Changes in blood lymphocyte numbers with age in vivo and their association with the levels of cytokines/cytokine receptors
- Yun Lin†1,
- Jiewan Kim†1,
- E. Jeffrey Metter2, 3,
- Huy Nguyen1,
- Thai Truong1,
- Ana Lustig1,
- Luigi Ferrucci2 and
- Nan-ping Weng1Email author
© The Author(s). 2016
Received: 4 March 2016
Published: 18 August 2016
Alterations 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 24 to 90 years, with each subject assessed at baseline and an average of 5.6 years follow-up.
The rates of change of T-(CD4+ and CD8+) and B-cells, and NK cells were relative stable throughout the adult life. A great degree of individual variations in numbers of lymphocytes and their subsets and in the rates of their changes with age was observed. Among them, CD4+ T cells exhibited the highest degree of individual variation followed by NK cells, CD8+ T cells, and B cells. Different types of lymphocytes had distinct trends in their rates of change which did not appear to be influenced by CMV infection. Finally, the rates of CD4+, CD8+ T cells, naive CD4+ and naïve CD8+ T cells were closely positively correlated.
Our findings provide evidence that the age-associated changes in circulating lymphocytes were at relative stable rates in vivo in a highly individualized manner and the levels of selected cytokines/cytokine receptors in serum might influence these age-associated changes of lymphocytes in circulation.
KeywordsAging Human Peripheral blood Lymphocytes CD4 and CD8 T cell B cell NK cell CMV
Decline in immune function with age is viewed as a fundamental problem for the increased risk of age-associated diseases or disabilities [1–3]. One of the hallmark changes in the immune system with age is the alteration of the number and composition of different types of lymphocytes in the circulation. In older individuals, the numbers of CD4 + and CD8 + T cells and B cells are reduced whereas the numbers of NK cells are increased as compared to younger individuals [4, 5]. At the subset level, decreases of naïve T and B cells and increases of memory T and B cells also occurs with aging [6–11]. Such changes may reflect a combination of reduced production of naïve lymphocytes and the accumulation of memory lymphocytes as the results of the reduced overall production of lymphocytes and of the host-environment interaction over time. Despite the overall trend of age-associated changes, striking variations in the numbers of lymphocytes exist between individuals. It is currently unknown whether the observed variations are due to stable characteristics that are maintained over time or whether different subjects have different rates of change with aging.
In the T cell compartment, age associated reduction of CD4 + and CD8 + T cells as a percentage of peripheral blood mononuclear cells (PBMCs) as well as absolute numbers (cell/μl) in blood have been reported [5, 12, 13]. Within the T cell subsets, in addition to reduced naïve and increased memory CD4 + and CD8 + T cells with age, studies have shown that CD4 + regulatory T cells and CD8 + CD28- T cells increase with age [14–16]. Thymic involution is the single most critical contributor of reduction in naïve T cells with age  whereas cumulative encounters with antigens over time is the force driving the increase memory T cells , CD8 + CD28- T cells , as well as Tregs . A similar decrease of naïve and increase of memory B cells also occurs in the B cell compartment but the magnitude of change is not as profound as what is observed in T cells [6, 20]. Interestingly, natural killer cells (NK cells) are the only lymphoid linage cells that increase with aging [4, 21, 22]. However, the cytotoxic activity of NK cells appears to be reduced with age and thus the increase in NK cell number may be interpreted as compensatory. Some of the alterations in lymphocyte composition are considered biomarkers of immunosenenscence (ratio of CD4/CD8, increase of CD28- T cells, and increase of NK cells) because they are associated with mortality in elderly [23, 24].
Information regarding age-related changes in lymphocyte composition in humans is mostly derived from cross-sectional studies. This approach may be biased by selective mortality or participation attrition and, in addition, lack the time dimension necessary to dissect cross-sectional and longitudinal effects. Data from longitudinal studies should allow for the determination of whether changes in lymphocyte compositions occur at a constant rate or are non-linear over time and whether there are detectable causes of these changes.
