학술논문

Immunology of combining CRM.sub.197 conjugates for Streptococcus pneumoniae, Neisseria meningitis and Haemophilus influenzae in Chilean infants
Document Type
Report
Source
Vaccine. April 14, 2009, Vol. 27 Issue 17, p2299, 7 p.
Subject
Customer relationship management
Hemophilus infections
Meningitis
Antigens
Infants
Antibodies
Viral antibodies
Bacterial pneumonia
Pneumonia
Customer relationship management
Language
English
ISSN
0264-410X
Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.vaccine.2009.02.022 Byline: Rosanna Lagos (a)(b), Alma Munoz (b), Myron M. Levine (c), Wendy Watson (d), Ih Chang (e), Peter Paradiso (f) Keywords: Pneumococcal conjugate vaccine; Immunogenicity; Combination vaccines Abstract: We evaluated the immunogenicity and safety of an investigational combination of 9-valent pneumococcal conjugate vaccine (PCV9) and meningococcal group C conjugate (MnCC) vaccine (PCV9-MnCC) administered concomitantly with Haemophilus influenzae type b (Hib) conjugate vaccine, and of a combination of the three vaccines mixed together as a single injection (Hib-PCV9-MnCC), and compared them to separately administered PCV9 and MnCC dispensed to Chilean infants at 2, 4, and 6 months of age. The frequency of adverse events was similar among groups. Recipients of PCV9 alone or in combination with the other vaccines mounted significant antibody responses to the nine pneumococcal serotypes in PCV9, with >88% achieving protective levels of [greater than or equal to]0.35[mu]g/mL. For serotypes 6B, 9V, and 5, recipients of PCV9 alone had significantly higher geometric mean concentrations (GMCs) than those of the other vaccine groups. Similarly, the GMC of anti-PRP antibodies was significantly lower among recipients of Hib-PCV9-MnCC than among those who received Hib vaccine separately from PCV9 or MnCC. In Chilean infants, PCV9, PCV9-MnCC, and Hib-PCV9-MnCC were highly immunogenic and safe. Overall, interactions of PCV9, MnCC and Hib affected the magnitude (GMC) of the primary antibody responses to some of the antigens, but not the percentage of subjects who achieved protective antibody thresholds. Author Affiliation: (a) Hospital de NiA[+ or -]os Roberto del Rio, Servicio de Salud Metropolitano Norte, Santiago, Chile (b) Centro para Vacunas en Desarrollo-Chile, Santiago, Chile (c) Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, United States (d) Wyeth Vaccine Research, Pearl River, NY, United States (e) Novartis Pharmaceuticals Corp, East Hanover, NJ, United States (f) Wyeth Pharmaceuticals, Collegeville, PA, United States Article History: Received 5 August 2008; Revised 3 February 2009; Accepted 4 February 2009