Immunosenescence and gender: a study in healthy Cubans
The progressive decline in the immune function during ageing is termed immunosenescence. Previous studies have reported differences between males and females in the distribution and cell responses of lymphocyte subsets. Most studies of immunosenescence have been done in populations of industrialized countries living in a rather cold environment, and facing lower antigenic challenges such as Cytomegalovirus (CMV). The aim of this study was to determine the effect of ageing on lymphocytes in a population with a high prevalence of CMV infection in all ages, and to compare gender differences related to the immunosenescence markers.
Different populations of peripheral blood leukocytes from healthy young and old IgG-CMV seropositive individuals were examined using flow cytometry. With age, the number and frequency of B cells and T cells significantly decreased, while highly differentiated T cells increased. Such changes were different in males and females. The age-associated decline of less differentiated lymphocyte subsets (CD19, CD4 and CD8 cells) and the increase of highly differentiated T cells were more prominent in females. In males, there were no significant changes in CD19, CD4 and CD8 subsets but there was a significant increase in the proportion of highly differentiated T cells.
Shifts in lymphocyte subsets distribution were influenced by age and gender in an IgG-CMV seropositive population. These results suggest different patterns of immunosenescence in respect to gender differences. These patterns could have implications in the design of immunotherapy in the elderly.
KeywordsEpstein Barr Virus Total Lymphocyte Count Thymus Involution Seropositive Individual Antigenic Load
White blood cells
Peripheral blood Lymphocytes.
The function of the immune system declines with age leading to increased susceptibility to infectious diseases, cancer and poor response to vaccination [1, 2]. This decline is termed “Immunosenescence” .
Immunosenescence is related to thymus involution, reduction in the generation of naïve T-cell populations, changes in the peripheral T lymphocyte compartments and reduced functional immune competence. The nature of these changes is associated with exposure to environmental challenges, such as stress and pathogens .
Age-associated changes in lymphocyte subpopulations have been documented in diverse contexts. The Swedish octogenarian study (OCTO-immune), showed an increasing number of individuals with CD4:CD8 ratio less than 1, driven by the decrease in CD4 T cell subsets and/or expansion of CD8 T cells. The increase in CD8 and its relationship with cytomegalovirus (CMV) infection suggest that the infection with this virus might be a contributor to this significant expansion of CD8 T cells .
In Britain, Akbar and coworkers identified the progressive stages in T cell differentiation by sequential changes in the expression of surface markers, such as CD45RA, CD28, CD27, and CCR7 . The proportion of most differentiated T cells in both CD4+ and CD8+ populations, were designated as CD28-, CD27-, CCR7- by another group in France .
Age-related changes in CD4 T cells have been less documented than in CD8 cells. However, there is also evidence of an increase of CD45RA+CD27-CD4+ T cells in older subjects , especially in CMV-infected subjects. These cells are mostly CMV-specific, but there is also an increase in effector CD4+ T cells that are specific for other viruses, i.e. EBV, HSV, and VZV .
One of the fundamental manifestations of immunosenescence is a steady decrease of functional thymus tissue which begins after birth, accelerates with puberty and is almost completed by the age of 50 [9, 10]. A dramatic decline in peripheral naïve T cells in both, CD4+ and CD8+ subsets, have been observed in elder people . The kinetics of thymus involution could be related to the genetic background of human populations and is also influenced by sex hormones, such as estrogen and testosterone. The thymus made fewer new cells with age in both sexes, but women still had higher levels of new T cells than men of the same age . Epidemiological differences between sexes (such as weight, lifestyle, smoking, and medication) could also account for differences observed .
Additionally, immunosenescence is at least partially driven by the chronic antigenic load, which is obviously different in diverse environments. These facts support the hypothesis that the kinetics of immunosenescence could be different in each country and therefore should be characterized in every specific context as part of the information needed for a scientifically based public health policy, especially in countries with aged populations.
Most studies attempting to assess immunosenescence have focused on a single population, mostly “WEIRD” (ie Western, educated, industrialized, rich, democratic). These are not necessarily representative of the majority of the world’s population . There is a scarcity of data about immunosenescence in developing countries and tropical climate.