Here, we conducted a longitudinal analysis of CD4 + and CD8 + T cells, B cells and their subsets, and NK cells in 165 participants from the Baltimore Longitudinal Study of Aging (BLSA) (https://www.blsa.nih.gov/) assessed at baseline and, on average, after a 5-year follow-up. We analyzed the rates of changes and explored potential causes of variations and correlation among these changes and with CMV infection. Our findings provide detailed longitudinal rates of changes in lymphocytes and their subsets with aging in a relatively healthy population dispersed over a relatively wide age-range.
Study design and participants
We performed a longitudinal study of T- and B-cells and their subsets, and NK cells in peripheral blood of 165 BLSA participants at first visit and 5-year follow-up under the NIH IRB- approved protocol (GRC98-12-28-01) and performed in accordance with the Declaration of Helsinki. Demographic characterization of these participants was summarized in Additional file 1: Table S1. At each visit, blood cell counts were measured by standard complete blood cell counts by Coulter Counter and PBMCs were isolated from 50 mL blood drawn from participants under fasting condition and cryopreserved in liquid nitrogen. Two to five cryopreserved PBMCs from each subject with an average of 5.6 years apart were used in the experiments. PBMCs from all time points were thawed and counted on the day of the experiment. The recovery of frozen PBMC was 77 % ± 0.3 % (mean ± SEM). Complete blood cell counts was combined with flow cytometry analysis (see gating strategy in Additional file 1: Figure S1) to obtain the cell count and to estimate rate changes for different cell populations.
Analysis by flow cytometry
Antibodies used for flow cytometry analysis included: CD2-Tri-Color (TC); CD4-Phycoerythrin (PE) and CD4Allophycocyanin (APC); CD28-Fluorescein Isothiocyanate (FITC); CD8-TC; CD19-APC; CD45RA-APC; CD16-FITC from Life Technologies (Grand Island, NY); CD14-PE; CD27-PE; and IgM-FITC from BD Biosciences (San Jose, CA). Freshly thawed PBMCs from each visit were stained with three to five antibodies: T cells (CD2, CD4, CD8, CD45RA, and CD28); B cells (CD19, IgM, and CD27); NK cells (CD16). The data were collected on a BD FACSCalibur or BD FACSCanto II, and analyzed by Cell-Quest (BD Biosciences) and FlowJo. The gating strategies were presented in Additional file 1: Figure S1.
Measurement of selected biomarkers and CMV IgG
Fasting blood was collected at each visit for measurement of complete blood cell count and other routine blood chemistry using the standard method under the BLSA protocol. Sera were isolated from blood and stored in a -80 °C freezer prior to cytokine (IL) measurement using a custom-made multiplex assay (BioRad Luminex Assays) according to the manufacturer’s instruction. CMV IgG was measured from sera of 120 subjects (117 of them had two time points and 3 had single time points) using the ELISA kit (Abcam, # ab108639) according to the manufacturer’s instruction.
Figures were plotted as scatterplots with a linear regression line. The regression lines for rate and percentage rate of change by age were analyzed using linear regression. Regressions of number of cells and percent of cells were tested using mixed effects linear regression on age with a random effect for subject to address the within-subject correlation with the repeated measurements. The inclusion of the time difference between the measurements did not affect the assessment. For the regression models, all tests were performed with a p < 0.05. Correlations were calculated between pairs of variables, and after adjusting by FDR , p value less or equal to 0.005 is considered as significant. To address the question whether rapid rates of change are present across more cell types than expected, rates for each cell type were dichotomized and summed to identify subjects in the tertile with the greatest rate of cell loss (except for NK rates which were the highest tertile). The summed score was compared to the expected binomial distribution by chi-squared test. Assuming a binomial distribution, the probability coefficient was estimated from the data using the Bayesian modeling program rstan (http://mc-stan.org/rstan.html). A single sample proportion test was used to test whether the proportion of subject with summed score of 4 or more was greater in the data as compared to the expected summed score of 4 or more from a binomial distribution with probability of 0.33.
All statistical analyses were done using R version 2.12.1 (http://www.r-project.org).
