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Maternal immunization with Group B Streptococcus six-valent polysaccharide conjugate vaccine supported by lack of toxicity in rat and rabbit fertility and developmental toxicity studies.
Catlin, Natasha R; Cappon, Gregg D; Engel, Scott; Rohde, Cynthia; Nowland, William S; Buitrago, Sandra; Scully, Ingrid; Anderson, Annaliesa S; Bowman, Christopher J.
Afiliação
  • Catlin NR; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Groton, Connecticut, USA.
  • Cappon GD; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Groton, Connecticut, USA.
  • Engel S; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Groton, Connecticut, USA.
  • Rohde C; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Pearl River, New York, USA.
  • Nowland WS; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Groton, Connecticut, USA.
  • Buitrago S; Vaccine Research and Development, Pfizer Worldwide Research and Development, Pearl River, New York, USA.
  • Scully I; Vaccine Research and Development, Pfizer Worldwide Research and Development, Pearl River, New York, USA.
  • Anderson AS; Vaccine Research and Development, Pfizer Worldwide Research and Development, Pearl River, New York, USA.
  • Bowman CJ; Drug Safety Research and Development, Pfizer Worldwide Research and Development, Groton, Connecticut, USA.
Birth Defects Res ; 113(19): 1343-1356, 2021 11 15.
Article em En | MEDLINE | ID: mdl-34516044
A maternal Group B Streptococcus (GBS) six-valent polysaccharide conjugate vaccine (GBS6) is being developed to protect neonates and infants up to 3 months of age through passive transfer of antibodies from the mother to the infant. Fertility and developmental toxicity studies were conducted in female Sprague Dawley rats and New Zealand White rabbits with GBS6 (20 µg capsular polysaccharide/serotype formulated with or without AlPO4 , the highest clinical dose). Females were administered the full human dose of the GBS6 formulation intramuscularly twice prior to mating and twice during gestation, to ensure that high antibody levels were maintained throughout gestation and lactation. Approximately, half of the rats and rabbits were evaluated at the end of gestation, and the remainder were evaluated at the end of lactation. Maternal blood for GBS6 serology, to measure antibody titers to the GBS6 antigens, was collected prior to the first dose, prior to mating, and at each necropsy. Blood for serology was also collected from offspring at the end of gestation and lactation. In both species, there was no evidence of vaccine-related effects on fertility, embryo-fetal development, or postnatal development of the offspring, supporting regulatory guidance that single-species evaluation would have been sufficient. Functional serum antibodies to all six serotypes in the vaccine were confirmed in maternal animals and functional serum antibodies to one or more of the six serotypes was also confirmed in some rat offspring and most of the rabbit offspring. The results of these studies supported the safety of GBS6 vaccine administration to pregnant women.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_enfermedades_transmissibles Assunto principal: Streptococcus agalactiae / Imunização Tipo de estudo: Guideline Limite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 2_ODS3 Problema de saúde: 2_enfermedades_transmissibles Assunto principal: Streptococcus agalactiae / Imunização Tipo de estudo: Guideline Limite: Animals / Female / Humans / Pregnancy Idioma: En Revista: Birth Defects Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos
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