This article presents findings from a Cuban population study aimed to investigate the effect of age and gender on lymphocyte populations in healthy humans. Moreover, Cuba could become a kind of natural experiment providing one of the rare situations in which long life expectancy, low infant mortality and intensive vaccination coverage, typical of northern wealthy populations, are coincident with the high antigenic load of a tropical environment.
Prevalence of CMV-IgG seropositivity
CMV-IgG seropositivity was determined in all individuals (n=112). The overall prevalence of seropositive individuals was 90.1% ( n=101). Antibodies against CMV were found in more than 90% of old individuals no matter the gender. However in younger ages, there was a higher frequency of seropositive in males (93.3%) than in females (73.6%), although statistical significance was not achieved (Fisher test, p>0.05).
Eleven subjects (8 females and 3 males) distributed within both age groups, were CMV-IgG seronegatives. As a consequence of their low prevalence in each age/gender group, it was not possible to establish comparisons between seronegative and seropositive individuals in each group. In consequence, they were omitted in the subsequent analysis.
Significant decline of total lymphocyte counts with age in CMV seropositive Cubans is driven by the female group
No changes in the ratio of CD4+:CD8+ T cells with age were observed in the CMV seropositive individuals included in the previous analysis. None of the seronegative individuals showed inversion in the CD4+:CD8+ ratio. Within seropositive ones there was a low frequency of inversion (8.9%, n=9). A higher prevalence of an inverted CD4+:CD8+ ratio was found in the aged group (10.9% vs 3.6% in the youngest) and the highest frequency was observed in elder males. However, no significant differences were found applying a Fisher test.
Significant increase in the proportion of activated and differentiated CD8 T cells with age
Variation of terminally differentiated CD45RA+ CD28- T cells with age and gender
Cuban males showed a higher proportion of terminally differentiated T cells than females since youth ages. In fact, young males displayed higher frequencies of CD45RA+CD28- T cells than young females within both CD4+ (p=0.063) and CD8+ (p=0.015) T cell subsets (Mann Whitney test p<0.05). However in elder populations, significant differences (p=0.027) were found only within CD8+ T lymphocytes. Indeed, elder males had a higher frequency of CD8+CD45RA+CD28- than elder females (Figure 5C).
Changes in cells of the immune system related to age have been the subject of many studies in the last two decades [18, 19, 20, 21, 22].Most published studies document a decrease in the number and proportion of naïve CD8 T cells in aged individuals together with a reciprocal increase in memory CD8 T cells [4, 23]. These facts have been frequently associated to a seropositive response to CMV . There are also recent data showing a decline in peripheral naive CD4 T cells number with age  and a recent study showed that CMV infection significantly increases the proportion of effector memory-like CD4+ T cells in elder humans .
Another study of 1,468 community-dwelling elderly Latinos, showed that increasing CMV IgG antibody titers were associated with the overall cause of mortality even after adjusting for various covariates such as age, gender, education, and baseline health conditions . The CMV persistent infection has been considered as one of the major drivers of immunosenescence  and such study also contributes to the growing evidence that CMV immune response is related to the deleterious processes involved in aging.
The hallmarks of immunosenescence would be affected by the history of the individual’s exposure to pathogens . The Cuban population could be a particular case worth to study, where exceptionally the high antigenic load typical of a developing country in the tropical belt is coincident with low infant mortality, high life expectancy  and an aged demographic pyramid , as a consequence of social interventions.
The high prevalence of CMV infection in tropical countries has been attributed to several sociocultural behaviors that may predispose to increased transmission of human CMV in early ages of life . A high prevalence of seropositivity to cytomegalovirus in Cubans, after hemodialysis, HIV infection and renal transplants has been previously described [30, 31, 32]. The present study is the first one to evaluate the immunosenescence markers in Cubans. We also confirmed a high seroprevalence of CMV infection in our population since young ages, but in this case in healthy individuals.
We found age-associated decreases in the counts of total lymphocytes, both in B (CD19+) and T cells (CD4+ and CD8+ T cells). These findings are very similar to previous results showing a significant decline of total lymphocytes with age  as a consequence of the contraction of T  and B cell populations . In addition, we found gender differences consisting of a significant decline in the lymphocytes number with age, in females, and not in males.
