Next Article in Journal
Induced Pluripotent Stem Cells for Tissue-Engineered Skeletal Muscles
Next Article in Special Issue
New Insights in Immunometabolism in Neonatal Monocytes and Macrophages in Health and Disease
Previous Article in Journal
Crosstalk of Inflammation and Coagulation in Bothrops Snakebite Envenoming: Endogenous Signaling Pathways and Pathophysiology
Previous Article in Special Issue
Increased Expression of Anaphylatoxin C5a-Receptor-1 in Neutrophils and Natural Killer Cells of Preterm Infants
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 24
Issue 14
10.3390/ijms241411511
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Sex Differences in the Frequencies of B and T Cell Subpopulations of Human Cord Blood

by
Michelle Bous
1,†,
Charline Schmitt
1,†,
Muriel Charlotte Hans
1,
Regine Weber
1,
Nasenien Nourkami-Tutdibi
1,
Sebastian Tenbruck
2,
Bashar Haj Hamoud
2,
Gudrun Wagenpfeil
3,
Elisabeth Kaiser
1,
Erich-Franz Solomayer
2,
Michael Zemlin
1 and
Sybelle Goedicke-Fritz
1,*
1
Department of General Pediatrics and Neonatology, Saarland University Medical Center, 66421 Homburg, Germany
2
Department of Gynaecology and Obstetrics, Saarland University Medical Center, 66421 Homburg, Germany
3
Institute for Medical Biometry, Epidemiology and Medical Informatics (IMBEI), Saarland University, Campus Homburg, 66421 Homburg, Germany
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2023, 24(14), 11511; https://doi.org/10.3390/ijms241411511
Submission received: 9 June 2023 / Revised: 5 July 2023 / Accepted: 12 July 2023 / Published: 15 July 2023
(This article belongs to the Special Issue Neonatal Immunology)
Browse Figures
Review Reports Versions Notes

Abstract

:
Cord blood represents a link between intrauterine and early extrauterine development. Cord blood cells map an important time frame in human immune imprinting processes. It is unknown whether the sex of the newborn affects the lymphocyte subpopulations in the cord blood. Nine B and twenty-one T cell subpopulations were characterized using flow cytometry in human cord blood from sixteen male and twenty-one female newborns, respectively. Except for transitional B cells and naïve B cells, frequencies of B cell counts across all subsets was higher in the cord blood of male newborns than in female newborns. The frequency of naïve thymus-negative Th cells was significantly higher in male cord blood, whereas the remaining T cell subpopulations showed a higher count in the cord blood of female newborns. Our study is the first revealing sex differences in the B and T cell subpopulations of human cord blood. These results indicate that sex might have a higher impact for the developing immune system, urging the need to expand research in this area.

1. Introduction

The development of the human immune system begins during intrauterine development and is not completed at birth [1]. Investigating sex differences in lymphocytes present in the cord blood essentially contributes to a deeper comprehension of the immune development in utero and of the potential consequences of these differences within the immune system. Although lymphocyte subpopulations evolve continuously and are influenced by environmental antigen exposure postpartum, analyzing the cord blood provides unique insights into the prenatal immune status and early immune imprinting before undergoing changes and adaptations.
The prenatal microenvironment contains information and signals that can shape immune development. These prenatal influences can affect the future reactivity, sensitivity, and functions of lymphocytes. The fetus learns to tolerate both self and maternal antigens, while simultaneously developing protective immunity in preparation for birth [2]. Epigenetic mechanisms, such as DNA methylation and histone demethylation, influence the gene expression patterns of lymphocytes during the prenatal stage and determine their future functionality [3,4,5].
After birth, many processes are initiated affecting the immune cells in particular due to changes in environmental antigen exposure [6,7]. Within the neonatal period, the immune system is immature and certain components of the adaptive immune response are not fully developed. Consequently, newborns are more prone to contracting infections due to their incomplete defense mechanisms against pathogens. The lack of immune memory leads to a limited protective immunity against infectious diseases, as they have only been exposed to a small range of pathogens [8]. In this context, viral and microbial colonization by perinatal transmission is of great importance in the maturation process of the innate and adaptive immune systems. Moreover, microbial dysbiosis within the first 100 days of life augments the risk of allergies during lifetime [9].
Moreover, there are notable differences in the antibody response of neonates when compared to adults. Although neonates benefit from maternal antibodies providing maternal passive immunity, their antibody titers are lower compared to adult blood [10,11].
During infancy, the immune system matures. As a continuous learning process, immunity is built up during pre-puberty by recurrent infections and vaccinations. With the onset of puberty, the immune system achieves similar functional capacities compared to a healthy, mature adult immune system [12].
The maturation of immune cells is a complex multi-layered process. Griffin et al. [13] described human B1 cells as a cluster of differentiation (CD) CD20+ CD27+ CD43+ B cell subpopulation based on the typical B1 functions observed in murine B1 cells: spontaneous immunoglobulin (Ig) IgM secretion, efficient T cell stimulation, and continuous intracellular signaling [13]. B1 cells have a huge percentage in the cord blood (CB) (50%) but decrease over the years [13,14].
Marginal zone B (MZ B cells) cells are non-circulating mature B cells which form an interface between blood and the lymph nodes [7,15]. Splenic MZ B cells, located in the marginal zone of the spleen, are part of the innate immune system responding to blood-borne antigens. MZ B cells only account for 5% of the innate and adaptive immune system; nevertheless, they are of utmost importance for early immune responses, interacting effectively with rapid antibody reactions on viral and bacterial pathogens [15].
Thymus-negative cells represent a premature stage of T helper (Th−) lymphocytes prior to the upcoming positive selection in the thymus. In the positive selection process, Th cells can bind major histocompatibility complexes (MHC) to receive positive growing signals and enter the cell cycle. Following the positive selection process, cells that bind to self-antigens are induced to apoptosis [16]. These selection processes take place in the thymus postnatally, assuming that the maturation of Th cells is not finished by the time of birth [17].
One important and long neglected fact are the differences between females and males. Investigating biological (sex) and sociocultural (gender) differences has gained more importance over the past few years. Within the field of medical research, most of the performed research and published data refers to male individuals. Sex differences have been found in certain diseases like asthma, diabetes, and cardiovascular disease. Women are at higher risk to develop diseases like Takotsubo cardiomyopathy, or show different manifestations of common diseases, like heart failure or myocardial infarction. Moreover, autoimmune diseases, such as systemic lupus erythematosus (SLE), multiple sclerosis (MS), rheumatoid arthritis, and Hashimoto’s thyroiditis are more common in women than in men [18,19].
To gain a deeper comprehension of the underlying causes of these sex-specific differences later in life, a profound investigation of these sex differences and their impact on early immune development is of utmost importance. Sex differences in immune responses can be mainly traced back to two main factors: the influence of sex hormones, such as testosterone and estrogen, and differences in the number of immune-related genes on the X chromosome [20]. The production of androgens in the male fetus begins within the first trimester at ten weeks of gestation, marking an early initiation of sex differentiation while also affecting the developing immune system [20].
There is a constant increase in the testosterone serum level in male newborns over the first three months after birth, with a decrease at 7–12 months of life, followed by a maintenance of low-level serum testosterone until the onset of puberty. In female newborns, there is a decrease in testosterone serum levels after birth. These sex differences are uniquely observed within the first year of life, as serum testosterone reaches equal levels in male and female children at pre-puberty, followed by a significant change with the onset of puberty [20]. Overall, estrogen stimulates the proliferation of B cells, while testosterone suppresses the latter [21]. Regarding T cell subpopulations, testosterone also suppresses early-stage lymphopoiesis. Passing several developmental steps, T cells abandon the expressing androgen receptors. Although female neutrophils and macrophages showed a better phagocyte activity [22], testosterone reduces the production of tumor necrosis factor (TNF) and expression of toll-like receptor 4 (TLR-4), and increases cytokine release. Therefore, autoimmune-mediated diseases are more frequently observed in women [20].
Alongside hormones, the X-chromosome also plays an important role in this context. Coding regions for genes involved in immune responses, such as toll-like receptors, cytokine receptors, and transcription factors can be found on the X-chromosome [23]. During embryogenesis, there is a random silencing of one X chromosome. At the same time, there is an escape out of this silencing process in 15% out of the immune-related genes; with 10% of these genes underlying the different levels of inactivation [24]. Thus, an overexpression of these immune-related genes is associated to X disomy. Genes associated to autoimmunity are also found on the X chromosomes, such as the expression of TLR-7, which has described in relation to lupus-associated autoimmunity [25].
A recent example for sex disparity and their associated different clinical courses and outcomes are infections with severe acute respiratory syndrome coronavirus 2. The underlying mechanism remains elusive, and the influence of estrogens and androgens, as well as androgen-sensitive genes coding for angiotensin-converting enzyme 2 (ACE2) and cell surface transmembrane protease serine 2 (TMPRSS2) are under discussion, as well as their sociocultural influences [26].
The cord blood reflects a unique period of early immune system development. Until now, there has been limited evidence regarding sex differences in the leucocytes in the cord blood. Our study aims to gain a deeper comprehension of the composition of the B and T cell subpopulations in the cord blood with respect to sex. In addition, we aimed to investigate whether there are sex-related differences within the lymphocyte subpopulations in the cord blood.

