Immunogenicity and reactogenicity of primary immunization with a novel combined haemophilus influenzae type b and Neisseria meningitidis serogroup C-tetanus toxoid conjugate vaccine coadministered with a diphtheria-tetanus-acellular pertussis-hepatitis B-inactivated poliovirus vaccine at 2, 4 and 6 months

被引:19
|
作者
Tejedor, Juan C.
Moro, Manuel
Ruiz-Contreras, Jesus
Castro, Javier
Gomez-Campdera, Jose Antonio
Navarro, Maria Luisa
Merino, Jose Manuel
Martin-Ancel, Ana
Roca, Joan
Garcia-del-Ri, Manuel
Jurado, Antonio
Diez-Delgado, Francisco Javier
Omenaca, Felix
Garcia-Sicilia, Jose
Boceta, Reyes
Garcia-Corbeira, Pilar
Collard, Alix
Boutriau, Dominique
Schuerman, Lode
Jacquet, Jeanne-Marie
机构
[1] Mostoles Hosp, Madrid, Spain
[2] Clin San Carlos Hosp, Madrid, Spain
[3] Octibre Hosp 12, Madrid, Spain
[4] Gregorio Maranon Hosp, Madrid, Spain
[5] Gen Yague Hosp, Burgos, Spain
[6] Alcorcon Hosp, Madrid, Spain
[7] Sant Joan De Deu Hosp, Barcelona, Spain
[8] Carlos Haya Hosp, Malaga, Spain
[9] Torrecardenas Hosp, Almeria, Spain
[10] GlaxoSmithKline, Dept Med, Madrid 28760, Spain
[11] Hosp La Paz, Madrid, Spain
关键词
Haemophilus influenzae type b conjugate vaccine; meningococcal C conjugate vaccine; DTPa-HBV-IPV vaccine; primary immunization; coadministration;
D O I
10.1097/01.inf.0000247070.60063.09
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: This phase II study evaluated the immunogenicity and reactogenicity of primary vaccination with a novel Hib-MenC conjugate vaccine (GlaxoSmithKline [GSK] Biologicals) coadministered with DTPa-HBV-IPV (GSK Biologicals) at 2, 4 and 6 months. Methods: Healthy infants were randomized to receive Hib-MenC coadministered with DTPa-HBV-IPV (N = 117) or MenC-CRM (Wyeth) coadministered with DTPa-HBV-IPV/Hib (GSK Biologicals; N = 120) at 2, 4 and 6 months. Antibody concentrations were measured before vaccination and after doses 2 and 3. Solicited local and general symptoms, unsolicited symptoms and serious adverse events (SAEs) were recorded. Results: All subjects in the Hib-MenC group had seroprotective titers of anti-PRP antibodies (>= 0.15 mu g/mL) and SBA-MenC titers (>= 1:8) 1 month after the third dose. These responses were noninferior to those seen in the control group, in which a 99.1% scroprotection rate was observed for both Hib and MenC. At that time, anti-PRP and SBA-MenC GMTs were significantly higher in the Hib-MenC group (12.8 mu g/mL and 2467.1 mu g/mL, respectively) than in the control group (3.8 mu g/mL and 1833.7 mu g/mL). High seroprotection rates were already observed after the second dose of Hib-MenC; 96.4% and 100% of subjects were seroprotected to Hib and MenC, respectively. Immune responses to coadministered antigens were unimpaired; seroprotection/vaccine response rates >= 96.5% were recorded postdose 3 in the Hib-MenC group. No differences in reactogenicity were seen between the 2 study groups. Conclusions: Coadministration of a Hib-MenC conjugate vaccine with DTPa-HBV-IPV is well tolerated and immunogenic, and does not impair the immune response to any of the coadministered antigens.
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页码:1 / 7
页数:7
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