Changes of CD4+ T cells and their subsets in peripheral blood with age in vivo
Changes in CD8+ T cells and their subsets in peripheral blood with age in vivo
Changes in B cells and their subsets in peripheral blood with age in vivo
Change of NK cell and its subsets in peripheral blood with age in vivo
Correlation between changes among different types of lymphocytes and selected cytokines and soluble cytokine receptors, and antibodies against cytomegalovirus (CMV) in blood
The rate of naïve CD4+ T cells was positively correlated with the rates of change of CD4+, CD8+ and naïve CD8+ T cells but negatively correlated with numbers of CD4+ and naïve CD4+, and naïve CD8+ T cells (Fig. 5). The rate of Treg cells was positively correlated with numbers of CD4+ and naïve CD4+ T cells, and rate of CD4+CD28- cells (Fig. 5). To determine whether there is a tendency for subjects who show rapid rates of change in one cell type to show similar changes in other cell types, we dichotomized the rates for each cell type to identify subjects in the tertile with the greatest rate of cell loss (except for NK rates which were the highest tertile) and the seven dichotomized rates were summed (total score 0 to 7). If the cell rates are independent, the distribution should be binomial with probability 0.33, which was not the case by chi-squared test (p < 0.0001). The probability which fits the summed score was 0.38 that is significantly different that the 0.33 used in creating the score (p < 0.02). If the cell rates occur together, the expectation would be for an excessive proportion of subjects to have high summed scores. The expected probability of a score of 4 or more is 0.17, while the observed proportion is 0.23 (p = 0.03). The high proportion of high counts argues that there is evidence that rapid rates tend to co-occur among cell types far more often than would be expected by chance (i.e. being independent). Finally, the rate of CD4+CD28- cells was positively correlated with the rates of CD4+, Treg and CD8+CD28- T cells (Fig. 5).
The rate of CD8+ T cells showed a positive correlation with the rates of CD8+CD28-, naïve CD8+, total CD4+, naïve CD4+ T cells and serum level of IL-15 and a negative correlation with number of CD8+ T cells, CD8+CD28- T cells, and rate of naïve B cells (Fig. 5). The rate of change of naïve CD8+ T cells was positively correlated with rates of change of CD4+, CD8+, and naïve CD4+ T cells but negatively correlated with the numbers of naïve CD8+ T cells (Fig. 5). Finally, the rate of change of CD8+CD28- T cells was positively correlated with the rates of CD8+, CD4+, CD4+CD28- and serum level of IL-15 but negatively corrected with numbers of CD8+ CD8+CD28- T cells, and rate of naïve B cells (Fig. 5). The ratio of CD4+/CD8+ T cell number was positively correlated with numbers of CD4+, Treg, and naïve CD4+ but negatively numbers of CD8+, CD8+CD28-, and naïve CD8 T cells, and CMV seropositivity defined by the presence of anti-CMV IgG antibodies in sera (Fig. 5). The association CMV seropositivity with the low ratio of CD4+/CD8+ found here is in agreement with the previous report .
The rate of B cells was positively correlated with serum levels of soluble TNFRI and TNFRII, and rates of naïve and memory B cells but was negatively correlated with the numbers of B cells and naïve B cells (Fig. 5). The rate of naïve B cells was positively correlated with rate of B cells but negatively correlated with numbers of naïve B, naïve B cells, rates of CD8+CD28- and CD8+ T cells (Fig. 5). The rate of change of memory B cells was positively correlated with serum levels of soluble TNFRI and numbers of NK cells (Fig. 5). Finally, the rate of change of NK cells was negatively correlated with the serum level of triglyceride (Fig. 5).
Limited information is available regarding the trajectories of in vivo aging of immune cells in humans. As lymphocyte numbers in peripheral blood exhibit a great degree of individual variation, it is unclear whether inter-individuals differences are due to individual’s characteristics that remain stable with aging or result from the different rates of changes in different types of lymphocytes in across individuals. Our longitudinal analysis showed that the rates of changes of all four major types of lymphocytes (CD4+, CD8+, B, and NK cells) were also highly individualized. The average rates of change of all four major types of lymphocytes were quite stable in the study subjects across 70 years of adult life. It will be necessary to further examine these changes in a longer time follow-up such as 10 or 20 years to understand the contributing genetic and environmental factors that determine the individual variation. Such a study will require long-term commitment and resources but the yield will have the details and resolution needed to better understand these age-associated changes within the immune system.