2. Results

2.1. B Cells

We analyzed the cord blood samples of 16 male newborns and 21 female newborns using flow cytometry. The mean of B1 cells was significantly higher in the cord blood of male neonates than in the cord blood of female neonates (male 3.7% ± 2.9 vs. female 1.8% ± 1.5, p = 0.023, Figure 1, Table 1). B1 cells are marked as CD20+ CD27+ CD43+ and are given as a percentage of the number of total CD20+ cells. Marginal zone memory B cells, marked as CD19+ CD27+ IgD+ IgM+, and given as a percentage of total CD19+ cells, were also found to be significantly higher in male cord blood (male 1.7% ± 2.1 vs. female 0.8% ± 1.2, p = 0.01, Figure 2, Table 1). With the exception of the naïve B cells and transitional B cells, the B cell count in all other subsets (innate B cells, class-switched memory B cells, late memory B cells, plasmablasts, transitional B cells, and B2 cells) was found to be higher in the cord blood of male newborns (Table 1).

2.2. T Cells

We analyzed T cell subpopulations in two panels. In T cell panel 1, we analyzed 16 male and 21 female newborns, and in T cell panel 2 we analyzed 11 male and 16 female newborns with flow cytometry, respectively.
Cytotoxic T cells, naïve effector Th cells, naïve effector cytotoxic T cells, and naïve thymus-negative Th cells all demonstrated an increasing trend in the cord blood of male newborns. Naïve thymus-negative Th cells were significantly more abundant in male cord blood (male 24.4% ± 9.8 vs. female 15.9 ± 5.7, p = 0.05, Figure 3, Table 2). In cord blood, 12 other T cell subpopulations (T helper cells, T helper cells with αβ-TCR, activated cytotoxic T helper cells with αβ-TCR, memory effector T helper cells, naïve central T helper cells, naïve central T helper cells, memory effector cytotoxic T cells, memory central cytotoxic T cells, naïve central cytotoxic T cells, and naïve thymus-positive T helper cells) showed a non-significant higher count in the cord blood of female newborns than in male newborns (Table 2). The remaining subpopulations (T helper cells 1, naïve T helper cells 1, memory T helper cells 1, T helper cells 2, naïve T helper cells 2, memory T helper cells 2, and regulatory T cells) showed similar cell counts in both sexes.

