] Childrens Hosp Eastern Ontario, Ottawa, ON, Canada
[8] Paradign Clin Trials, Ottawa, ON, Canada
[9] Univ Montreal, Montreal, PQ H3C 3J7, Canada
[10] Univ Quebec, Ctr Hosp, Beauport, PQ, Canada
[11] Sanofi Rech, Toronto, ON, Canada
关键词
adverse events; immunogenicity; vaccines; pertussis; diphtheria; tetanus; child;
D O I
10.1016/j.vaccine.2006.09.053
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In Canada. the fifth dose of the routine childhood immunization schedule against diphtheria, tetanus, pertussis and polio is given at 4-6 years of age. Up to 30% of children may have significant local reactions (redness, swelling) and this may be related to pertussis and diphtheria antigen content. We sought to determine if a combination product with lower content of pertussis and diphtheria toxoids (dTap) would result in fewer local reactions and not have inferior immunogenicity to a combination vaccine with higher pertussis and diphtheria content (diphthefia-tetanus-acellular pertussis-inactivated polio virus, DTaP-IPV). Healthy children aged 4-6 years with complete primary immunization series and a fourth dose of diphtheria and tetanus toxoids component pertussis inactivated polio and Haemophilus influenzae type B conjugate vaccine were randomized to one dose of dTap, followed in 4-6 weeks by one dose of IPV or control DTaP-IPV. Immediate reactions within 30 min, solicited injection site and systemic reactions within 14 days, and unsolicited adverse events (AE) within 6 weeks post-vaccination were monitored. Serum was collected prior to immunization, and 4-6 weeks after vaccine for diphtheria, tetanus and pertussis antibodies (Ab). Sample size was designed to detect >= 10% difference in injection site erythema, pain or swelling between groups 593 children at eight Canadian sites completed the study; no participant withdrew because of an AE. All safety endpoints on days 0-14 were less frequent in children randomized to the dTap than DTaP-IPV group: erythema (34.6% versus 51.7%), swelling (24.2% versus 33.8%) and pain (39.6% versus 67.2%). Fever was also less common (8.72% versus 16.9%). All children in both study groups had seroprotective Ab levels to diphtheria and tetanus at 4-6 weeks (>= 0.10 IU/mL). The majority of children in each vaccine arm had a four-fold increase in pertussis antibodies. Fever and injection site reactions are less common in 4-6 year-old-children who receive a dTap vaccine compared to DTaP-IPV, without inferior immunogenicity. (c) 2006 Elsevier Ltd. All rights reserved.
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页码:1121 / 1125
页数:5
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