Aged Chinese rhesus macaques suffer severe lymphocytic aging and can be served as a proper animal mo

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  Age is a major risk factor for morbidity and mortality for many infections caused by various pathogens.Many infectious diseases,such as influenza,tuberculosis and AIDS,often spread with greater frequency or severity in aged population.This way may be attributed to diminishing immune protection with age,which is commonly referred to as immunosenescence.Most studies over the past decades describing age-related modifications in immune system were based on rodent models.However,as a long-lived species of non-human primates and sharing greater genetic and physiological similarities with humans than rodent models,Rhesus macaques(RM,Macaca mulatta)can offer more distinct advantages to research immunosenescence.Here,we investigated phenotypic features of T and B-cell aging in peripheral blood from Chinese rhesus macaques(ChRM),included(1)a decrease of CD4/CD8 ratio;(2)a loss of na?ve T cells accompanied with elevated proliferation and expansion of effector memory subset;(3)a reduction in B cell numbers and a shift from na?ve B cells towards memory phenotype; and(4)increased levels of PD-1 expression in T cells and CD95 expression in B cells.Moreover,an accelerated decline in CD4+ T cells and na?ve T cells was found in male macaques,giving them a more severe immune risk profile.These data indicated Chinese rhesus macaques share a significant homology with humans in phenotypic aging of adaptive immunity,and may be an appropriate animal model for human aging research.
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