3. Discussion

In our study, we found significant differences in the B and T cell populations (Table 3) between male and female newborns. We were able to generate reference values for the means of nine B cell subpopulations and twenty-one T cell subpopulations, respectively.
Although sex-related immunity differences have been observed in children and adults, very little is known about sex differences at birth. Research data about the latter are sparse, and pathophysiologic pathways and their mechanisms remain elusive. Sex differences in immune responses are traced back to two main factors: the influence of sex hormones, such as testosterone and estrogen, and differences in the number of immune-related genes on the X chromosome [20].
The production of androgens in the male fetus begins within the first trimester at ten weeks of gestation, marking an early initiation of sex differentiation, and also affecting the developing immune system [20]. In vitro, estradiol increases the accumulation of B cells, but in non-toxic doses, it does not affect the proliferation response. Moreover, it exhibits the same effect on the lymphocytes of both males and females. Non-toxic concentrations of testosterone do not influence the maturation of B cells in vitro [1]. Sex hormones also influence the T cell subpopulations. For instance, testosterone suppresses lymphopoiesis only during its early stages. After further development, T cells do not express androgen receptors. However, estrogen receptors can be expressed at any stage of T cell development: low doses of estrogen increase CD4+ cells, while high doses of estrogen reduce CD4 and CD8 cell counts [27]. In our analysis, the means of four out of fourteen T cell subpopulations (cytotoxic T cells, naïve effector Th cells, naïve effector cytotoxic T cells, and naïve thymus-negative Th cells) showed a trend to be higher in the cord blood of male newborns. The remaining T cell subpopulations were expected to be higher in the female newborns.
Here, the umbilical cord blood allows a special insight into the intrauterine lymphocyte profiles, as it represents an interphase between the pre–and postnatal physiology. In our analysis, B cell populations were higher in the male newborns compared to the female newborns, except for the naïve B cell and transitional B cell populations. These results are contrary to the relation of B cells in adult blood, with higher B cell counts observed in females than in males [28]. Possible reasons include changes in sex hormone levels in utero compared to levels after birth: estrogen stimulates the proliferation of B cells, while testosterone suppresses the latter [21]. After birth, there is an increase in testosterone levels in male newborns during the first three months, followed by a decrease to much lower levels before reaching pre-puberty low levels (at around 7–12 months of age). Females, on the other hand, experience a decrease in testosterone immediately after birth. Beyond the first year of life until adolescence, there are no sex-specific differences impacting the testosterone levels [20,29]. This fact may lead to the assumption that sex hormones are less relevant during this period of life. In this time, partially unknown factors, apart from sex hormones, might play an important role in the development of the immune system.
The influence of immune-related genes on the X chromosome, leading to sex differences in the development of immune-associated diseases, begins early in life [20].
X disomy leads to a higher genetic variety observed among these immune-related genes. Toll-like receptor 7/8 is able to detect viral single-stranded RNA (ss-RNA) and induce protective cytokine responses, in particular IFN responses. Although male and female innate immune cells do not differ significantly in terms of their overall TLR 7/8 expression, a humanized mouse model showed a positive influence of TLR7 ligation on the plasmacytoid dendritic cells and its interferon-α (IFN-α) and TNF responses [30]. Micro-RNAs (mi-RNA) as non-coding RNAs are associated with inflammatory diseases. The loci of mi-RNA have been found of higher amounts on the X chromosomes compared to the Y-chromosomes and autosomes [30]. X-linked miR223 seems to play a crucial role: studies have suggested that miR223-negative mice showed more inflammatory symptoms compared to non-deficient mice following Candida albicans infection, wherein miR223 is supposed to affect granulocyte generation and maturation negatively [31,32].
Men are more prone to infection-induced inflammation [33], like respiratory tract infections (RTI). Being more susceptible to RTI than women, severe courses of RTI infections are more often seen in males. This might be due to the innate immune response and its sex differences. A possible explanation could be the observed imbalance of TLR-2 and TLR-4: there is a higher expression of TLR-4 in the macrophages of male mice following endotoxic shock, leading to the extensive production of pro-inflammatory cytokines [34]. A protective factor seems to be the expression of TLR-2, which was found to be higher in female mice augmenting resistance against viral infections (especially coxsackie virus) [35]. Estrogen, on the other hand, suppresses lung inflammation in animal models [35]. The X-chromosome, and its linked immune-related genes, such as TLR 7/8-encoding genes, might also be responsible for these sex differences in infection-induced inflammation [36].
Former research has revealed a postnatal increase in CD19+ B cells and CD3+ T cells, until the age of 2 years, followed by a gradual decrease until adulthood. While CD3+ CD4+ T lymphocytes comply with this trend, the subpopulation of CD3+ CD8+ T lymphocytes remains stable for the first two years of life followed by a constant decrease until reaching levels similar to adults [37]. Overall, no sex differences were considered in the aforementioned studies. Various influences on the lymphocyte populations within this period, such as X chromosomal genes, must be considered when analyzing data on the developing immune system. There is less evidence available in the literature on sex-related changes in these lymphocyte subpopulations, and more research is necessary to illuminate all factors leading to the observed changes.
Even though there is a lot of data available on the CD4+ and CD8+ T cell sex differences in general, there is still a lack of evidence regarding sex differences in smaller lymphocyte subpopulations. We provided reference values for the means of 21 different T cell subpopulations. There is a need for further studies to gain more data about the sex-related differences in these subgroups in order to identify the sex-related risk factors for specific diseases.
Regardless of the sparse data on sex differences in the immunity (or immune development) of neonates, the published research so far indicates that male newborns are more prone to develop a robust innate immunity, characterized by higher counts of natural killer (NK) cells, monocytes, and basophils. Male newborns additionally show a better pro inflammatory response compared to females [23]. However, females do have higher CD4+ T cells and CD4/CD8 ratios, lower CD8+ T cells, and lower Treg cell frequencies [23]. The numbers of B cells, IgG, and IgM are similar in both sexes, whilst male newborns show a higher IgA and IgE count than females [23]. Our data suggest that there are no changes in the total population of B or T cells, but there are changes in their subpopulations. The subpopulations of the B and T lymphocytes are very inhomogeneous groups that exert different influences and react differently to certain stimulations. More studies are needed to identify the factors leading to changes in these lymphocyte subpopulations [23].
Sex differences in in the immune response can be observed throughout childhood. Males exhibit higher levels of inflammation and NK cells, while CD4/CD8 ratios, CD8+ cells, CD4+ cells, and B cell numbers are similar in both sexes [23,33]. The onset of puberty marks a shift in the sex-specific immune response, potentially influenced by sex steroids. In adult females, higher inflammation, CD4/CD8 ratios, and CD4+ cell counts are observed, whereas adult males display higher counts of CD8+ cells, B cells, and immunoglobulins, with Treg cells also being higher in males [23]. After menopause, males exhibit a higher pro-inflammatory response, while females show an increased T cell activation. Other sex differences, such as the CD4+ CD8+ cell count and the CD4/CD8 ratio, remain equally distributed [23].
We found a significant difference in the MZ B cells (p = 0.025). Even though they only count for 5% of all B cells, they play an important role in the early immune response. MZ B cells are located at a strategic interface between blood and the lymph nodes, meaning they are able to react promptly with the antibody response and bacterial pathogens [1]. They close the gap between the early immune response and the late adaptive antibody reactions of follicular B cells [15]. This finding contradicts previously published data, as females of all ages have been found to exhibit greater total B cell numbers. The latter could be an example of changes in the composition of lymphocyte populations after birth, which may contribute to the sex-related differences observed in diseases during the neonatal period and later in life.
B1 cells, defined as CD20+ CD27+ CD43+, also exhibited a significant difference (p = 0.01). B1 cells constitute the main portion of B lymphocytes in newborns, but decrease to approximately 10% by adulthood [13].This illustrates that B1 cells are a dynamic component of the immune system, undergoing continuous changes during the development of a “mature” immune response. B1 cells play a crucial role in the innate immune system. However, certain underlying pathomechanisms remain elusive [38]. Establishing a consistent definition of immune markers is essential to ensure comparability among the studies investigating the B1 cell (sub)-populations. A major finding of our study was a higher count of B1 cells in male newborns. B1 cells are associated with the pathogenesis of asthma and allergies, particularly in relation to the production of IgE antibodies, which promote the regulation of the inflammatory processes [39,40], and the development of autoimmune diseases, predominantly affecting women [41]. Our findings suggest changes in the composition of B1 cells after birth, potentially due to environmental influences, antigen exposure, or the development of the adaptive immune response.
Thymus-negative T cells were found to be significantly higher in male newborns (p = 0.005). Innate T cells migrate from the bone marrow to the thymus, where they undergo both positive and negative selection. During the positive selection process, Th cells that are able to bind to the MHC complexes receive a positive growing signal and enter the cell cycle. This positive selection takes place in the postnatal thymus, indicating that the maturation of Th cells is still an ongoing process by the time of birth [1]. Thymus-negative T cells are innate cells that have not completed positive and negative selection. After negative selection, mature T cells leaving the thymus tissue usually carry the CD31 marker. Negative selection plays a crucial role in the prevention of the development of autoimmune reactive cells. There are tissue-specific antigens expressed in the thymus. Autoimmune regulator genes (AIRE) control the expression of these antigens. Mutations in this gene can result in an autoimmune disease known as autoimmune polyglandular syndrome 1 (APS-1) [16]. Therefore, changes in the thymus-negative T cell count could be involved in development of autoimmune diseases, including APS-1. There are studies hinting at a correlation between a failure in negative thymus selection and rheumatoid arthritis [42]. Alterations in thymus-negative cell counts could potentially induce dysregulation in the immune system, resulting in either a reduced or incorrect pathogen detection.
This research can potentially lead to improvements in prenatal diagnostics by introducing new early detection screenings during pregnancy, including tests capturing specific parameters related to sex-specific differences in lymphocyte subpopulations and other immunological features. A better understanding of early childhood immunity could also result in adjustments towards sex-specific vaccination schedules. In the clinical context, a sex-based medication regime is possible based on the different immunological mechanisms. Furthermore, examining the prenatal phenotype of lymphocytes could build a basis for the development of individually tailored therapeutic approaches.
There are several limitations in our study. The main limitation is the very small sample size. The latter may contribute to that fact that small differences might not be detected within our cohort. In addition, small cohorts may not be representative for the overall population, thereby limiting the generalizability of our findings. Overall, small cohorts restrict the range of statistical analyses that can be performed due to the limited number of cases. Nevertheless, pre- and perinatal variables regarding the recruited neonates and their mothers have been taken into account to avoid confounders. Only mothers without autoimmune diseases and without any infections or antibiotic intake within the last 2 weeks before birth were included. Furthermore, only infants delivered by caesarean section were included in the study to enhance the comparability. All included children were term-born (up to 37 + 0 weeks of gestation).
Further studies are necessary to validate these findings. Follow-up examinations to investigate the relationship between the gender-specific differences in the umbilical cord blood and the occurrence of diseases are feasible. To detect changes in immunological development, follow-up blood samples, optimally during routine examinations, are necessary. Additional investigations with an extended cohort size are needed to verify these results. Gene expression analysis or epigenetic studies must be considered in future research to investigate the underlying molecular mechanisms.
In conclusion, our study identified significant differences in cord blood lymphocytes related to male and female neonates. Sex-related differences undergo changes throughout the development towards a mature immune response. We provide reference values for nine B cell and 21 T cell subpopulations in the cord blood, suggesting valuable data on the influence of sex on the developing immune system. Further investigations are elusive to enlighten the understanding of early immune development and its sex-related differences in neonates, infants, children, and young adults, along with their clinical consequences.

