2016
DOI: 10.1186/s12979-016-0079-7
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Changes in blood lymphocyte numbers with age in vivo and their association with the levels of cytokines/cytokine receptors

Abstract: BackgroundAlterations in the number and composition of lymphocytes and their subsets in blood are considered a hallmark of immune system aging. However, it is unknown whether the rates of change of lymphocytes are stable or change with age, or whether the inter-individual variations of lymphocyte composition are stable over time or undergo different rates of change at different ages. Here, we report a longitudinal analysis of T- and B-cells and their subsets, and NK cells in the blood of 165 subjects aged from… Show more

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Cited by 88 publications
(87 citation statements)
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References 43 publications
(52 reference statements)
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“…We found significant and global alterations in the B-cell compartment that underline the immune system's effort to make up for lymphopenia with the increase in transitional B cells and plasmablasts, besides the cytokine storm and the functional and phenotypic alterations of the T-cell compartment that we have recently described in this group of patients [14]. Of note, memory B cells, that are supposed to remain stable or slightly increase from 20 to 80 years [15,16], in our patients were significantly lower than those of controls, who were younger. This further evidences how deep was the B-cell impairment that we have found.…”
Section: Discussionmentioning
confidence: 59%
See 1 more Smart Citation
“…We found significant and global alterations in the B-cell compartment that underline the immune system's effort to make up for lymphopenia with the increase in transitional B cells and plasmablasts, besides the cytokine storm and the functional and phenotypic alterations of the T-cell compartment that we have recently described in this group of patients [14]. Of note, memory B cells, that are supposed to remain stable or slightly increase from 20 to 80 years [15,16], in our patients were significantly lower than those of controls, who were younger. This further evidences how deep was the B-cell impairment that we have found.…”
Section: Discussionmentioning
confidence: 59%
“…Twenty milliliters of blood was collected in vacuette containing EDTA and immediately processed according to biosafety rules [25]. Isolation of PBMC was performed by using Ficoll-Paque according to standard procedures [15]. PBMC were stored in liquid nitrogen in FBS added with 10% DMSO until analysis.…”
Section: Blood Collection and Pbmc Isolationmentioning
confidence: 99%
“…Our statistical model suggests that older age contributes to decreased CD4 1 and CD8 1 T-lymphocyte counts; however, previous data suggest that aging is associated with smaller decreases in these cell counts than predicted by our model. [23][24][25][26][27] Even if there remains concern for bias related to an age imbalance among our groups, the finding of CD4 1 T-lymphocyte counts ,200 cells per microliter in a healthy population, regardless of age, is surprising. The homeostatic mechanisms that maintain a given peripheral blood T-cell count are incompletely understood but appear to depend on cytokines like interleukin-7 and interleukin-15, which were not measured in this study.…”
Section: Discussionmentioning
confidence: 78%
“…However, T‐cell memory developed earlier in life generally functions well into old age, formation of specific antibodies to novel infections and generation of novel immune responses is significantly impaired later in life (Haynes & Maue ). These changes are a result of reduced cell function and depletion of naïve cells due to accumulated exposure to antigens (‘life‐long antigenic load’) (Lin et al ). Given the generality of such mechanisms across taxa (Shanley et al ), we predicted a decline with age in adaptive immune function.…”
Section: Discussionmentioning
confidence: 99%