One of the most prominent signs of an immune system aging is a significant reduction of naïve lymphocytes in blood. The reduction of naïve lymphocytes occurs continuously with advancing age, which has been mainly attributed to a reduction of thymic output after puberty and imperfect peripheral maintenance. However, it is unknown whether the loss of naïve lymphocytes occurs at a constant or increasing rate with age. Our longitudinal analysis showed that the trends of rates of change of naïve CD4 + and CD8 + T cell and naïve B cells over 70 years of adult life were remarkably flat, indicating that the continuous reduction of naïve T and B cells in blood is due to a cumulative effect during aging. This conclusion is further supported by study using 2H2O labeling showed similar dynamics of lymphocytes between young and elderly subjects . In contrast to naïve lymphocytes, CD28- T cells (both CD4+ and CD8+) and NK cells increase in blood with age. Interestingly, we observed that the trends of the rates of change of CD4+CD28- T cells and NK cells (Figs. 1c and 4a) but not CD8+CD28- T cells (Fig. 2c) also slightly increase with age. This suggests that age-associated increase of CD4+CD28- T cells and NK cells with age is not only accumulated over time but also increased in pace with age.
A reduced CD4 + /CD8 + ratio is considered as one of the immune risk phenotypes (IRP) related to increased morbidity and mortality in elderly [23, 24, 34, 35]. In agreement with previous finding , we also found that the ratio of CD4/CD8 T cells is negatively correlated with CMV seropositivity and the trend of the CD4 + /CD8 + ratio was not substantially changed with age (Fig. 2e). Collectively, these findings suggest that a reduction in the CD4 + /CD8 + ratio is not a general change with age in this study cohort but is more obvious to the CMV infected old subjects.
Correlational analysis of the rates of change of lymphocytes and their subsets with some selected cytokines and soluble cytokine receptors revealed some unexpected findings. We found that the rates of CD8+ and CD8+ CD28-T cells were positively correlated with levels of serum IL-15. In contrast to T cells, rates of B cells and memory B cells were positively correlated with soluble TNF-RI. IL-15 is a critical growth factor for CD8+ T cells  and TNF alpha can induce B cell proliferation , their positive correlations suggest that cytokine mediated peripheral expansion is an influencing factor of the rate of changes.
We have applied 11 cell lineage/differentiation makers in analyzing 4 major lymphocyte populations in blood. Although using frozen PBMCs in this study prevents selection of those temperature sensitive markers such as CD62L and CCR7, there are more differentiation markers that can be used to improve the resolution and precision of age-associated changes in these lymphocyte subsets. In particular, applying IgD and IgG staining could further separate naïve and memory B cell subpopulations as some of those subpopulations display more obvious age-related changes [41–43]. Therefore, further study is warranted to precisely assess the age-associated change of lymphocyte composition and function in vivo.
In conclusion, our findings showed that the rates of changes in T (CD4 + and CD8 + ), B, NK cells and their subsets are highly individualized, exhibiting a wide range regardless of the subject’s age and the average trends of the rates of changes were relatively flat over 70 years of adult life. Unexpectedly, we observed significant associations of the serum levels of certain cytokines and cytokine receptors with the rates of change in selected lymphocytes and their subjects. Collectively, our findings provide much needed information of the in vivo changes of lymphocyte compositions and numbers in blood with age, the interrelationship among different type of lymphocytes and their subsets, and potential contributions of serum cytokines/cytokine receptors in these age-associated changes. Future study with a longer time span, samples with multiple time points and assessment with more differentiation markers will further enhance our understanding of how and when the alterations of lymphocyte type, composition, and number occur, and will be essential to better guide clinical interventions such as vaccination with improved precision and efficacy in the elderly.