4. Materials and Methods

4.1. Patient Samples

We collected blood samples from the umbilical cord blood of term neonates (range 37–40 weeks gestation, n = 37) without any infectious, immunologic, or chronical disease or antibiotic treatment in the previous two weeks, before planned caesarean sections. The Ethics Committee of Saarland approved the study protocol (198/20, 6 August 2020). The written informed consent of all the parents was obtained.

4.2. Cell Isolation, Storage, and Counting

Cell Isolation and Storage

Cord blood was collected into S-Monovette® K3 ethylene diamine tetraacetic acid (EDTA, Sarstedt, Nümbrecht, Germany). Cord blood mononuclear cells (CBMCs) were prepared from the whole blood through density gradient centrifugation using the Lymphocyte Separation Medium 1.077, FicoLite-H (Linaris biological products, Dossenheim, Germany). Whole blood was diluted 1:1 with D-PBS followed by layering the mixture 1.5:1 on FicoLite-H. Samples were centrifuged at 400× g for 30 min. Interphase was considered as CBMCs and were separated. Cells were washed twice using Dulbecco’s phosphate-buffered saline (D-PBS, Sigma Aldrich, Steinheim, Germany) and were centrifuged at 400× g for 10 min. Subsequently, CBMCs were resuspended in fetal bovine serum (FBS, Thermo Fisher Scientific, Waltham, MA, USA) + 10% dimethylsufoxid (DSMO, Sigma Aldrich, Steinheim, Germany) and were placed in a CellCamper® for cryopreservation at −80 °C.

4.3. Flow Cytometry

On the day of the experiment, the cryopreserved cells were gradually thawed by first acclimating the frozen vial on ice and then thawing the cell pellet in a water bath at room temperature. Cell pellets were then washed twice using D-PBS and centrifuged at 400× g for 10 min) prior to the quantification of the viable and dead cells. For this purpose, a portion of the cell suspension was stained with acridine orange and propidium iodide (AO/PI) and was quantitatively analyzed using the LUNA-FL™ Automated Fluorescence Cell Counter (Logos Biosystems, Dongan-gu Anyang-si, Gyeonggi-do, Republic of Korea) according to the manufacturer’s instructions. Following this, BD Horizon Fixable Viability Stain 780 (BD Biosciences, Heidelberg, Germany) was used for staining the dead cells according to the manufacturer’s instructions. Cells were washed using BD CellWASH™ (BD Biosciences, Heidelberg, Germany) and were centrifuged at 500× g for 10 min. Fluorochrome-conjugated antibodies are listed in Table 4. Cell pellets were resuspended in a panel-specific antibody mix containing BD Horizon™ Brilliant Stain Buffer (BD Biosciences, Heidelberg, Germany) and BD Pharmingen™ Stain buffer BSA. Samples were incubated protected from light at room temperature for 30 min. The remaining erythrocytes were lyzed with BD FACS™ Lysing Solution (BD Biosciences, Heidelberg, Germany) according to the manufacturer’s protocol. The cell suspension was diluted by BD CellWASH™ and was centrifuged at 500× g for 10 min. Cell pellets were resuspended in D-PBS and were then analyzed on a 3-laser, 12-color FACS Celesta flow cytometer (Becton, Dickinson and Company, Heidelberg, Germany).
Flow cytometer performance, stability, fluorescence calibrations, and data reproducibility were sustained and checked daily using the Cytometer Setup and Tracking Module (CS&T, BD Biosciences, Heidelberg, Germany). Application settings were applied for each acquisition and Sphero™ Rainbow Calibration Particles (8 Peaks, BD Biosciences, Heidelberg, Germany) were used to validate the reproducibility of the data over time. Compensation settings were calculated using BD™ CompBeads (BD Biosciences, Heidelberg, Germany). Comparison of the stained sample with an unstained sample, a sample subjected to all procedures except antibody staining, and the isotype control to specify the non-specific binding of the antibodies, constituted the basis for the positive staining and gating strategy. Cell aggregates were removed from the analysis (FSC-A/FSC-H) and dead cells were excluded from the analysis by staining with BD Horizon Fixable Viability Stain 780. Lymphocyte classification based on morphological parameters (FSC-A/SSC-A) was confirmed at the end.
Data were acquired using FACSDiva (BD Biosciences, Heidelberg, Germany) and were analyzed using FlowJo v10 (BD Biosciences). The gates were preset and the measurements were performed blinded for sample identity (Figure 4, Figure 5 and Figure 6).

4.4. Statistical Analysis

Statistical analysis was performed using SPSS 28.0.0. (IBM, Chicago, IL, USA). Quantitative data was examined for normal distribution using the Shapiro–Wilk test. The majority of variables did not follow a normal distribution. Thus, we used the exact version of the Mann–Whitney U test for all comparisons between the male and female newborns. The p-values were two-sided and subjected to a significance level of 0.05. Due to the explorative nature of the investigation, we did not account for multiple statistical testing, and therefore reported raw, unadjusted p-values. Descriptive statistics were reported as mean with standard deviation.

Author Contributions

M.B.: conception and design, coordination of sample collection, data analysis and interpretation, manuscript writing, final approval of manuscript. C.S.: collection and assembly of data, manuscript writing, final approval of manuscript. S.T.: coordination of sample collection, manuscript writing, final approval of manuscript. B.H.H., E.-F.S.: manuscript writing, final approval of manuscript. R.W., M.C.H.: collection and assembly of data, data analysis, manuscript writing, final approval of manuscript. E.K.: collection and assembly of data, manuscript writing. G.W.: data analysis and interpretation, manuscript writing, final approval of manuscript. N.N.-T.: manuscript writing, final approval of manuscript. M.Z.: conception and design, data analysis and interpretation, financial support, manuscript writing, final approval of manuscript. S.G.-F.: conception and design, coordination of sample collection, data analysis and interpretation, manuscript writing, final approval of manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

Funded by a grant from the HOMFOR Foundation of Saarland University Medical School, by the Else-Kröner-Fresenius Stiftung, by the Staatskanzlei Saarbrücken, by the Centre of Digital Neurotechnologies Saar, by the Werner-Zeh-Stiftung, and by the BMBF (PRIMAL Clinical Study FKZ: 01GL1746D).

