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The half-life of maternal transplacental antibodies against diphtheria, tetanus, and pertussis in infants: an individual participant data meta-analysis.
Oguti, Blanché; Ali, Asad; Andrews, Nick; Barug, Daan; Anh Dang, Duc; Halperin, Scott A; Thu Hoang, Ha Thi; Holder, Beth; Kampmann, Beate; Kazi, Abdul M; Langley, Joanne M; Leuridan, Elke; Madavan, Naomi; Maertens, Kirsten; Maldonado, Herberth; Miller, Elizabeth; Munoz-Rivas, Flor M; Omer, Saad B; Pollard, Andrew J; Rice, Thomas F; Rots, Nynke; Sundaram, Maria E; Wanlapakorn, Nasamon; Voysey, Merryn.
Afiliação
  • Oguti B; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, United Kingdom.
  • Ali A; Aga Khan University, Karachi, Pakistan.
  • Andrews N; Public Health England, United Kingdom.
  • Barug D; Centre for Infectious Disease Control, National Institute for Public Health and the Environment, the Netherlands.
  • Anh Dang D; National Institute of Hygiene and Epidemiology, Vietnam.
  • Halperin SA; Canadian Center for Vaccinology, Dalhousie University, Canada.
  • Thu Hoang HT; National Institute of Hygiene and Epidemiology, Vietnam.
  • Holder B; Department of Metabolism, Digestion and Reproduction, Imperial College London, United Kingdom.
  • Kampmann B; London School of Hygiene and Tropical Medicine, United Kingdom.
  • Kazi AM; Aga Khan University, Karachi, Pakistan.
  • Langley JM; Canadian Center for Vaccinology, Dalhousie University, Canada.
  • Leuridan E; Centre for the Evaluation of Vaccination, Vaccine & Infectious Diseases Institute, University of Antwerp, Belgium.
  • Madavan N; University of Exeter, United Kingdom.
  • Maertens K; Centre for the Evaluation of Vaccination, Vaccine & Infectious Diseases Institute, University of Antwerp, Belgium.
  • Maldonado H; Universidad del Valle de Guatemala, Guatemala.
  • Miller E; Public Health England, United Kingdom.
  • Munoz-Rivas FM; Baylor College of Medicine, USA.
  • Omer SB; Yale Institute for Global Health, USA.
  • Pollard AJ; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, United Kingdom.
  • Rice TF; Department of Metabolism, Digestion and Reproduction, Imperial College London, United Kingdom.
  • Rots N; Centre for Infectious Disease Control, National Institute for Public Health and the Environment, the Netherlands.
  • Sundaram ME; Center for Clinical Epidemiology and Population Health, Marshfield Clinic Research Institute, Marshfield, USA.
  • Wanlapakorn N; Center of Excellence in Clinical Virology, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Thailand.
  • Voysey M; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, United Kingdom. Electronic address: merryn.voysey@paediatrics.ox.ac.uk.
Vaccine ; 40(3): 450-458, 2022 01 24.
Article em En | MEDLINE | ID: mdl-34949496
AIM: There are few reliable estimates of the half-lives of maternal antibodies to the antigens found in the primary series vaccines. We aimed to calculate the half-lives of passively acquired diphtheria, tetanus and pertussis (DTP) antibodies in infants. We aimed to determine whether decay rates varied according to country, maternal age, gestational age, birthweight, World Bank income classifications, or vaccine received by the mother during pregnancy. METHODS: De-identified data from infants born to women taking part in 10 studies, in 9 countries (UK, Belgium, Thailand, Vietnam, Canada, Pakistan, USA, Guatemala and the Netherlands) were combined in an individual participant data meta-analysis. Blood samples were taken at two timepoints before any DTP-containing vaccines were received by the infant: at birth and at 2-months of age. Decay rates for each antigen were log2-transformed and a mixed effects model was applied. Half-lives were calculated by taking the reciprocal of the absolute value of the mean decay rates. RESULTS: Data from 1426 mother-infant pairs were included in the analysis. The half-lives of the 6 antigen-specific maternal antibodies of interest were similar, with point estimates ranging from 28.7 (95% CI: 24.4 - 35) days for tetanus toxoid antibodies to 35.1 (95% CI: 30.7 - 41.1) days for pertactin antibodies. The decay of maternal antibodies did not significantly differ by maternal age, gestational age, birthweight, maternal vaccination status or type of vaccine administered. CONCLUSION: Maternal antibodies decay at different rates for the different antigens; however, the magnitude of the difference is small. Decay rates are not modified by key demographic or vaccine characteristics.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Tétano / Coqueluche / Difteria Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Vaccine Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Tétano / Coqueluche / Difteria Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Female / Humans / Infant / Newborn / Pregnancy Idioma: En Revista: Vaccine Ano de publicação: 2022 Tipo de documento: Article