PMID- 10192710 OWN - NLM STAT- MEDLINE DCOM- 19990504 LR - 20190831 IS - 0934-9723 (Print) IS - 0934-9723 (Linking) VI - 18 IP - 1 DP - 1999 Jan TI - Randomised study of the possible adjuvant effect of BCG vaccine on the immunogenicity of diphtheria-tetanus-acellular pertussis vaccine in Senegalese infants. PG - 23-9 AB - Following a study in Senegal (1990-1995) in which the relative efficacy of a diphtheria-tetanus-acellular pertussis vaccine (DTaP) was compared with that of a diphtheria-tetanus-whole-cell pertussis vaccine in children given a simultaneous injection of Bacille Calmette-Guerin (BCG) vaccine, this subsequent study was conducted to evaluate the possible adjuvant effect of the BCG vaccine on acellular pertussis vaccine components. A second objective was to compare the immunogenicity of these components when administered in accordance with a 2-4-6-month (spaced) schedule or an accelerated 2-3-4-month schedule. In all, 390 healthy Senegalese infants were randomly divided into three groups of 130 infants. Antibodies to acellular pertussis components were measured in serum samples obtained within 2 days of the first DTaP dose and 1 month after the third dose. BCG vaccine, given simultaneously with the DTaP vaccine, did not influence the immunogenicity of the acellular pertussis vaccine components when compared with separate administration of the two vaccines. Infants immunised according to a 2-4-6-month schedule had a significantly higher immune response than those immunised according to a 2-3-4-month schedule with respect to the response to pertussis toxoid assessed by seroneutralisation on Chinese hamster ovary cells (P<0.0001). These results suggest that BCG and DTaP vaccines can be given simultaneously without interference or enhancement and that more optimal immunogenicity is achieved with an extended than with an accelerated schedule. FAU - Simondon, F AU - Simondon F AD - Unite de Recherche sur les Maladies Infectieuses et Parasitaires, Institut Francais de Recherche Scientifique pour le Developpement en Cooperation (ORSTOM), Montpellier. Francois.Simondon@mpl.orstom.fr FAU - Preziosi, M P AU - Preziosi MP FAU - Pinchinat, S AU - Pinchinat S FAU - Yam, A AU - Yam A FAU - Chabirand, L AU - Chabirand L FAU - Wassilak, S AU - Wassilak S FAU - Pines, E AU - Pines E FAU - Trape, J F AU - Trape JF FAU - Salomon, H AU - Salomon H FAU - Hoffenbach, A AU - Hoffenbach A LA - eng PT - Clinical Trial PT - Journal Article PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - Germany TA - Eur J Clin Microbiol Infect Dis JT - European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology JID - 8804297 RN - 0 (Antibodies, Bacterial) RN - 0 (BCG Vaccine) RN - 0 (Diphtheria-Tetanus-Pertussis Vaccine) RN - 0 (Diphtheria-Tetanus-acellular Pertussis Vaccines) RN - 0 (Toxoids) RN - 0 (pertussis toxoid) SB - IM MH - Antibodies, Bacterial/*biosynthesis MH - BCG Vaccine/administration & dosage/*immunology MH - Bordetella pertussis/*immunology MH - Diphtheria-Tetanus-Pertussis Vaccine/administration & dosage/*immunology MH - Diphtheria-Tetanus-acellular Pertussis Vaccines MH - Humans MH - Immunization Schedule MH - Infant MH - Malaria/immunology MH - Senegal MH - Toxoids/immunology EDAT- 1999/04/07 00:00 MHDA- 1999/04/07 00:01 CRDT- 1999/04/07 00:00 PHST- 1999/04/07 00:00 [pubmed] PHST- 1999/04/07 00:01 [medline] PHST- 1999/04/07 00:00 [entrez] AID - 10.1007/s100960050221 [doi] PST - ppublish SO - Eur J Clin Microbiol Infect Dis. 1999 Jan;18(1):23-9. doi: 10.1007/s100960050221.