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Ethics Committee of Saarland University (198/20, 6 August 2020).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

We thank Ellen Maurer for her excellent technical help.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. LeBien, T.W.; Tedder, T.F. B lymphocytes: How they develop and function. Blood 2008, 112, 1570–1580. [Google Scholar] [CrossRef] [Green Version]
  2. Rackaityte, E.; Halkias, J. Mechanisms of Fetal T Cell Tolerance and Immune Regulation. Front. Immunol. 2020, 11, 588. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. Prescott, S.; Saffery, R. The role of epigenetic dysregulation in the epidemic of allergic disease. Clin. Epigenet. 2011, 2, 223–232. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Kogan, V.; Millstein, J.; London, S.J.; Ober, C.; White, S.R.; Naureckas, E.T.; Gauderman, W.J.; Jackson, D.J.; Barraza-Villarreal, A.; Romieu, I.; et al. Genetic-Epigenetic Interactions in Asthma Revealed by a Genome-Wide Gene-Centric Search. Hum. Hered. 2018, 83, 130–152. [Google Scholar] [CrossRef]
  5. Wilson, A.G. Epigenetic regulation of gene expression in the inflammatory response and relevance to common diseases. J. Periodontol. 2008, 79, 1514–1519. [Google Scholar] [CrossRef] [Green Version]
  6. Henneke, P.; Kierdorf, K.; Hall, L.J.; Sperandio, M.; Hornef, M. Perinatal development of innate immune topology. eLife 2021, 10, e67793. [Google Scholar] [CrossRef]
  7. Cerutti, A.; Cols, M.; Puga, I. Marginal zone B cells: Virtues of innate-like antibody-producing lymphocytes. Nat. Rev. Immunol. 2013, 13, 118–132. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Maródi, L. Neonatal Innate Immunity to Infectious Agents. Infect. Immun. 2006, 74, 1999–2006. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Arrieta, M.-C.; Stiemsma, L.T.; Dimitriu, P.A.; Thorson, L.; Russell, S.; Yurist-Doutsch, S.; Kuzeljevic, B.; Gold, M.J.; Britton, H.M.; Lefebvre, D.L.; et al. Early infancy microbial and metabolic alterations affect risk of childhood asthma. Sci. Transl. Med. 2015, 7, 307ra152. [Google Scholar] [CrossRef]
  10. Kumar, S.K.M.; Bhat, B.V. Distinct mechanisms of the newborn innate immunity. Immunol. Lett. 2016, 173, 42–54. [Google Scholar] [CrossRef]
  11. Basha, S.; Surendran, N.; Pichichero, M. Immune Responses in Neonates. Expert Rev. Clin. Immunol. 2014, 10, 1171–1184. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Simon, A.K.; Hollander, G.A.; McMichael, A. Evolution of the immune system in humans from infancy to old age. Proc. Biol. Sci. 2015, 282, 20143085. [Google Scholar] [CrossRef] [PubMed]
  13. Griffin, D.O.; Holodick, N.E.; Rothstein, T.L. Human B1 cells in umbilical cord and adult peripheral blood express the novel phenotype CD20+ CD27+ CD43+ CD70−. J. Exp. Med. 2011, 208, 67–80. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Prabhu, S.B.; Rathore, D.K.; Nair, D.; Chaudhary, A.; Raza, S.; Kanodia, P.; Sopory, S.; George, A.; Rath, S.; Bal, V.; et al. Comparison of Human Neonatal and Adult Blood Leukocyte Subset Composition Phenotypes. PLoS ONE 2016, 11, e0162242. [Google Scholar] [CrossRef] [Green Version]
  15. Lopes-Carvalho, T.; Kearney, J.F. Development and selection of marginal zone B cells. Immunol. Rev. 2004, 197, 192–205. [Google Scholar] [CrossRef] [PubMed]
  16. Murphy, K.; Weaver, C. Die Entwicklung der B- und T-Lymphocyten. Janeway Immunol. 2018, 9, 377–440. [Google Scholar] [CrossRef]
  17. Lind, E.F.; Prockop, S.E.; Porritt, H.E.; Petrie, H.T. Mapping Precursor Movement through the Postnatal Thymus Reveals Specific Microenvironments Supporting Defined Stages of Early Lymphoid Development. J. Exp. Med. 2001, 194, 127–134. [Google Scholar] [CrossRef] [Green Version]
  18. Cooper, G.S.; Stroehla, B.C. The epidemiology of autoimmune diseases. Autoimmun. Rev. 2003, 2, 119–125. [Google Scholar] [CrossRef]
  19. Jacobson, D.L.; Gange, S.J.; Rose, N.R.; Graham, N.M. Epidemiology and estimated population burden of selected autoimmune diseases in the United States. Clin. Immunol. Immunopathol. 1997, 84, 223–243. [Google Scholar] [CrossRef] [Green Version]
  20. Libert, C.; Dejager, L.; Pinheiro, I. The X chromosome in immune functions: When a chromosome makes the difference. Nat. Rev. Immunol. 2010, 10, 594–604. [Google Scholar] [CrossRef]
  21. Bereshchenko, O.; Bruscoli, S.; Riccardi, C. Glucocorticoids, Sex Hormones, and Immunity. Front. Immunol. 2018, 9, 1332. [Google Scholar] [CrossRef] [Green Version]
  22. Spitzer, J.A. Gender differences in some host defense mechanisms. Lupus 1999, 8, 380–383. [Google Scholar] [CrossRef] [PubMed]
  23. Klein, S.L.; Flanagan, K.L. Sex differences in immune responses. Nat. Rev. Immunol. 2016, 16, 626–638. [Google Scholar] [CrossRef] [PubMed]
  24. Carrel, L.; Willard, H.F. X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature 2005, 434, 400–404. [Google Scholar] [CrossRef]
  25. Lyn-Cook, B.D.; Xie, C.; Oates, J.; Treadwell, E.; Word, B.; Hammons, G.; Wiley, K. Increased expression of Toll-like receptors (TLRs) 7 and 9 and other cytokines in systemic lupus erythematosus (SLE) patients: Ethnic differences and potential new targets for therapeutic drugs. Mol. Immunol. 2014, 61, 38–43. [Google Scholar] [CrossRef] [PubMed]
  26. Lott, N.; Gebhard, C.E.; Bengs, S.; Haider, A.; Kuster, G.M.; Regitz-Zagrosek, V.; Gebhard, C. Sex hormones in SARS-CoV-2 susceptibility: Key players or confounders? Nat. Rev. Endocrinol. 2023, 19, 217–231. [Google Scholar] [CrossRef]
  27. Lai, J.-J.; Lai, K.-P.; Zeng, W.; Chuang, K.-H.; Altuwaijri, S.; Chang, C. Androgen Receptor Influences on Body Defense System via Modulation of Innate and Adaptive Immune Systems: Lessons from Conditional AR Knockout Mice. Am. J. Pathol. 2012, 181, 1504–1512. [Google Scholar] [CrossRef] [Green Version]
