Journal of Immunology Research

Journal of Immunology Research / 2019 / Article
Special Issue

Tissue-Specific Immunity in Homeostasis and Diseases

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Review Article | Open Access

Volume 2019 |Article ID 7693183 | 13 pages |

Immunity in the Cervix: Interphase between Immune and Cervical Epithelial Cells

Academic Editor: Ning Wu
Received03 Dec 2018
Revised08 Feb 2019
Accepted25 Feb 2019
Published17 Apr 2019


The cervix is divided into two morphologically and immunologically distinct regions, namely, (1) the microbe-laden ectocervix, which is proximal to the vagina, and (2) the “sterile” endocervix, which is distal to the uterus. The two cervical regions are bordered by the cervical transformation zone (CTZ), an area of changing cells, and are predominantly composed of cervical epithelial cells. Epithelial cells are known to play a crucial role in the initiation, maintenance, and regulation of innate and adaptive response in collaboration with immune cells in several tissue types, including the cervix, and their dysfunction can lead to a spectrum of clinical syndromes. For instance, epithelial cells block progression and neutralize or kill microorganisms through multiple ways. These (ways) include mounting physical (intercellular junctions, secretion of mucus) and immune barriers (pathogen-recognition receptor-mediated pathways), which collectively and ultimately lead to the release of specific chemokines and or cytokines. The cytokines subsequently recruit subsets of immune cells appropriate to a particular immune context and response, such as dendritic cells (DCs), T, B, and natural killer (NK) cells. The immune response, as most biological processes in the female reproductive tract (FRT), is mainly regulated by estrogen and progesterone and their (immune cells) responses vary during different physiological phases of reproduction, such as menstrual cycle, pregnancy, and post menopause. The purpose of the present review is to compare the immunological profile of the mucosae and immune cells in the ecto- and endocervix and their interphase during the different phases of female reproduction.

1. Introduction

The female reproductive tract (FRT) can be divided into two immunological regions, namely, the upper (endocervix, uterus, and oviduct) and lower (vagina and ectocervix) FRT [1]. While the lower FRT is associated with a heavy microbial presence, the upper area is considered “sterile,” although this theory has been recently challenged [2] (Figures 1 and 2). Thus, each of the two regions has unique tissue-specific immunological features and they both undergo specific alterations during different physiological conditions (menstrual, pregnancy, postpartum, and age), and collectively, they create an immune response spectrum with two “opposite” ends [3]. On one end of the spectrum, an immune response essential for protection against infection and other noxious environmental insults is generated. On the other end of the spectrum, and simultaneously, a symbiotic mutualism with commensal microbes and immunological tolerance to allogenic sperm, as well as semiallogeneic fetus, is maintained during pregnancy [3]. These complex immune responses are largely orchestrated and regulated by the sex steroid hormones, and dysregulation of these immune responses can lead to various clinical complications, such as bacterial vaginosis, vaginal candidiasis, cervical cancer, urinary tract infections, and preterm labor [4, 5]. The present review largely focuses on the tissue-specific immunological alterations that take place in the ecto- and endocervix under different physiological conditions.

The human cervix is a barrel-shaped structure with a central canal and measures approximately 2 cm long. The proximal end of the cervix is called internal os and opens into the uterus without any obvious features to mark the borders of the two tissues, whereas the distal end is called external os and opens into the vagina [6]. The cervical tissue has two dominant cell types in both endo- and ectocervix consisting of (a) stromal and (b) epithelial cells. These two cell types are separated by a basement membrane [7]. The stromal tissue is predominantly made up of fibroblasts, with smooth muscle, and scattered immune cells, embedded in a collagen-rich extracellular matrix containing hyaluronan and proteoglycans [8]. The present review focuses on the two cell types that play a predominant role in local immune responses, namely, the cervical epithelial and immune cells. Overall, both the cervical epithelial and immune cells from the ecto- and endocervix protect the upper FRT from bacterial infiltration through various mechanisms. (a) The cervical epithelial cell mounts a physical barrier through mucus and epithelial sheets. These cells (epithelial) also generate specific immune responses and collaborate with regular immune cells. (b) The immune cells (resident and nonresident) orchestrate both innate and adaptive immune responses [3, 9, 10].

2. The Multi-Immune Facets of Cervical Epithelial Cells

2.1. General Overview

Epithelial cells are the “first responders” to come in direct contact with potential pathogens that infiltrate the FRT. As such, they have to be flexible, nimble, and adaptive. Also, an effective communication between epithelial and immune cells is critical in mounting an effective protection against infection. For instance, FRT epithelia, including that of the cervix, are capable of mounting diverse innate and adaptive immune functions. Essentially, the cervical epithelial cells have several immune capabilities that are used to block ascension of pathogens to the upper FRT. Notably, these include (1) mounting a physical immune barrier, (2) secreting antimicrobial, cytokine, and chemokine factors, and (3) exhibiting some of the more specialized innate and adaptive immune functions, such as antigen presentation.

2.2. Cervical Epithelial Cell Mounts Physical Barrier against Pathogens

The upper FRT is lined with a single layer of columnar cells, while the ectocervix has a stratified layer of cells covered by squamous epithelial cells. The two types of epithelia (ecto versus endo) are separated by a junction with squamocolumnar cells. The barrier properties of the mucosal epithelia are regulated in part by adhesion molecules which seal off the intercellular space between adjacent cells [11]. Thus, the integrity of epithelial barrier is maintained by intercellular junctions that prevent the invasion of microbes. The intercellular junctions present in the lateral membrane of epithelial cells can be classified into three main types, namely, tight or occluding junctions, adherent junctions (including desmosome and hemi-desmosomes), and gap junctions (communicating junctions). The second physical barrier mounted by the cervical epithelia is the secreted mucus [12].

2.2.1. Cell Junctions in the Cervical Epithelia

An electron microscopy study has demonstrated that classical tight junctions comprise the principal intercellular junctions between the simple columnar epithelial cells in the endocervix [13, 14]. In contrast, the uppermost layers of the stratified squamous ectocervical epithelium are devoid of organized intercellular junctions [13, 14]. Moreover, junctional molecules thought to be key regulators of epithelial permeability, junctional integrity, and leukocyte infiltration, such as F11R (or JAM-A), E-cadherin, occludin, claudin-1, and TJP1 (or ZO-1), are abundant in the human endocervix [13]. A lack of tight junctions in the lower FRT does not only allow movement of small molecules and pathogens between epithelial cells but also enables immune cells, such as epithelial cervicovaginal Langerhans cells or dendritic cells (DC), to do the same. Unsurprising is the fact that the ectocervix and the vagina share a continuous morphologically identical mucosa layer, and therefore, the distribution of junctional molecules is similar in both tissues. According to Blaskewicz et al., the most robust junctions in the stratified squamous epithelium of the ectocervix and vagina lie in the parabasal epithelium, just above the basal layer in contact with the basement membrane [13]. Adherent junctions were particularly abundant within these cells. The integrity of the junctions progressively lessens toward the apical surface, where epithelial cells become cornified, lose all cellular contacts, and are sloughed into the lumen [13]. The structure of tight junctions is affected by hormones [15] as well as cytokines [11]. For instance, our group has demonstrated that exogenous vascular endothelial growth factor (VEGF), a potent angiogenic factor, promotes paracellular permeability in cervical epithelial cells during pregnancy [16]. Besides, tumor necrosis factor-α (TNF-α), a signaling molecule, decreases transepithelial resistance in uterine epithelial cells [17]. The presence of gap junctions in cervical epithelial cells has been scarcely studied [18, 19] (Figures 1 and 3).

