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Modestly protective cytomegalovirus vaccination of young children effectively prevents congenital infection at the population level.
Byrne, Catherine; Coombs, Daniel; Gantt, Soren.
Afiliação
  • Byrne C; Department of Microbiology and Immunology, The University of British Columbia, 1365-2350 Health Sciences Mall, Vancouver, British Columbia V6T 1Z3, Canada; British Columbia Children's Hospital Research Institute, 938 W 28th Ave, Vancouver, British Columbia V5Z 4H4, Canada; Institute of Applied Mathematics, The University of British Columbia, 311-6356 Agricultural Road, Vancouver, British Columbia V6T 1Z2, Canada. Electronic address: cbyrne@bcchr.ubc.ca.
  • Coombs D; Institute of Applied Mathematics, The University of British Columbia, 311-6356 Agricultural Road, Vancouver, British Columbia V6T 1Z2, Canada; Department of Mathematics, The University of British Columbia, 1984 Mathematics Road, Vancouver, British Columbia V6T 1Z2, Canada. Electronic address: coombs@math.ubc.ca.
  • Gantt S; Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, 2900, boul. Édouard-Montpetit, Montreal, Québec H3T 1J4, Canada; Centre de Recherche du CHU Sainte-Justine, 3175 chemin de la Côte-Sainte-Catherine, Montréal, Québec H3T 1C5, Canada. Electronic address: soren.gantt@umontreal.ca.
Vaccine ; 40(35): 5179-5188, 2022 08 19.
Article em En | MEDLINE | ID: mdl-35907677
ABSTRACT
A vaccine to prevent congenital cytomegalovirus infection (cCMV) is a public health priority. cCMV results from maternal primary or non-primary CMV infection (reinfection, or reactivation of chronic infection) during pregnancy. Young children are a major source of transmission to pregnant women because they shed CMV at high viral loads for prolonged periods. CMV vaccines evaluated in clinical trials so far have demonstrated only approximately 50% efficacy against maternal primary infection. None of these have been approved, as higher levels of vaccine efficacy are assumed to be required to substantially reduce cCMV prevalence. Here, we designed a mathematical model to capture the relationship between viral shedding by young children and maternal CMV infections during pregnancy. Using this model, we were able to quantify the impact of CMV post-infection immunity on protecting against reinfection and viral shedding. There was a 36% reduction in the risk of infection to a seropositive person with post-infection immunity (reinfection) versus a seronegative person without this immunity (primary infection), given the same exposure. Viral shedding following reinfection was only 34% the quantity of that following primary infection. Our model also predicted that a vaccine that confers the equivalent of post-infection immunity, when given to young children, would markedly reduce both CMV transmission to pregnant women and the prevalence of cCMV. Thus, we predict that existing vaccine candidates that have been shown to be only modestly protective may in fact be highly effective at preventing cCMV by interrupting child-to-mother transmission.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Doenças Transmissíveis / Infecções por Citomegalovirus / Vacinas contra Citomegalovirus / Doenças Fetais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Complicações Infecciosas na Gravidez / Doenças Transmissíveis / Infecções por Citomegalovirus / Vacinas contra Citomegalovirus / Doenças Fetais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child, preschool / Female / Humans / Pregnancy Idioma: En Ano de publicação: 2022 Tipo de documento: Article