  28. Abdullah, M.; Chai, P.-S.; Chong, M.-Y.; Tohit, E.R.M.; Ramasamy, R.; Pei, C.P.; Vidyadaran, S. Gender effect on in vitro lymphocyte subset levels of healthy individuals. Cell. Immunol. 2012, 272, 214–219. [Google Scholar] [CrossRef]
  29. Forest, M.G.; Cathiard, A.M.; Bertrand, J.A. Evidence of testicular activity in early infancy. J. Clin. Endocrinol. Metab. 1973, 37, 148–151. [Google Scholar] [CrossRef]
  30. Laffont, S.; Rouquié, N.; Azar, P.; Seillet, C.; Plumas, J.; Aspord, C.; Guéry, J.-C. X-Chromosome complement and estrogen receptor signaling independently contribute to the enhanced TLR7-mediated IFN-α production of plasmacytoid dendritic cells from women. J. Immunol. 2014, 193, 5444–5452. [Google Scholar] [CrossRef] [Green Version]
  31. Johnnidis, J.B.; Harris, M.H.; Wheeler, R.T.; Stehling-Sun, S.; Lam, M.H.; Kirak, O.; Brummelkamp, T.R.; Fleming, M.D.; Camargo, F.D. Regulation of progenitor cell proliferation and granulocyte function by microRNA-223. Nature 2008, 451, 1125–1129. [Google Scholar] [CrossRef] [PubMed]
  32. Haneklaus, M.; Gerlic, M.; O’Neill, L.A.J.; Masters, S.L. miR-223: Infection, inflammation and cancer. J. Intern. Med. 2013, 274, 215–226. [Google Scholar] [CrossRef] [PubMed]
  33. Chamekh, M.; Deny, M.; Romano, M.; Lefèvre, N.; Corazza, F.; Duchateau, J.; Casimir, G. Differential Susceptibility to Infectious Respiratory Diseases between Males and Females Linked to Sex-Specific Innate Immune Inflammatory Response. Front. Immunol. 2017, 8, 1806. [Google Scholar] [CrossRef]
  34. Lamason, R.; Zhao, P.; Rawat, R.; Davis, A.; Hall, J.C.; Chae, J.J.; Agarwal, R.; Cohen, P.; Rosen, A.; Hoffman, E.P.; et al. Sexual dimorphism in immune response genes as a function of puberty. BMC Immunol. 2006, 7, 2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Scotland, R.S.; Stables, M.J.; Madalli, S.; Watson, P.; Gilroy, D.W. Sex differences in resident immune cell phenotype underlie more efficient acute inflammatory responses in female mice. Blood 2011, 118, 5918–5927. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Kondo, Y.; Miyazato, A.; Okamoto, K.; Tanaka, H. Impact of Sex Differences on Mortality in Patients with Sepsis after Trauma: A Nationwide Cohort Study. Front. Immunol. 2021, 12, 678156. [Google Scholar] [CrossRef]
  37. Comans-Bitter, W.M.; de Groot, R.; van den Beemd, R.; Neijens, H.J.; Hop, W.C.; Groeneveld, K.; Hooijkaas, H.; van Dongen, J.J. Immunophenotyping of blood lymphocytes in childhood. Reference values for lymphocyte subpopulations. J. Pediatr. 1997, 130, 388–393. [Google Scholar] [CrossRef] [Green Version]
  38. Baumgarth, N. The double life of a B-1 cell: Self-reactivity selects for protective effector functions. Nat. Rev. Immunol. 2011, 11, 34–46. [Google Scholar] [CrossRef]
  39. Rothstein, T.L.; Griffin, D.O.; Holodick, N.E.; Quach, T.D.; Kaku, H. Human B-1 cells take the stage. Ann. N. Y. Acad. Sci. 2013, 1285, 97–114. [Google Scholar] [CrossRef] [Green Version]
  40. Kawikova, I.; Paliwal, V.; Szczepanik, M.; Itakura, A.; Fukui, M.; Campos, R.A.; Geba, G.P.; Homer, R.J.; Iliopoulou, B.P.; Pober, J.S.; et al. Airway hyper-reactivity mediated by B-1 cell immunoglobulin M antibody generating complement C5a at 1 day post-immunization in a murine hapten model of non-atopic asthma. Immunology 2004, 113, 234–245. [Google Scholar] [CrossRef]
  41. Deng, J.; Wang, X.; Chen, Q.; Sun, X.; Xiao, F.; Ko, K.-H.; Zhang, M.; Lu, L. B1a cells play a pathogenic role in the development of autoimmune arthritis. Oncotarget 2016, 7, 19299–19311. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Fournier, C. Where Do T Cells Stand in Rheumatoid Arthritis? Jt. Bone Spine 2005, 72, 527–532. [Google Scholar] [CrossRef] [PubMed]
Ijms 24 11511 g001 550
Figure 1. B1 lymphocytes (CD20+ CD27+ CD43+) percentage of CD20+ [%] were significantly higher in male (n = 16) than in female (n = 21) newborns, given with the median (male = 2.7, female = 1.6), minimum (male = 0.3, female = 0.2), and maximum values (male = 10, female = 5.8); mean ± standard deviation [%] (male = 3.7 ± 2.9, female = 1.8 ± 1.2). Outliers are marked with dots and (*).
Figure 1. B1 lymphocytes (CD20+ CD27+ CD43+) percentage of CD20+ [%] were significantly higher in male (n = 16) than in female (n = 21) newborns, given with the median (male = 2.7, female = 1.6), minimum (male = 0.3, female = 0.2), and maximum values (male = 10, female = 5.8); mean ± standard deviation [%] (male = 3.7 ± 2.9, female = 1.8 ± 1.2). Outliers are marked with dots and (*).
Ijms 24 11511 g001
Ijms 24 11511 g002 550
Figure 2. Marginal zone B lymphocytes (CD19+ CD27+ IgD+ IgM+). The percentage of CD19+ cells [%], were higher in male (n = 16) than in female (n = 21) newborns, given with the median (male = 0.8, female = 0.4), minimum (male = 0.1, female = 0.1), and maximum values (male = 7, female = 4.3); mean ± standard deviation [%] (male = 1.7 ± 2.1, female = 0.8 ± 1.2).
Figure 2. Marginal zone B lymphocytes (CD19+ CD27+ IgD+ IgM+). The percentage of CD19+ cells [%], were higher in male (n = 16) than in female (n = 21) newborns, given with the median (male = 0.8, female = 0.4), minimum (male = 0.1, female = 0.1), and maximum values (male = 7, female = 4.3); mean ± standard deviation [%] (male = 1.7 ± 2.1, female = 0.8 ± 1.2).
Ijms 24 11511 g002
Ijms 24 11511 g003 550
Figure 3. Thymus-negative T lymphocyte (CD3+ CD4+ CD31− CD45RO− ) percentages of CD3+ CD4+ [%] were significantly higher in male (n = 16) than in female (n = 21) newborns (see Figure 1), given with the median (male = 21, female = 16.2), minimum (male 9.4, female 4.2), and maximum values (male 42.3, female = 27.1); mean ± standard deviation [%] (male = 24.4 ± 9.8, female = 15.9 ± 5.7). Outliers are marked with dots.