2.2.2. Mucus as the Second Physical Barrier with Antimicrobial Activity

The cervical mucus is produced by goblet cells from pseudoglands and undergoes marked modifications that results in signature biochemical and biophysical characteristics at different stages of the cycle [12, 20]. Mucus is a mixture of various factors whose composition and concentration vary across the cycle and during pregnancy. These factors include water, lipids, cholesterol, carbohydrates, inorganic ions, and proteins (immunoglobulins, plasma proteins, mucins, and enzymes) [12]. The changes in mucus consistency during the menstrual cycle and or pregnancy vary mucus’s ability to physically block ascendancy of bacteria while permitting entry of sperm to the upper FRT. For instance, the upper FRT is vulnerable to infection during menstruation and childbirth when the cervix opens to allow passage of menstrual flow and the baby. Therefore, the immune response generated by the cervix has to be flexible and nimble under the varying physiological reproductive conditions, enabling the cervix to play various key roles in female reproduction, notably being the key immune “gate keeper” of the “sterile” upper FRT (Figure 4).

Mucins are large glycoproteins that serve as the gel or glue of the mucus and are, therefore, able to entrap and immobilize pathogens, among other things, depending on the thickness of the mucus [20]. There are more than 20 different mucins and are differentially expressed by goblet cells depending on the location and menstrual status [20]. MUC4 and MUC5 (5AC, 5B) and MUC6 are the major mucin proteins of the endocervical mucus, and their quantity changes during the cycle [21]. Overall, the cervical mucus acts as a semipermeable and antimicrobial barrier, preventing access of pathogens to the upper genital tract while simultaneously permitting sperm entry prior to ovulation [20, 21] (Figure 4).

The antimicrobial and immune constituents of mucus compliment the physical barrier mounted by cervical mucus. These constituents cited earlier include immunoglobulins, complement, antibodies, cytokines, antimicrobial proteins, and immune cells [22], and their concentrations or levels display cyclic fluctuations [22, 23], whereas other molecules, such as IL-6, IL-4, IL-12, IFN-γ, and T cell activity, do not have cyclic variation [23, 24]. While these cyclic variation in mucus composition increases vulnerability of the upper FRT as they may result in ascendance of pathogens, the thinning of the mucus during ovulation also allows for easier passage of sperm [12]. The combination of a physical and immune barrier mounted by the mucus and epithelial sheet is perhaps compensatory and potentiate the immune function by for instance slowing particle diffusion while allowing time for biological defense [12].

2.3. Cervical Epithelial Cells Secrete Antimicrobial, Cytokine, and Chemokines

Epithelial cells are known to secrete a concoction or cocktail of regulatory factors that either synergize or complement each other, such as cytokines and chemokines and a spectrum of antimicrobials, including lactoferrin, lysozyme, complement, and defensins, along with immunoglobulins A (IgA) and IgG that confer protection against pathogens [2527]. For instance, the secretion of antimicrobial molecules in the cervical mucus provides an interesting example of the synergy or interdependence between the innate and adaptive immune functions. Several species of bacteria in the mouse uterine lumen bind complement C3 produced by epithelial cells, which (complement C3), in turn, facilitates the binding of IgA and IgG antibodies to the bacteria, ultimately leading to a more efficient phagocytosis of bacteria by neutrophils [28]. Therefore, while the production of complement components is an innate process, the antibodies are part of the adaptive process that leads to protection [9]. It has been shown that the expression of IgA and IgG in uterine tissue is hormonally regulated [27]. The distribution of complement receptor 3 (CR3) on the epithelia of the human female genital tract has been described previously, as well as the production of alternative complement components in primary human ecto- and endocervical cells, which subsequently allows C3b deposition and its rapid conversion to iC3b [2932].

Generally, there appears to be a distinction in the composition of the antimicrobial of the lower FRT compared to the upper FRT, a likely reflection of the unique functions of the two tracts [4]. For instance, the upper FRT epithelial cells secrete a battery of antimicrobial peptides, such as human β-defensins (hBDs), secretory leukocyte protease inhibitor (SLPI), lysozyme, tracheal antimicrobial peptide, macrophage inflammatory protein-3 (MIP3α/CCL20), trappin-2/elafin, and cathelicidin [14], whereas the proteomic profile of the pathogen-laden lower FRT includes SLPI, hBD-2, human neutrophil peptide 1 (HNP1), HNP2, HNP3, lysozyme, lactoferrin, surfactant A, and elafin (also known as peptidase inhibitor 3) [4, 33] (Figure 5). Other common cervical secretions include cytokines, such as IL-1β, IL-6, IL-10, IL-18, CC-chemokine ligand 2 (CCL2), and vascular endothelial growth factor (VEGF), whose levels are markedly higher in the lower FRT, while IL-12, IL-15, macrophage migration inhibitory factor (MIF), and dickkopf homolog 1 (DKK1) levels are very low in cervical secretions compared to endometrial secretions [25]. Cytokines modulate diverse physiological, inflammatory, and noninflammatory processes and development, but they also modulate paracellular permeability by restructuring tight junctions through a variety of different signaling pathways. For example, the proinflammatory cytokine tumor necrosis factor alpha (TNF-α), transforming growth factor beta (TGF-β), and hepatocyte growth factor (HGF) directly impaired tight junctions in a number of epithelial and endothelial cell lines [11], including uterine epithelium [17]. Recently, the current theory on the immune specificity and distinctiveness between the two compartments of the FRT has been challenged [34] since many of the proteins differentially secreted in the upper and lower FRT, such as CCL2, IL-6, IL-10, IL-15, and IL-1β, are also involved in immune cell migration and phenotype development [25]. Consequently, the observed differences in the secretion of specific proteins may regulate the variations in immune cell populations across the FRT [4] (Figures 6 and 7).

2.4. Cervical Epithelial Cell as an Antigen-Presenting Cell

A typical antigen-presenting cell (APC) has a major histocompatibility complex (MHC) class II molecule located on its surface and exposes a processed antigen to CD4+ T cell, which is the basis for driving T cell activation, proliferation, and differentiation into effector cells [35]. APCs are bone marrow-derived and include dendritic cells, macrophages, and monocytes [36]. However, other cell types with demonstrated antigen-presenting capacity include skin Langerhans cells, liver Kupffer cells, and spleen dendritic cells [36]. Antigen presentation by epithelial cells has been demonstrated at several mucosal surfaces, including uterine epithelial cells [37], as well as in uterine stroma and vagina [35]. Within the FRT, epithelial cells express MHC class II molecules [37, 38]. Sex hormones may play a role in regulating antigen presentation [38], which is also regulated by epithelial cell-derived cytokine, as demonstrated by the fact that uterine epithelial cells produce transforming growth factor-β (TGF-β) that suppresses underlying APCs in the uterine stroma, in response to estradiol (E2) [39].