Differences in the immune system functioning in males and females have been previously described [36, 37]. Such differences may occur due to the opposing ways in which hormones act [38, 39]. In fact, Th1 and Th2 responses appear affected by androgenic and estrogenic preponderance, respectively. While androgens favor the development of a Th1 response and the activation of CD8 cells ; estrogens seem to direct the immune system towards a Th2 dominance, where B lymphocytes are activated . Those findings are in line with the higher levels of B cells found in Cuban females, and in the increased frequency of differentiated CD8 T cells in males since young ages.
Furthermore, hormonal differences seem the most probable cause of gender-related changes in the rate of thymus involution. Male sexual hormones have been shown to accelerate thymus involution more profoundly than female hormones, according to reports of improved thymus function in male gonadectomized mice . While the thymus made fewer new cells with age in both sexes, women still had higher levels of new T cells than men of the same age . Epidemiological differences between the sexes (such as weight, lifestyle, smoking, and medication) could also account for the differences observed . In addition, several studies in mice showed a more vigorous humoral and cellular immune responses in females than in males [42, 43], and a superior ability of females to fight infections [44, 45]. All these findings are in line with our results on gender differences in B and T cell compartments.
In our study the main markers of immunosenescence in CMV seropositive males were those related to the proportion of CD8 differentiated T cells. The age-associated increase in the proportion of CD8+/CD57+ cells, expressing down modulation of cytotoxic activity, and in terminally differentiated CD8+/CD28- T cells were only observed in males. Lenkei and Andersson reported a correlation of CMV antibody titers with lymphocyte activation status and CD57+ expression . Some studies from Merino et al. reported that expansion of CD8+CD57+CD28- cells was related to age, and also to CMV carrier status possibly related to repeated antigenic stimulation . However these previous studies did not report influence of gender on differentiation markers.
Additionally, It is known that during ageing and after CMV infection there is an increase of highly differentiated CD45RA re-expressing T cells within both the CD4 and CD8 compartments [48, 49, 50], This observations may reflect the impact of thymic involution compounded with persistent CMV infection during ageing . We also found increasing proportions of terminally differentiated CD8+/CD45RA+/CD28- T cells with age, but only significant in females, while males showed a higher proportion of these cells compared to females of young ages. Concerning terminally differentiated CD4 T lymphocytes, the results showed an age-associated increase in both sexes and a higher proportion of CD4+/CD45RA+/CD28- T cells also in males.
There have been many studies on the CMV-specific CD8+ T cell population [24, 51, 52, 53] and some about the characteristics of CMV-specific CD4+ T cells describing the impact that CMV infection has in shaping the T cell pool [11, 54, 55]. The majority of highly differentiated T cell populations in CMV-infected subjects are CMV specific but there are also increased numbers of these effector T cells that are specific for other viruses, i.e. EBV, HSV and VZV . This put forward that CMV infection may drive a global increase in T cell differentiation suggesting a bystander phenomenon . Alternatively, this could be due to an epidemiological coincidence of infections with diverse viruses. This hypothesis deserves further testing in Cuban population where a high seroprevalence of herpesviruses (CMV, herpes simplex type 1 virus (HSV) and Epstein Barr virus(EBV) infection has been previously described [30, 31, 32, 56].
To our knowledge, the impact of gender in shaping the T cell pool in CMV infected healthy humans has not been described before. The lower proportion of CD45RA+ CD28- T cells (both CD4 and CD8) exhibited by females during young ages and the high frequency of highly differentiated CD8 T cells sustained since young ages in males, is probably linked to gender differences in the contribution of thymic emigrants to the peripheral T cell pool with age previously reported by different authors [57, 58, 59]. This is also shown by persistent higher values of signal-joint T cell receptor rearrangement excision circles (sjTREC) in females between the ages of 20 and 50, and suggesting that the thymic output is prolonged at higher levels in females as compared with males . On the other hand, a very recent and unpublished study in Cuban patients (including more than 50% of pediatric samples) with mononucleosis syndrome, found higher seroprevalence of CMV (>79%) and EBV (64,8%) than of HSV (author personal communication). Consequently with this finding, we think that a higher exposure to antigenic loads +since infancy in Cuban population could drive a premature immunosenescence. This phenomenon could occur essentially in males, which could be potentially less protected, since male sexual hormones have been shown to accelerate thymus involution more deeply than female hormones .