Figure 3. Thymus-negative T lymphocyte (CD3+ CD4+ CD31− CD45RO− ) percentages of CD3+ CD4+ [%] were significantly higher in male (n = 16) than in female (n = 21) newborns (see Figure 1), given with the median (male = 21, female = 16.2), minimum (male 9.4, female 4.2), and maximum values (male 42.3, female = 27.1); mean ± standard deviation [%] (male = 24.4 ± 9.8, female = 15.9 ± 5.7). Outliers are marked with dots.
Ijms 24 11511 g003
Ijms 24 11511 g004 550
Figure 4. Gating strategy for B cell subpopulations of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD19+ and CD20+ cells was determined. The CD19+ fraction was divided into CD27+ and CD27− B cells. CD27+ cells were subdivided into marginal zone memory B cells (IgD+ IgM+), class-switched memory B cells (IgD− IgM−), late memory B cells (CD38+ IgM+) and plasmablasts (CD38++ IgM−). CD27− cells were subdivided into innate B cells (IgD− IgM−), naïve B cells (IgD+ IgM+), and transitoneal B cells (CD20+ CD38+). CD20+ cells were subdivided into B1 cells (CD27+ CD43+) and B2 cells (CD27+ CD43−).
Figure 4. Gating strategy for B cell subpopulations of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD19+ and CD20+ cells was determined. The CD19+ fraction was divided into CD27+ and CD27− B cells. CD27+ cells were subdivided into marginal zone memory B cells (IgD+ IgM+), class-switched memory B cells (IgD− IgM−), late memory B cells (CD38+ IgM+) and plasmablasts (CD38++ IgM−). CD27− cells were subdivided into innate B cells (IgD− IgM−), naïve B cells (IgD+ IgM+), and transitoneal B cells (CD20+ CD38+). CD20+ cells were subdivided into B1 cells (CD27+ CD43+) and B2 cells (CD27+ CD43−).
Ijms 24 11511 g004
Ijms 24 11511 g005 550
Figure 5. Gating strategy for T cell subpopulations (Panel 1) of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD3+ cells was determined. The CD3+ fraction was divided into CD4+ T helper cells and CD8+ cytotoxic T cells. Both cell fractions were subdivided into naïve central (CD62L+ CD45RO−), naïve effector (CD62L− CD45RO−), memory effector (CD62L− CD45RO+), and memory central (CD62L+ CD45RO+) T cells subpopulations, along with T cells with TCRαβ, and activated T cells with TCRαβ (CD69+) were all identified. CD4+ Th cells were further subdivided into naïve thymus-negative (CD45RO− CD31−) and positive (CD45RO− CD31+) Th cells.
Figure 5. Gating strategy for T cell subpopulations (Panel 1) of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD3+ cells was determined. The CD3+ fraction was divided into CD4+ T helper cells and CD8+ cytotoxic T cells. Both cell fractions were subdivided into naïve central (CD62L+ CD45RO−), naïve effector (CD62L− CD45RO−), memory effector (CD62L− CD45RO+), and memory central (CD62L+ CD45RO+) T cells subpopulations, along with T cells with TCRαβ, and activated T cells with TCRαβ (CD69+) were all identified. CD4+ Th cells were further subdivided into naïve thymus-negative (CD45RO− CD31−) and positive (CD45RO− CD31+) Th cells.
Ijms 24 11511 g005
Ijms 24 11511 g006 550
Figure 6. Gating strategy of T cell subpopulations (Panel 2) of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD3+ cells was determined. CD4+ T helper cells were identified. Th1 cells (CD183+ CD196+) and Th2 cells (CD194+ CD294+), and their subpopulations naïve (CD45RO−) and memory (CD45RO+) were determined from the Th cell fraction. Regulatory Th cells were identified as CD25+ CD127−.
Figure 6. Gating strategy of T cell subpopulations (Panel 2) of a representative CBMC sample. Analysis was performed in FlowJo (BD Biosciences). The gating strategy was based on morphological parameters (FSC-H/FSC-A). FVS 780-negative cells were considered as viable cells. From the viable cells, the number of CD3+ cells was determined. CD4+ T helper cells were identified. Th1 cells (CD183+ CD196+) and Th2 cells (CD194+ CD294+), and their subpopulations naïve (CD45RO−) and memory (CD45RO+) were determined from the Th cell fraction. Regulatory Th cells were identified as CD25+ CD127−.
Ijms 24 11511 g006
Table
Table 1. Relative amounts of B lymphocyte subpopulations with mean and standard deviation [%]. Group differences were assessed using the Mann–Whitney U test. Test groups were divided into male (n = 16) and female (n = 21) newborns.
Table 1. Relative amounts of B lymphocyte subpopulations with mean and standard deviation [%]. Group differences were assessed using the Mann–Whitney U test. Test groups were divided into male (n = 16) and female (n = 21) newborns.
SexMean ± Standard Deviation [%]p-Value
Innate B cellsMale6.6 ± 4.00.8
(percentage of CD19+ cells)Female6.2 ± 3.7
Naïve B cells Male72.0 ± 11.70.53
(percentage of CD19+ cells)Female75.3 ± 8.3
Marginal zone memory B cells Male1.7 ± 2.10.01
(percentage of CD19+ cells)Female0.8 ± 1.2
Class-switched memory B cellsMale5.7 ± 4.10.84
(percentage of CD19 + cells)Female5.3 ± 2.6
Late memory B cellsMale3.2 ± 2.70.073
(percentage of CD19+ cells)Female1.7 ± 1.4
Plasmablasts Male5.5 ± 4.00.84
(percentage of CD19+ cells)Female5.2 ± 2.6
Transitonal B cells Male82.7 ± 11.00.89
(percentage of CD19+ cells)Female85.4 ± 6.7
B1 cells Male3.7 ± 2.90.023
(percentage of CD20+ cells)Female1.8 ± 1.5
B2 cells Male0.3 ± 0.30.13
(percentage of CD20+ cells)Female0.2 ± 0.3
Table
Table 2. Relative amounts of T lymphocyte subpopulations with the mean and standard deviation [%]. Group differences were assessed using the Mann–Whitney U test.
Table 2. Relative amounts of T lymphocyte subpopulations with the mean and standard deviation [%]. Group differences were assessed using the Mann–Whitney U test.
nSexMean ± Standard Deviation [%]p-Value
Th cells16Male74.4 ± 6.60.22
(percentage of CD3+ cells)21Female76.8 ± 7.2
Cytotoxic T cells16Male27.9 ± 7.60.12
(percentage of CD3+ cells)21Female24.2 ± 7.7
Th cells with αβ-TCR CD4+ CD3+16Male76.0 ± 6.40.5
(percentage of TCR αβ + cells)21Female77.3 ± 7.1
Activated cytotoxic Th-cells with αβ-TCR16Male0.6 ± 0.60.27