We thank the NIA clinical core lab for collecting blood samples; all BLSA participants in this study, and Annette Ko for making the cluster graph.
This research work was supported entirely by the Intramural Research Program of the National Institute on Aging, National Institutes of Health (NIH).
Availability of data and material
The data used in this study will be available upon request.
YL, JK, HY, TT, and AL contributed to this manuscript in designing, conducting experiments, and data analysis. JM performed statistical analysis of the data. NPW and LF supervised the project. NPW and JK wrote the manuscript with approval from all authors. All authors discussed and reviewed the results of the project.
The authors declare that they have no competing interests.
Ethics approval and consent to participate
This study project is reviewed and approved by NIH IRB under the protocol (GRC98-12-28-01) and performed in accordance with the Declaration of Helsinki. All BLSA participants were consented which were used in this study.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Frasca D, Riley RL, Blomberg BB. Humoral immune response and B-cell functions including immunoglobulin class switch are downregulated in aged mice and humans. Semin Immunol. 2005;17:378–84.View ArticlePubMedGoogle Scholar
- Goronzy JJ, Weyand CM. Understanding immunosenescence to improve responses to vaccines. Nat Immunol. 2013;14:428–36.View ArticlePubMedPubMed CentralGoogle Scholar
- Weng NP. Aging of the immune system: how much can the adaptive immune system adapt? Immunity. 2006;24:495–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Le Garff-Tavernier M, Beziat V, Decocq J, Siguret V, Gandjbakhch F, Pautas E, et al. Human NK cells display major phenotypic and functional changes over the life span. Aging Cell. 2010;9:527–35.View ArticlePubMedGoogle Scholar
- Sansoni P, Cossarizza A, Brianti V, Fagnoni F, Snelli G, Monti D, et al. Lymphocyte subsets and natural killer cell activity in healthy old people and centenarians. Blood. 1993;82:2767–73.PubMedGoogle Scholar
- Chong Y, Ikematsu H, Yamaji K, Nishimura M, Nabeshima S, Kashiwagi S, et al. CD27+ (memory) B cell decrease and apoptosis-resistant CD27− (naive) B cell increase in aged humans: implications for age-related peripheral B cell developmental disturbances. Int Immunol. 2005;17:383–90.View ArticlePubMedGoogle Scholar
- Colonna-Romano G, Bulati M, Aquino A, Scialabba G, Candore G, Lio D, et al. B cells in the aged: CD27, CD5, and CD40 expression. Mech Ageing Dev. 2003;124:389–93.View ArticlePubMedGoogle Scholar
- Fagnoni FF, Vescovini R, Passeri G, Bologna G, Pedrazzoni M, Lavagetto G, et al. Shortage of circulating naive CD8+ T cells provides new insights on immunodeficiency in aging. Blood. 2000;95:2860–8.PubMedGoogle Scholar
- Kang I, Hong MS, Nolasco H, Park SH, Dan JM, Choi JY, et al. Age-associated change in the frequency of memory CD4+ T cells impairs long term CD4+ T cell responses to influenza vaccine. J Immunol. 2004;173:673–81.View ArticlePubMedGoogle Scholar
- Kilpatrick RD, Rickabaugh T, Hultin LE, Hultin P, Hausner MA, Detels R, et al. Homeostasis of the Naive CD4+ T cell compartment during aging. J Immunol. 2008;180:1499–507.View ArticlePubMedPubMed CentralGoogle Scholar
- Stervbo U, Bozzetti C, Baron U, Jurchott K, Meier S, Malzer JN, et al. Effects of aging on human leukocytes (part II): immunophenotyping of adaptive immune B and T cell subsets. Age (Dordr). 2015;37:93.View ArticleGoogle Scholar
