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- W4220762823 endingPage "104007" @default.
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- W4220762823 abstract "Neonatal immune-microbiota co-development is poorly understood, yet age-appropriate recognition of - and response to - pathogens and commensal microbiota is critical to health. In this longitudinal study of 148 preterm and 119 full-term infants from birth through one year of age, we found that postmenstrual age or weeks from conception is a central factor influencing T cell and mucosal microbiota development. Numerous features of the T cell and microbiota functional development remain unexplained; however, by either age metric and are instead shaped by discrete perinatal and postnatal events. Most strikingly, we establish that prenatal antibiotics or infection disrupt the normal T cell population developmental trajectory, influencing subsequent respiratory microbial colonization and predicting respiratory morbidity. In this way, early exposures predict the postnatal immune-microbiota axis trajectory, placing infants at later risk for respiratory morbidity in early childhood." @default.
- W4220762823 created "2022-04-03" @default.
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- W4220762823 date "2022-04-01" @default.
- W4220762823 modified "2023-10-01" @default.
- W4220762823 title "Aberrant newborn T cell and microbiota developmental trajectories predict respiratory compromise during infancy" @default.
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- W4220762823 doi "https://doi.org/10.1016/j.isci.2022.104007" @default.
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