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- W136353521 endingPage "169" @default.
- W136353521 startingPage "119" @default.
- W136353521 abstract "Neonates, infants, and young children are at higher risk of infection and are more susceptible to serious consequences of infections than adults.This susceptibility results from limitations of both innate and adaptive (antigenspecific) immunity. All major lineages of hematopoietic cells that are part of the immune system are present in the human by the beginning of the second trimester, but their state of differentiation and their functional capacity may limit the immune response. In this chapter, we review general information about phenotypic and functional studies of antigen-presenting cells (APCs), T cells and B cells in the human neonate, infant, and young child, including responses to specific infectious agents and vaccines. To illustrate recent insights into the acquisition of antigen-specific immunity in the context of the developing immune system after the neonatal period, we summarize our recent investigations of immune responses in infants and young children with post-natally acquired human cytomegalovirus (CMV) infection and infants given live attenuated measles vaccine at six, nine or twelve months of age." @default.
- W136353521 created "2016-06-24" @default.
- W136353521 creator A5031397502 @default.
- W136353521 creator A5038633732 @default.
- W136353521 date "2005-01-01" @default.
- W136353521 modified "2023-09-26" @default.
- W136353521 title "Vaccination in the context of immunological immaturity" @default.
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