- Lin Y, Damjanovic A, Metter EJ, Nguyen H, Truong T, Najarro K, et al. Age-associated telomere attrition of lymphocytes in vivo is co-ordinated with changes in telomerase activity, composition of lymphocyte subsets and health conditions. Clin Sci (Lond). 2015;128:367–77.View ArticleGoogle Scholar
- Simone R, Zicca A, Saverino D. The frequency of regulatory CD3+CD8+. J Leukoc Biol. 2008;84:1454–61.View ArticlePubMedGoogle Scholar
- Trzonkowski P, Szmit E, Mysliwska J, Mysliwski A. CD4+CD25+ T regulatory cells inhibit cytotoxic activity of CTL and NK cells in humans-impact of immunosenescence. Clin Immunol. 2006;119:307–16.View ArticlePubMedGoogle Scholar
- Czesnikiewicz-Guzik M, Lee WW, Cui D, Hiruma Y, Lamar DL, Yang ZZ, et al. T cell subset-specific susceptibility to aging. Clin Immunol. 2008;127:107–18.View ArticlePubMedPubMed CentralGoogle Scholar
- Weng NP, Akbar AN, Goronzy J. CD28(−) T cells: their role in the age-associated decline of immune function. Trends Immunol. 2009;30:306–12.View ArticlePubMedPubMed CentralGoogle Scholar
- Palmer DB. The effect of age on thymic function. Front Immunol. 2013;4:316.View ArticlePubMedPubMed CentralGoogle Scholar
- Nikolich-Zugich J. Aging of the T cell compartment in mice and humans: from no naive expectations to foggy memories. J Immunol. 2014;193:2622–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Jagger A, Shimojima Y, Goronzy JJ, Weyand CM. Regulatory T cells and the immune aging process: a mini-review. Gerontology. 2014;60:130–7.View ArticlePubMedGoogle Scholar
- Morbach H, Eichhorn EM, Liese JG, Girschick HJ. Reference values for B cell subpopulations from infancy to adulthood. Clin Exp Immunol. 2010;162:271–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Chidrawar SM, Khan N, Chan YL, Nayak L, Moss PA. Ageing is associated with a decline in peripheral blood CD56bright NK cells. Immun Ageing. 2006;3:10.View ArticlePubMedPubMed CentralGoogle Scholar
- Gayoso I, Sanchez-Correa B, Campos C, Alonso C, Pera A, Casado JG, et al. Immunosenescence of human natural killer cells. J Innate Immun. 2011;3:337–43.View ArticlePubMedGoogle Scholar
- Huppert FA, Pinto EM, Morgan K, Brayne C. Survival in a population sample is predicted by proportions of lymphocyte subsets. Mech Ageing Dev. 2003;124:449–51.View ArticlePubMedGoogle Scholar
- Wikby A, Ferguson F, Forsey R, Thompson J, Strindhall J, Lofgren S, et al. An immune risk phenotype, cognitive impairment, and survival in very late life: impact of allostatic load in Swedish octogenarian and nonagenarian humans. J Gerontol A Biol Sci Med Sci. 2005;60:556–65.View ArticlePubMedGoogle Scholar
- Benjamini Y, Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. J R Stat Soc Ser B. 1995;57:289–300.Google Scholar
- Fahey JL, Schnelle JF, Boscardin J, Thomas JK, Gorre ME, Aziz N, et al. Distinct categories of immunologic changes in frail elderly. Mech Ageing Dev. 2000;115:1–20.View ArticlePubMedGoogle Scholar
- Utsuyama M, Hirokawa K, Kurashima C, Fukayama M, Inamatsu T, Suzuki K, et al. Differential age-change in the numbers of CD4+CD45RA+ and CD4+CD29+ T cell subsets in human peripheral blood. Mech Ageing Dev. 1992;63:57–68.View ArticlePubMedGoogle Scholar
- den Braber I, Mugwagwa T, Vrisekoop N, Westera L, Mogling R, de Boer AB, et al. Maintenance of peripheral naive T cells is sustained by thymus output in mice but not humans. Immunity. 2012;36:288–97.View ArticleGoogle Scholar
- Wertheimer AM, Bennett MS, Park B, Uhrlaub JL, Martinez C, Pulko V, et al. Aging and cytomegalovirus infection differentially and jointly affect distinct circulating T cell subsets in humans. J Immunol. 2014;192:2143–55.View ArticlePubMedPubMed CentralGoogle Scholar
- Gregg R, Smith CM, Clark FJ, Dunnion D, Khan N, Chakraverty R, et al. The number of human peripheral blood CD4+ CD25high regulatory T cells increases with age. Clin Exp Immunol. 2005;140:540–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Cossarizza A, Ortolani C, Paganelli R, Barbieri D, Monti D, Sansoni P, et al. CD45 isoforms expression on CD4+ and CD8+ T cells throughout life, from newborns to centenarians: implications for T cell memory. Mech Ageing Dev. 1996;86:173–95.View ArticlePubMedGoogle Scholar
- Rea IM, Stewart M, Campbell P, Alexander HD, Crockard AD, Morris TC. Changes in lymphocyte subsets, interleukin 2, and soluble interleukin 2 receptor in old and very old age. Gerontology. 1996;42:69–78.View ArticlePubMedGoogle Scholar
- Provinciali M, Moresi R, Donnini A, Lisa RM. Reference values for CD4+ and CD8+ T lymphocytes with naive or memory phenotype and their association with mortality in the elderly. Gerontology. 2009;55:314–21.View ArticlePubMedGoogle Scholar
- Ferguson FG, Wikby A, Maxson P, Olsson J, Johansson B. Immune parameters in a longitudinal study of a very old population of Swedish people: a comparison between survivors and nonsurvivors. J Gerontol A Biol Sci Med Sci. 1995;50:B378–82.View ArticlePubMedGoogle Scholar
- Pawelec G, Ouyang Q, Colonna-Romano G, Candore G, Lio D, Caruso C. Is human immunosenescence clinically relevant? Looking for ‘immunological risk phenotypes’. Trends Immunol. 2002;23:330–2.View ArticlePubMedGoogle Scholar
- Borrego F, Alonso MC, Galiani MD, Carracedo J, Ramirez R, Ostos B, et al. NK phenotypic markers and IL2 response in NK cells from elderly people. Exp Gerontol. 1999;34:253–65.View ArticlePubMedGoogle Scholar
- Wikby A, Johansson B, Olsson J, Lofgren S, Nilsson BO, Ferguson F. Expansions of peripheral blood CD8 T-lymphocyte subpopulations and an association with cytomegalovirus seropositivity in the elderly: the Swedish NONA immune study. Exp Gerontol. 2002;37:445–53.View ArticlePubMedGoogle Scholar
- Westera L, van Hoeven V, Drylewicz J, Spierenburg G, van Velzen JF, De Boer RJ, et al. Lymphocyte maintenance during healthy aging requires no substantial alterations in cellular turnover. Aging Cell. 2015;14:219–27.View ArticlePubMedPubMed CentralGoogle Scholar
- Weng NP, Liu K, Catalfamo M, Li Y, Henkart PA. IL-15 is a growth factor and an activator of CD8 memory T cells. Ann N Y Acad Sci. 2002;975:46–56.View ArticlePubMedGoogle Scholar
- Patke CL, Shearer WT. gp120- and TNF-alpha-induced modulation of human B cell function: proliferation, cyclic AMP generation, Ig production, and B-cell receptor expression. J Allergy Clin Immunol. 2000;105:975–82.View ArticlePubMedGoogle Scholar
- Buffa S, Bulati M, Pellicano M, Dunn-Walters DK, Wu YC, Candore G, et al. B cell immunosenescence: different features of naive and memory B cells in elderly. Biogerontology. 2011;12:473–83.View ArticlePubMedGoogle Scholar
- Colonna-Romano G, Bulati M, Aquino A, Pellicano M, Vitello S, Lio D, et al. A double-negative (IgD−CD27−) B cell population is increased in the peripheral blood of elderly people. Mech Ageing Dev. 2009;130:681–90.View ArticlePubMedGoogle Scholar
- Kaminski DA, Wei C, Qian Y, Rosenberg AF, Sanz I. Advances in human B cell phenotypic profiling. Front Immunol. 2012;3:302.View ArticlePubMedPubMed CentralGoogle Scholar