ReviewFrontiers in aging2026
Immune system ontogeny-a subtle evolution to perfection.
Review in Frontiers in aging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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5 authors.
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Abstract
It is well known that both innate and adaptive immune systems in newborns are immature, making them highly susceptible to infection. Additionally, pre-term newborns with hindered immune systems are more prone to increased mortality and morbidity. Newborns are capable of mounting adaptive immune responses, but their capability to develop long-lasting immunity is limited. Thus, the fetus and newborn's immune system is considered "immature" due to functional disorders in immune response or suppression by regulatory cells. Aging is another factor that leads to impaired immune responses due to a state of chronic low-grade inflammation (inflammaging), which compromises defense against pathogens and malignancies and favors the onset of age-related disorders. However, in this complicated scenario, centenarians emerged as a paradigm shift due to their particular immune system that prevents inflammaging and enables them to achieve longevity. Therefore, the present review aims to provide an updated overview of immune response development through neonatal, infant, and adult life in order to highlight stage-specific mechanisms and uniquely regulated immune responses. Taken together, this information provides mechanistic insights that can be harnessed to develop age-adapted interventional strategies and prevent the onset of age-associated disorders in older adults.
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