(percentage of TCR αβ + cells)21Female0.9 ± 0.8
Memory effector Th cells16Male49.5 ± 13.60.48
(percentage of CD3+ CD4+ cells)21Female52.1 ± 15.8
Memory central Th cells16Male5.7 ± 2.80.58
(percentage of CD3+ CD4+ cells)21Female6.7 ± 4.1
Naïve effector Th cells16Male40.9 ± 15.20.17
(percentage of CD3+ CD4+ cells)21Female34.9 ± 11.8
Naïve central Th cells16Male3.9 ± 1.40.62
(percentage of CD3+ CD4+ cells)21Female6.4 ± 9.4
Memory effector cytotoxic T cells16Male50.8 ± 13.80.4
( percentage of CD3+ CD8+ cells)21Female53.7 ± 14.1
Memory central cytotoxic T cells16Male6.2 ± 4.30.66
(percentage of CD3+ CD8+ cells)21Female7.8 ± 6.4
Naïve effector cytotoxic T cells16Male39.4 ± 14.60.24
( percentage of CD3+ CD8+ cells)21Female34.1 ±1 0.6
Naïve central cytotoxic T cells16Male3.6 ± 1.60.73
(percentage of CD3+ CD8+ cells)21Female4.5 ± 4.1
Naïve thymus negative Th cells16Male24.4 ± 9.80.005
(percentage of CD3+ CD4+ cells)21Female15.9 ± 5.7
Naïve thymus-positive Th cells CD31+16Male65.7 ± 9.40.055
(percentage of CD3+ CD4+ cells)21Female70.8 ± 9.6
Th1 cells11Male2.8 ± 1.60.61
(percentage of CD3+ cells)16Female2.8 ± 1.9
Naïve Th1 cells11Male87.2 ± 7.00.54
(percentage of CD3+ CD4+ CD183+ CD196+ cells)16Female88.1 ± 6.8
Memory Th1 cells11Male12.8 ± 7.00.51
(percentage of CD3+ CD4+ CD183+ CD196+ cells)16Female11.9 ± 6.8
Th2 cells11Male0.7 ± 0.50.54
(percentage of number of CD3+ cells)16Female0.5 ± 0.3
Naïve Th2 cells11Male66.8 ± 8.60.9
(percentage of CD3+ CD4+ CD294+ CD194+ cells)16Female67.6 ± 11.2
Memory Th2 cells11Male33.2 ± 8.60.9
(percentage of CD3+ CD4+ CD294+ CD194+ cells)16Female32.4 ± 11.2
Regulatory T cells11Male2.3 ± 0.60.8
(percentage of CD3+ cells)16Female2.4 ± 0.7
Table
Table 3. Definition of B and T lymphocyte subpopulations according to surface markers.
Table 3. Definition of B and T lymphocyte subpopulations according to surface markers.
Lymphocyte SubsetsDefinition
B lymphocytesB cellsCD19+
Innate B cellsCD19+ CD27− IgD− IgM−
Naïve B cellsCD19+ CD27− IgD+ IgM+
Memory B1 cellsCD19+ CD27+
Marginal zone memory B cellsCD19+ CD27+ IgD+ IgM+
Class-switched memory B cellsCD19+ CD27+ IgD− IgM−
Late memory B cellsCD19+ CD27+ CD38+ IgM+
PlasmablastsCD19+ CD27+ CD38++ IgM−
Transitional B cellsCD19+ CD20+ CD27− CD38+
B1 cellsCD20+ CD27+ CD43+
B2 cellsCD20+ CD27+ CD43−
T lymphocytesT cellsCD3+
T helper cellsCD3+ CD4+
Cytotoxic T cellsCD3+ CD8+
T helper cells with αβ-TCRTCRαβ+ CD4+
Cytotoxic T helper cells with αβ-TCRTCRαβ+ CD8+
Activated T helper cells αβ-TCRTCRαβ+ CD4+ CD69+
Activated cytotoxic T helper cells with αβ-TCRTCRαβ+ CD8+ CD69+
Memory effector T helper cells CD3+ CD4+ CD62L− CD45RO+
Memory central T helper cellsCD3+ CD4+ CD62L+ CD45RO+
Naive effector T helper cellsCD3+ CD4+ CD62L− CD45RO−
Naive central T helper cellsCD3+ CD4+ CD62L+ CD45RO−
Memory effector cytotoxic T cellsCD3+ CD8+ CD62L− CD45RO+
Memory central cytotoxic T cellsCD3+ CD8+ CD62L+ CD45RO+
Naïve effector cytotoxic T cellsCD3+ CD8+ CD62L− CD45RO−
Naïve central cytotoxic T cellsCD3+ CD8+ CD62L+ CD45RO−
Naïve thymus negative T helper cellsCD3+ CD4+ CD31− CD45RO−
Naïve thymus positive T helper cellsCD3+ CD4+ CD31+ CD45RO−
T helper cells 1CD3+ CD4+ CD183+ CD196+
Naive T helper cells 1CD3+ CD4+ CD183+ CD196+ CD45RO−
Memory T helper cells 1CD3+ CD4+ CD183+ CD196+ CD45RO+
T helper cells 2CD3+ CD4+ CD194+ CD294+
Naïve T helper cells 2CD3+ CD4 + CD45RO− CD194+ CD294+
Memory T helper cells 2CD3+ CD4+ CD45RO+ CD194+ CD294+
Regulatory T cellsCD3+ CD4+ CD25+ CD127−
Table
Table 4. Antibodies used for immunophenotyping.
Table 4. Antibodies used for immunophenotyping.
MarkerFluorophoreCloneVendorCatalogPanel
CD127Alexa-Fluor 647HIL-7R-M21BD 55,8598T cells-panel 2
CD183BV480CXCR3BD 74,6283T cells-panel 2
CD19APC-R700HIB19BD 56,4977B cells-panel 1
CD194 (CCR4)PE1G1BD 55,1120T cells-panel 2
CD196 (CCR6)APC-R700CCR6BD 56,5173T cells-panel 2
CD20BB7002H7BD 74,5889B cells-panel 1
CD21BV421B-Ly4BD 56,2966B cells-panel 1
CD25BV421M-A251BD 56,2442T cells-panel 2
CD27APCL128BD 33,7169B cells-panel 1
CD294 (CRTH2)BV650BM16BD 74,0616T cells-panel 2
CD3BV786SK7BD 56,3800T cells-panel 1
T cells-panel 2
CD31BV421L133.1BD 74,4801T cells-panel 1
CD38PEHB-7BD 34,5806B cells-panel 1
CD4PE-CF594SK3BD 56,6317T cells-panel 1
T cells-panel 2
CD43BV6051G10BD 56,3378B cells-panel 1
CD45ROBV605UCHL1BD 56,2791T cells-panel 1
T cells-panel 2
CD5BV650L17F12BD 74,2551T cells-panel 1
CD62LBB700SK11BD 74,5995T cells-panel 1
CD69BV480FN50BD 74,7519T cells-panel 1
CD8APC-R700SK1BD 56,5192T cells-panel 1
IgDPE-CF594IA6-2 BD 56,2540B cells-panel 1
IgMBV480G20-127BD 56,6146B cells-panel 1
TCRαβ FITCWT31BD 33,3140T cells-panel 1
TCRγδPE11F2BD 33,3141T cells-panel 1
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Bous, M.; Schmitt, C.; Hans, M.C.; Weber, R.; Nourkami-Tutdibi, N.; Tenbruck, S.; Haj Hamoud, B.; Wagenpfeil, G.; Kaiser, E.; Solomayer, E.-F.; et al. Sex Differences in the Frequencies of B and T Cell Subpopulations of Human Cord Blood. Int. J. Mol. Sci. 2023, 24, 11511. https://doi.org/10.3390/ijms241411511

AMA Style

Bous M, Schmitt C, Hans MC, Weber R, Nourkami-Tutdibi N, Tenbruck S, Haj Hamoud B, Wagenpfeil G, Kaiser E, Solomayer E-F, et al. Sex Differences in the Frequencies of B and T Cell Subpopulations of Human Cord Blood. International Journal of Molecular Sciences. 2023; 24(14):11511. https://doi.org/10.3390/ijms241411511

Chicago/Turabian Style

Bous, Michelle, Charline Schmitt, Muriel Charlotte Hans, Regine Weber, Nasenien Nourkami-Tutdibi, Sebastian Tenbruck, Bashar Haj Hamoud, Gudrun Wagenpfeil, Elisabeth Kaiser, Erich-Franz Solomayer, and et al. 2023. "Sex Differences in the Frequencies of B and T Cell Subpopulations of Human Cord Blood" International Journal of Molecular Sciences 24, no. 14: 11511. https://doi.org/10.3390/ijms241411511

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop