- Open Access
Differential effects of age, cytomegalovirus-seropositivity and end-stage renal disease (ESRD) on circulating T lymphocyte subsets
Immunity & Ageing volume 8, Article number: 2 (2011)
The age- and cytomegalovirus (CMV)-seropositivity-related changes in subsets and differentiation of circulating T cells were investigated in end-stage renal disease (ESRD) patients (n = 139) and age-matched healthy individuals. The results show that CMV-seropositivity is associated with expansion of both CD4+ and CD8+ memory T cells which is already observed in young healthy individuals. In addition, CMV-seropositive healthy individuals have a more differentiated memory T cell profile. Only CMV-seropositive healthy individuals showed an age-dependent decrease in CD4+ naïve T cells. The age-related decrease in the number of CD8+ naïve T cells was CMV-independent. In contrast, all ESRD patients showed a profound naïve T-cell lymphopenia at every decade. CMV-seropositivity aggravated the contraction of CD4+ naïve T cells and increased the number of differentiated CD4+ and CD8+ memory T cells. In conclusion, CMV-seropositivity markedly alters the homeostasis of circulating T cells in healthy individuals and aggravates the T cell dysregulation observed in ESRD patients.
End-stage renal disease (ESRD) is associated with an immune defect characterized by increased susceptibility for infections and decreased humoral responses to T-cell dependent antigens like HBsAg [1, 2]. Circulating T lymphocytes can be dissected into subsets of naïve and memory T lymphocytes using the common leukocyte antigen CD45RO (memory marker) and the chemokine receptor CCR7 which is important for homing of T cells to lymphoid organs. Differential expression of CD45RO and CCR7 allows for further dissection of functionally different T lymphocyte subsets; naïve T cells (Tnaive, expressing CCR7), central-memory T cells (Tcm, expressing CCR7) and effector-memory (Tem, no expression of CCR7) . In addition, within the CD8+ T lymphocyte subset an extra late effector memory population can be distinguished, lacking both CCR7 and CD45RO (Temra) [4, 5]. The loss of expression of the co-stimulatory molecule CD28 and increased expression of CD57 on memory T cells is indicative of a later stage of differentiation of T cells with diminished replicative capacity .
Progressive loss of renal function is associated with a progressive decrease in the size of the the naïve T cell compartment, a decrease within CD4+ Tcm lymphocytes and a significant increase in CD8+ Temra [7, 8]. In addition, we have demonstrated that the severely impaired humoral response of ESRD patients to HBV vaccination can be attributed to a specific deficit in the generation of antigen-specific effector-memory CD4+ T cells . Therefore, the disturbed composition of circulating T cells in ESRD patients seems to underly, at least partly, their immune deficiency.
Cytomegalovirus (CMV) seropositivity is known to have a major impact on the repertoire of antigen specific T cells as an estimated 10% of circulating T cells is CMV-antigen specific in seropositive individuals . In addition, the changes generally observed with an aged immune system, like a decreased CD4/CD8 ratio and expansion of CD28 negative CD8+ positive T cells seem to be related to CMV seropositivity [11–13]. The prevalence of CMV seropositivity increases with age and varies with socio-economic and ethnic background from 30 to 100% . Therefore, any analysis of age-related changes of the immune system should take CMV-seropositivity into account. To date few studies have documented the interaction between CMV-seropositivity and ageing on the absolute numbers of circulating T cell subsets in healthy controls [11, 15, 16]. Although these studies indicated an CMV-related increase in total numbers of CD8+ T cells, they reached dissimilar conclusions with respect to CMV-related changes of T cells at young age which may be due to differences in definition of the various T cell populations.
ESRD patients have increased numbers of circulating CD8+ Temra cells and CD28 negative T cells suggesting a major influence of CMV seropositivity on T cell immunity . However, it is not known how CMV and ageing interact and contribute to the observed ESRD-related changes in numbers of circulating T cells subsets. A carefull dissection of the influence of these different factors (loss of renal function, age and CMV seropositivity) on circulating T cells is pivotal to understand the ESRD-related immune deficiency.
To examine this question, we have performed a large cross-sectional study including ESRD patients and healthy donors.
Material and methods
Patients aged 18 to 78 years were recruited for the study from our outpatient clinic for renal transplantation during a period of 2.5 years. All patients had ESRD, defined as an estimated glomerular filtration rate of less then 15 mL/min with or without renal replacement therapy. Patients with a malignancy, active infection or taking immunosuppressive drugs were excluded. The healthy individuals were recruited from their relatives, thereby matching for socio-economic and ethnical background. All patients and healthy controls included gave informed consent and the local medical ethical committee approved the study. It was conducted according to the principles of Declaration of Helsinki and in compliance with International Conference on Harmonization/Good Clinical Practice regulations. Study population characteristics are depicted in Table 1. We aimed at 5 to 10 CMV-seropositive and -seronegative individuals at each age-decade.
Flowcytometric analysis of the various T lymphocyte subsets
To determine the percentages and absolute numbers of the various T lymphocytes, we performed a whole blood staining as described previously but with some minor adjustments . Briefly, to distinguish the various T lymphocyte subsets, we used AmCyan-labelled CD3 (BD, Erembodegem, Belgium) with either peridinin chlorophyll protein (PerCP)-labelled CD4 or CD8 in combination with allophycocyanin (APC)-labelled CD45RO (BD) or Pacific Blue-labelled CD45RO (Biolegend Europe B.V, Uithoorn, Netherlands), and fluorescein isothiocyanate (FITC)-labelled CCR7 (R&D Systems Europe Ltd, Abingdon, UK). The various subsets are defined as CD4+ or CD8+ and either naive being CCR7+ CD45RO- (Tnaive) or belonging to the memory population (Tmem). The latter can be further dissected in central memory being CCR7+ CD45RO+ (Tcm), effector memory being CCR7-CD45RO+ (Tem) and for the CD8+ T lymphocytes, Temra being CCR7- CD45RO-. In addition, percentages of CD28- (CD28null) and CD57+ for CD4+ and CD8+ T lymphocytes were determined using phycoerythrin (PE)-labelled CD28 (BD) and APC-labelled CD57 (Biolegend), respectively. For each measurement, we acquired 50000 lymphocytes to ensure reliable results. Analysis was performed using the FACS Canto™ II (BD) and FACSDIVA software (BD).
Serum IgG antibodies to CMV were measured with an enzyme immuno assay (Biomerieux, VIDAS, Lyon, France) and expressed as arbitrary units/ml (AU/mL). Following the manufacturers guidelines, a test result exceeding 6 AU/mL was considered positive for the presence of CMV-specific IgG antibodies.
The non-parametric Spearman's rank correlation (Rs) test was performed to analyze correlations between age and the various T lymphocytes subsets in the group of healthy individuals and ESRD patients. ESRD patients and their age-matched healthy controls were divided into two groups; 20-40 years (young) and 60-80 years (old), to evaluate the effect of CMV seropositivity on the composition of the T lymphocyte compartment. The Mann-Whitney U-test was used to compare values between CMV-seronegative and seropositive individuals as well as to compare ESRD patients to healthy donors. Distribution of gender and CMV-seropositivity was tested using the Chi-square test. P-values less than 0.05 were considered significant. The SPSS software version 17 was used for all statistical tests.
CMV-seropositivity is associated with increased T cell numbers and differentiation to a memory-effector phenotype in healthy young individuals
At young age, the absolute number of CD4+ and CD8+ T cells was increased in CMV-seropositive healthy individuals by 76% and 83%, respectively when compared to CMV-seronegative healthy individuals (Table 2). Both the naïve and memory T cells showed increased cell numbers, although the memory compartment contributed for the largest part (48% for CD4+ and 64% for CD8+ T lymphocytes). In both CD4+ and CD8+ T memory cells a significant increase in differentiation towards the effector-memory phenotype was observed. Within the memory compartment, the CD4 Tem increased by 2.1-fold and the CD8 Tem by 1.5-fold. The memory CD8+ T cells showed the highest degree of differentiation to an effector phenotype as the Temra cells were on average 2.3-fold increased in CMV-seropositive healthy donors (Table 2).