The gender contrast in our study, points to a conservation of the output of naive cells until advanced ages in females, and a higher impact of antigen-driven differentiation of T cells in males probably due to genetic and environmental factors related to the control of lifespan. In fact, recent findings indicate that gender is a major variable in the genetics of longevity, suggesting in turn that men and women follow different strategies to reach longevity [60, 61]. These gender differences in the immunosenescence process remain significant even inside a population with high prevalence of CMV seropositivity in both sexes. Future studies should include the analysis of naive T cells and TRECS in both gender groups.
In elder population the differences in gender were found mainly for the differentiated CD8+T cells, where males showed again the highest proportion. However, in general we found a broader spectrum of changes with age in females rather than in males. Conversely, other studies in humans showed that changes observed with ageing were more apparent in males [14, 15] but the evidences are statistically significant only for a decrease of CD8+ alpha beta T cells and for an increase of the effector memory cells (CD3+CD45RA-CCR7-) . Wikby et al examined immune parameters for the adult lifespan and some of their major findings were a higher frequency of individuals with an inverted CD4/CD8 ratio and lower levels of CD3+CD4+ and CD8+CD45RA+CCR7+ cells in men than in women . It should be noticed that these studies evaluated different markers, and targeted human populations with lower life-long antigenic load, which could explain such dissimilar results.
Gender differences in the performance of the immune system have been suggested long time ago by epidemiological evidences such as the higher incidence of autoimmune diseases in females, and atherosclerosis-related diseases (linked to chronic inflammation) in males. However, the interplay among hormones, immunity and inflammation is so complex that resists any simple mechanistic interpretation.
Cancer vaccine clinical trials from our own group have previously shown that age is related to the survival advantage conferred by therapeutic vaccination with an immunogenic preparation containing human Epidermal Growth Factor .
Our data, together with previous findings on the role of gender in the genetic determinants of longevity [61, 63] and the gender-specific age-related remodeling of the cytokine network  indicate the need for deeper studies on gender-specific immunosenescence phenotypes to further explore their impact on immunotherapy and the potential relevance for personalized medicine. Such studies in naive and treated cancer patients are currently ongoing.
Peripheral blood samples were collected from healthy volunteers by venipuncture.
Age and gender distribution of healthy volunteers
Individuals younger than 60 years old were defined as young (median age 34 years old); while individuals older than 60 years old were defined as elder (median age 77.5 years old).
White blood cells collection and staining for flow cytometry
Red cells were isolated from whole blood with lysing solution (NH4Cl, EDTA (tetrasodium), KHCO3). White blood cells (WBCs) were washed twice with Citometry solution (PBS, BSA, Azide 20%). Specific antibodies against CD3, CD4, CD8, CD19, CD45RA, CD28 and CD57 molecules, conjugated either to FITC, PE and Cy5, were purchased from Serotec and used for staining.
For surface staining, WBCs (1 × 105 cells in 100 μL Citometry solution) were incubated with 1 μL of the antibody in the dark at 4°C for 20 min. Subsequently, cells were washed twice and analyzed on a three-color flow cytometer (FACS Scan), with gating on the total lymphoid populations. Samples were obtained and studied individually. All the data generated was obtained from fresh samples.
Serum IgG antibodies to CMV were measured with an enzyme immunoassay (ETI-CYTOK-G PLUS P002033, DiaSorin) and expressed as arbitrary units/ml (UI/mL). A tested result higher than 0.4 UI/mL was considered positive for the presence of CMV-specific IgG antibodies, as per the manufacturer’s guidelines.
The relationship between age in years and the absolute counts of cells with different cell surface markers was studied by linear regression analysis. Statistical significance between groups was evaluated using nonparametric Kruskal-Wallis test within One-way ANOVA or Mann Whitney test. Post hoc paired comparisons with Dunn’s Multiple Comparison Test were done for the variables that showed differences between groups after ANOVA analysis. All statistical analyses were performed with SPSS v15.0 and GraphPad 5. The statistical data were considered significant if p < 0.05.
We are grateful for the assistance of physician and nurses at Hogar Clínica San Rafael and Hogar Hermanas Giralt in the collection of blood samples of elderly individuals. Thanks to the younger volunteers from Center of Molecular Immunology. We are grateful also for the assistance of Professor Arne Akbar from UCL in UK, for his contribution to the design of this research. The authors thank Olga Gonzalez and Lila Castellano for the language corrections of the document.
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