CMV-seropositivity selectively influences T cell subsets with increasing age
With increasing age, the CD4+ T lymphocyte population and the different subsets remained remarkably unaffected in CMV-seronegative persons over a period of 4 to 5 decades (Figure 1B and Figure 2A-D, straight line). However, in CMV-seropositive healthy individuals the elevated CD4 T cell numbers at young age, specifically the Tnaive, decreased to values similar to seronegative persons at old age (Table 2 Figure 1B and Figure 2A, dotted line).
The findings were very different for age-related changes of CD8+ T cells. Most notably, a steep decrease (> 80%) was observed in Tnaive cell numbers which was unaffected by CMV- seropositivity. In CMV-seronegative individuals this resulted in a modest decrease of the total CD8+ T cell population, as the Tmem remained unchanged with increasing age (Table 2). In CMV-seropositive individuals the CD8+ Tmem increased significantly (P = 0.02) with increasing age (Figure 3E), an effect which could be observed in all memory subpopulations although statistical significance was not reached (Figure 3B-D). This resulted in a significantly age-related decrease in the CD4/CD8 ratio (P < 0.01) in CMV-seropositive healthy individuals, but not in CMV seronegative individuals (data not shown).
Impact of CMV-seropositivity on composition of T lymphocytes subsets in ESRD patients
Compared to CMV-seropositive healthy individuals, ESRD patients have a significantly (P < 0.01) lower number of T lymphocytes which is related to a relative CD4+ T cell lymphopenia at all ages. The decreased CD4+ T cell numbers are caused by a significant decrease in Tnaive and Tcm as has been described before . The CD4+ Tnaive decreased with increasing age but this association was only statistically significant (P < 0.01) in CMV-seropositive patients (Figure 2E), and resulted in a significantly (P = 0.03) lower number of Tnaive at old age in CMV-seropositive patients (Table 3).
Similar as observed in healthy individuals, the CD4+ T memory compartment (Figure 1E) and its subsets (Figure 2E-H) remained stable with age, irrespective of CMV-serostatus. The influence of CMV-seropositivity on differentiation to an effector memory phenotype was less clear in ESRD patients, compared to healthy individuals.
The CD8+ Tnaive population showed a very significant age-related decrease, irrespective of CMV-serostatus and with a similar slope as healthy individuals. At all ages, CD8+ T lymphocytes of CMV-seropositive ESRD patients are significantly higher due to an increased Tmem when compared to their seronegative counterparts similar to healthy donors. The Tmem does not increase with age (Figure 3J) as was observed for CMV-seropositive healthy individuals. At young age, CD8+ Temra and Tmem are approximately 6- and 1.6-fold increased whereas at old age the values are 5.5- and 1.7-fold (Table 3). The decrease of Tnaive cell numbers but unchanged Tmem subsets led to a significant age-related decrease of total CD8+ T cell numbers in ESRD patients (Figure 1F).
CMV seropositivity and ESRD increase CD57 expression and loss of CD28 on memory T cells
Markers specific for terminal differentiation of T lymphocytes, i.e. loss of CD28 expression (CD28null) and percentages CD57+ T lymphocytes are specifically higher within CD4+ Tmem of CMV-seropositive healthy individuals. Similar results were obtained for percentages of CD28null, but not CD57+, Tmem cells within the CD8+ T lymphocyte compartment. With increasing age, these markers remained stable (Table 2).
Similar to the healthy counterparts, significantly higher percentages of CD28null and CD57+ in both CD4+ and CD8+ Tmem lymphocytes were observed in CMV-seropositive ESRD patients (Table 3). Moreover in contrast to healthy donors, a significant increase in percentages of CD28null CD4+ Tmem was observed when old ESRD patients were compared to young ones (Table 3, 11.9% to 4.0%, p < 0.001). Also, the percentage of CD57 positive CD4+ Tmem was significantly higher in CMV-seropositive ESRD patients as compared to healthy controls (at young age 34.0% versus 18.1% and at old age 35.7% versus 13.2% for CMV-seropositive ESRD patients and CMV-seropositive healthy donors, respectively, p < 0.01.)
In this study we have analyzed the differential and combined effects of age, CMV latency and loss of renal function on numbers and composition of the various T lymphocytes. The results show that CMV latency, defined by CMV seropositivity, has a major impact on circulating T cell numbers, composition and age-related effects of the immune system. Moreover, CMV aggravates some pre-existing changes in the T cell compartment of ESRD patients.
A remarkably stable composition of the CD4+ T cell compartment was noted in CMV-seronegative healthy donors over an age span of at least 5 decades. Both total number of CD4+ T cells and relative distribution remained unchanged in the elderly population. In contrast, the CD8+ naive T cell subset showed a major age-related decline while the memory compartment remained stable with respect to differentiation and expressing of ageing markers CD28null and CD57. The preferential age-related decrease of CD8 Tnaive cells is in accordance with previous studies  and, although speculative, may be caused by a higher antigen driven turnover of these cells as compared to CD4+ T naive cells.
CMV-seropositivity has a large effect on CD4+ and CD8+ T cell subsets at all ages in healthy individuals. It is associated with increased numbers of all CD4+ T cells at young age and smaller numbers at old age, in particular within the Tnaive cell subset.
CMV-seropositivity was associated with a different effect on CD8+ T cells, as only the memory T cell compartement was significantly and stably expanded. The slope of the age-related decline of CD8 Tnaive was not affected by CMV-seropositivity. Confirming previous results, the appearance of CD28null cells within the CD4+ Tmem cell compartment seemed pathognomonic for CMV-seropositivity, but was unaffected by increasing age [15, 17, 19]. Overall, the results indicated that loss of CD28 expression and increased expression of CD57 on CD4+ and CD8+ T cells was highly associated with CMV-seropositivity. These markers should therefore be interpretated with care in clinical studies that study the ageing of T cells, taking into account the potential confounder of increasing prevalence of CMV-seropositivity with age. Hypothetical extrapolation of the regression lines of the total CD4+ and CD8+ T cell (sub) populations beyond 80 years results in a lowered CD4/CD8 T cell ratio, lowered Tnaive cell numbers and an increased percentage of memory T cells with a higher percentage of CD28null cells. These findings have indeed been described in the healthy very old and specifically in relation with CMV-seropositivity [11, 20, 21]. Therefore, it seems likely that the changes seen in the age span from 20 to 80 years continue within the ninth and tenth decade. The CMV-seropositivity related changes of the T cell immune system at old age are associated with an increased risk for mortality and therefore seem to be of clinical significance. Destabilization of atherosclerotic plaques by CD4+CD28null T cells  or immune suppressor activity of CD8+CD28null T cells [22, 23] may explain this increased risk for mortality in elderly CMV-seropositive individuals.
The age-related decrease in the number of CD4+ and CD8+ Tnaive cells with CMV-seropositivity explains the reported age-related increased of memory T cells when percentages and not absolute numbers of cells are used . However, studies involving human subjects that have reported absolute numbers of circulating T cell subsets in relation to age and CMV seropositivity are scarce [15, 16]. As our results clearly show, latency for CMV is associated with a stable increase of memory CD8+ T cells and an increase of memory CD4+ T cells at young age. This is in sharp contrast to the results from the study by Chidrawar , which may be explained by the relative low number of young CMV-seropositive individuals in this study, but similar to data obtained by Looney et al..
It is known that CMV antigen-specific T cells may be present at a high frequency within the pool of circulating CD4+ and CD8+ T cells [25, 26], but our results are not in support of a limited immunological space [24, 27] but actually show expansion of the T cell population under influence of CMV latency. The relative large CMV-related increase in total T cell numbers (> 30%) indicate a bystander effect on other T cells  which is in accordance with the discrepancy noted between e.g. the percentage of CMV-specific CD4+ T cells and the higher percentage of CD4+CD28null cells [17, 28].
In addition to the pleiotropic effects of CMV-seropositivity on T cell subsets in relation with age, the effects in ESRD patients are again different. ESRD patients have a remarkable contracted population of naive CD4+ and CD8+ T cells at all ages. The causes of this Tnaive lymphopenia are not certain but may involve reduced thymic output, lack of IL-7 and increased activation-induced apoptosis in ESRD patients [7, 8]. Most strikingly, the association between CMV-seropositivity and increased expansion of CD4+ T cells at young age was not observed in ESRD patients. In addition, independent of CMV-seropositivity an age-related progressive decline of an already contracted naive CD4+ T cell at young age was observed. However, CMV-seropositivity showed an add-on effect on CD4+ Tnaive lymphopenia and was associated with the development of terminally differentiated effector-memory T cells in both the CD4+ and CD8+ compartment. Similar to healthy individuals, the appearance of CD28null T cells and increased CD57 expression was highly associated with CMV seropositivity. In CMV-seropositive ESRD patients, the percentage of CD57 positive cells was significantly higher and the percentage of CD4+CD28null T cells increased with age. Overall, CMV-seropositivity aggravates the ESRD-related changes of the T cell immune system.
A unifying hypothesis may be that frequent CMV reactivation , [30, 31] causes a lifetime activation of the immune system with an initial increase of CD4+ T cells at young age but over the years exhaustion of replicative capacity with progressive decrease of naive T cells [32–34]. In ESRD a similar process occurs with continuous T cell activation possibly by the pro-inflammatory state of uremia and increased susceptibility for activation induced cell death. The net effect is severe Tnaive cell depletion and increased numbers of terminally differentiated CD4+ and CD8+ memory T cells which is aggravated by CMV reactivation. CMV reactivation is triggered by inflammatory stimuli creating the possibility that the pro-inflammatory condition of ESRD patients leads to more frequent subclinical CMV reactivation and even CMV disease [14, 35].
The negative association of an CMV associated immune risk profile with survival in the very old is known and is likely also of clinical importance, but at a much earlier age, in ESRD patients. Understanding the combined effects of age, CMV seropositivity and ESRD on T cell immunity may help to identify patients at risk for a decreased vaccination response [36, 37], at risk for cardiovascular events , and may guide patient-tailored immune suppression after kidney transplantation .
Conflict of interest statement
The authors declare that they have no competing interests.
Descamps-Latscha B, Herbelin A, Nguyen AT: Balance between IL-1 beta, TNF-alpha, and their specific inhibitors in chronic renal failure and maintenance dialysis. Relationships with activation markers of T cells, B cells, and monocytes. J Immunol. 1995, 154 (2): 882-92.
Verkade MA, van de WJ, Klepper M, Vaessen LM, Weimar W, Betjes MG: Peripheral blood dendritic cells and GM-CSF as an adjuvant for hepatitis B vaccination in hemodialysis patients. Kidney Int. 2004, 66 (2): 614-21. 10.1111/j.1523-1755.2004.00781.x.
Sallusto F, Geginat J, Lanzavecchia A: Central memory and effector memory T cell subsets: function, generation, and maintenance. Annu Rev Immunol. 2004, 22: 745-63. 10.1146/annurev.immunol.22.012703.104702.
Geginat J, Lanzavecchia A, Sallusto F: Proliferation and differentiation potential of human CD8+ memory T-cell subsets in response to antigen or homeostatic cytokines. Blood. 2003, 101 (11): 4260-6. 10.1182/blood-2002-11-3577.
Sallusto F, Lenig D, Forster R, Lipp M, Lanzavecchia A: Two subsets of memory T lymphocytes with distinct homing potentials and effector functions. Nature. 1999, 401 (6754): 708-12. 10.1038/44385.
Appay V, van Lier RA, Sallusto F, Roederer M: Phenotype and function of human T lymphocyte subsets: consensus and issues. Cytometry A. 2008, 73 (11): 975-83.
Litjens NH, van Druningen CJ, Betjes MG: Progressive loss of renal function is associated with activation and depletion of naive T lymphocytes. ClinImmunol. 2006, 118 (1): 83-91.
Yoon JW, Gollapudi S, Pahl MV, Vaziri ND: Naive and central memory T-cell lymphopenia in end-stage renal disease. Kidney Int. 2006, 70 (2): 371-6. 10.1038/sj.ki.5001550.
Litjens NH, Huisman M, van den Dorpel M, Betjes MG: Impaired immune responses and antigen-specific memory CD4+ T cells in hemodialysis patients. J Am Soc Nephrol. 2008, 19 (8): 1483-90. 10.1681/ASN.2007090971.
Sylwester AW, Mitchell BL, Edgar JB: Broadly targeted human cytomegalovirus-specific CD4+ and CD8+ T cells dominate the memory compartments of exposed subjects. J Exp Med. 2005, 202 (5): 673-85. 10.1084/jem.20050882.
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 (2-3): 445-53. 10.1016/S0531-5565(01)00212-1.
Sauce D, Larsen M, Fastenackels S: Evidence of premature immune aging in patients thymectomized during early childhood. J Clin Invest. 2009, 119 (10): 3070-8. 10.1172/JCI39269.
Derhovanessian E, Larbi A, Pawelec G: Biomarkers of human immunosenescence: impact of Cytomegalovirus infection. Curr Opin Immunol. 2009, 21 (4): 440-5. 10.1016/j.coi.2009.05.012.
Betjes MG, Litjens NH, Zietse R: Seropositivity for cytomegalovirus in patients with end-stage renal disease is strongly associated with atherosclerotic disease. NephrolDialTransplant. 2007, 22 (11): 3298-303.
Looney RJ, Falsey A, Campbell D: Role of cytomegalovirus in the T cell changes seen in elderly individuals. Clin Immunol. 1999, 90 (2): 213-9. 10.1006/clim.1998.4638.
Chidrawar S, Khan N, Wei W, McLarnon A, Smith N, Nayak L, Moss P: Cytomegalovirus-seropositivity has a profound influence on the magnitude of major lymphoid subsets within healthy individuals. Clin Exp Immunol. 2009, 155 (3): 423-32. 10.1111/j.1365-2249.2008.03785.x.
Betjes MG, Huisman M, Weimar W, Litjens NH: Expansion of cytolytic CD4+CD28- T cells in end-stage renal disease. Kidney Int. 2008, 74 (6): 760-7. 10.1038/ki.2008.301.
Fagnoni FF, Vescovini R, Passeri G: Shortage of circulating naive CD8(+) T cells provides new insights on immunodeficiency in aging. Blood. 2000, 95 (9): 2860-8.
Gamadia LE, Rentenaar RJ, Baars PA: Differentiation of cytomegalovirus-specific CD8(+) T cells in healthy and immunosuppressed virus carriers. Blood. 2001, 98 (3): 754-61. 10.1182/blood.V98.3.754.
Naylor K, Li G, Vallejo AN: The influence of age on T cell generation and TCR diversity. J Immunol. 2005, 174 (11): 7446-52.
Wikby A, Maxson P, Olsson J, Johansson B, Ferguson FG: Changes in CD8 and CD4 lymphocyte subsets, T cell proliferation responses and non-survival in the very old: the Swedish longitudinal OCTO-immune study. Mech Ageing Dev. 1998, 102 (2-3): 187-98. 10.1016/S0047-6374(97)00151-6.
Effros RB: Role of T lymphocyte replicative senescence in vaccine efficacy. Vaccine. 2007, 25 (4): 599-604. 10.1016/j.vaccine.2006.08.032.
Suzuki M, Konya C, Goronzy JJ: CM Weyand. Inhibitory CD8+ T cells in autoimmune disease. Hum Immunol. 2008, 69 (11): 781-9. 10.1016/j.humimm.2008.08.283.
Weinberger B, Lazuardi L, Weiskirchner I: Healthy aging and latent infection with CMV lead to distinct changes in CD8+ and CD4+ T-cell subsets in the elderly. Hum Immunol. 2007, 68 (2): 86-90. 10.1016/j.humimm.2006.10.019.
Harari A, Zimmerli SC, Pantaleo G: Cytomegalovirus (CMV)-specific cellular immune responses. Hum Immunol. 2004, 65 (5): 500-6. 10.1016/j.humimm.2004.02.012.
Maecker HT, Maino VC: Analyzing T-cell responses to cytomegalovirus by cytokine flow cytometry. HumImmunol. 2004, 65 (5): 493-9.
Franceschi C, Bonafe M, Valensin S: Human immunosenescence: the prevailing of innate immunity, the failing of clonotypic immunity, and the filling of immunological space. Vaccine. 2000, 18 (16): 1717-20. 10.1016/S0264-410X(99)00513-7.
Gamadia LE, Remmerswaal EB, Weel JF, Bemelman F, van Lier RA, Ten Berge IJ: Primary immune responses to human CMV: a critical role for IFN-gamma-producing CD4+ T cells in protection against CMV disease. Blood. 2003, 101 (7): 2686-92. 10.1182/blood-2002-08-2502.
Hummel M, Abecassis MM: A model for reactivation of CMV from latency. J Clin Virol. 2002, 25 (Suppl 2(2)): S123-36. 10.1016/S1386-6532(02)00088-4.
Stowe RP, Kozlova EV, Yetman DL, Walling DM, Goodwin JS, Glaser R: Chronic herpesvirus reactivation occurs in aging. Exp Gerontol. 2007, 42 (6): 563-70. 10.1016/j.exger.2007.01.005.
Glaser R, Kiecolt-Glaser JK: Stress-induced immune dysfunction: implications for health. Nat Rev Immunol. 2005, 5 (3): 243-51. 10.1038/nri1571.
van de Berg PJ, Griffiths SJ, Yong SL: Cytomegalovirus infection reduces telomere length of the circulating T cell pool. J Immunol. 2010, 184 (7): 3417-23. 10.4049/jimmunol.0903442.
Shin H, Wherry EJ: CD8 T cell dysfunction during chronic viral infection. Curr Opin Immunol. 2007, 19 (4): 408-15. 10.1016/j.coi.2007.06.004.
Mueller SN, Ahmed R: High antigen levels are the cause of T cell exhaustion during chronic viral infection. Proc Natl Acad Sci USA. 2009, 106 (21): 8623-8. 10.1073/pnas.0809818106.
Hahn G, Jores R, Mocarski ES: Cytomegalovirus remains latent in a common precursor of dendritic and myeloid cells. Proc Natl Acad Sci USA. 1998, 95 (7): 3937-42. 10.1073/pnas.95.7.3937.
Goronzy JJ, Fulbright JW, Crowson CS, Poland GA, O'Fallon WM, Weyand CM: Value of immunological markers in predicting responsiveness to influenza vaccination in elderly individuals. J Virol. 2001, 75 (24): 12182-7. 10.1128/JVI.75.24.12182-12187.2001.
Trzonkowski P, Mysliwska J, Szmit E, Wieckiewicz J, Lukaszuk K, Brydak LB, Machala M, Mysliwski A: Association between cytomegalovirus infection, enhanced proinflammatory response and low level of anti-hemagglutinins during the anti-influenza vaccination--an impact of immunosenescence. Vaccine. 2003, 21 (25-26): 3826-36. 10.1016/S0264-410X(03)00309-8.
Trzonkowski P, Debska-Slizien A, Jankowska M: Immunosenescence increases the rate of acceptance of kidney allotransplants in elderly recipients through exhaustion of CD4+ T-cells. Mech Ageing Dev. 2010, 131 (2): 96-104. 10.1016/j.mad.2009.12.006.
NL designed the study, performed the experiments, statistical analyses and drafted the manuscript, EdW performed the experiments and MB designed the study and drafted the manuscript. All authors read and approved the final manuscript.
About this article
Cite this article
Litjens, N.H., de Wit, E.A. & Betjes, M.G. Differential effects of age, cytomegalovirus-seropositivity and end-stage renal disease (ESRD) on circulating T lymphocyte subsets. Immun Ageing 8, 2 (2011). https://doi.org/10.1186/1742-4933-8-2
- Lymphocyte Subset
- ESRD Patient
- Increase CD57 Expression
- Memory Compartment
- Immune Risk Profile