2.5. Cervical Epithelial Cells Express Various Pattern Recognition Receptors

We have described earlier how the epithelia of the FRT play a role against pathogens by (a) mounting a physical barrier formed by cell junctions and secreting mucus containing specific proteins, (b) secreting cytokines, chemokines, and antimicrobials, and (c) as antigen-presenting cells. Cervical epithelial cells also recognize pathogen-associated molecular patterns (PAMPs) on microbes (bacteria, parasites, and viruses) through pattern recognition receptors (PRR) such as toll-like receptor (TLR) family, retinoic acid-inducible gene 1 (RIG-I)-like receptors (RLRs), and NOD-like receptors (NLRs) [4042]. TLR2 and TLR4 detect signals from gram-positive and gram-negative bacteria, respectively [4042], while NOD1 and NOD2 mediate signals from peptidoglycan moieties derived from gram-positive and gram-negative bacteria, as well as from nonbacterial pathogens, such as viruses and protozoan parasites [43]. RLRs mediate signals from a variety of viruses which leads to the production of IFN-1 and induction of antiviral responses [44]. The level of expression of these receptors is higher in the upper FRT, considered “sterile” compared to the lower FRT, which is pathogen-laden [4, 40]. Specific bacteria-derived ligands (peptidoglycan, lipopolysaccharide) bound to TLR increase the expression of inflammation mediators, such as cytokines and chemokines (mentioned before) [40]. Further, it has been shown that E2 alters the profile of cytokine secretion in cultured cervical epithelial cells when TLR2 and TLR4 signaling pathways are activated [40, 42], and the nature of the response varies based on the type of cytokine and duration of the coincubation of cells with E2 and TLR ligands [40]. The authors conclude that a complex immune-modulatory role of E2 exists at the epithelial surface and that such a role likely enables the mucosal layer of the lower FRT to discriminate between commensals and pathogens and mount appropriate host defense against ascending infection [40]. By contrast, TLR7, TLR8, and TLR9 are evenly expressed throughout the upper and lower FRT. These receptors detect single-stranded RNA (TLR7 and TLR8) and DNA (TLR9). However, the exact signaling mechanisms remain to be elucidated.

2.6. The Vaginal Microbiome

The vagina has been compared to a nutrient-rich chamber for microbes [45]. These microbes composed of different species (bacteria, viruses, fungi, and protozoa) play a critical role in maintaining the overall health of the vagina and prevent infections [4547]. Disruption of this microbial community could lead to vaginal infections, as well as other urogenital complications and adverse pregnancy outcomes, among others [45, 48]. Factors that can change the composition of vaginal microbiota are diverse and include age, hormonal levels, genital infections, and hygiene practices [45, 49]. To date, more than 50 microbial species have been described in the vaginal tract, dominated by Lactobacillus species (70% of the total) [50]. The key members of the lactobacillus species include L. crispatus, L. gasseri, L. inners, and L. jensenii [46]. This species (Lactobacillus) has received considerable attention because of their protective and probiotic properties [51], which in part is exerted by producing factors that lower pH below 4.5 and inhibit overgrowth of normal facultative anaerobes, namely, lactic acid [5255]. Other key species found in the vagina include anaerobes (Gardnerella, Atopobium, Mobiluncus, Prevotella, Streptococcus, Staphylococcus, Ureaplasma, and Megasphaera) and commensal microorganisms, such as the opportunistic fungus, Candida albicans [56]. Further studies are needed to understand the underlying mechanism of the interdependence between the FRT microbiota and the host, which will be critical in promoting the reproductive health of women.

3. Region-Specific Distribution and Function of Immune Cells in the Mucosae of the Cervix

3.1. General Overview

As stated earlier, the vagina and ectocervix, which constitute the lower FRT, are characteristically heavily laden with microbes because they are directly exposed to the external environment, in contrast to the “sterile” upper FRT. As such, it should be expected that these two regions will have different immunological profiles. Further, immune cells in the two regions are overall believed to be primarily regulated by sex hormones during menstrual cycle [4], pregnancy, and postpartum [10] in a site-specific manner, which is dependent on the type of factors present in the local tissue microenvironment, such as growth factors, cytokines, and chemokines [4, 10]. Generally, consistent with mucosae of other tissues of the body, T lymphocytes are much more abundant than B cells in the mucosae of the human cervix [57, 58], and approximately 40% of the cervical T cells are CD4+ T cells, the other 60% being CD8+ T cells [58]. Within the CD4+ T cells located in the cervix, the majority (70%) exhibit an effector memory or effector phenotype, compared to about 60% of the CD8+ expressing an effector cell phenotype, which is consistent with the cervix being an effector site for cell-mediated immunity and the tissue residency of cervical CD4+ and CD8+ T cells [10, 58]. In contrast, natural killer (NK) cells are only 2.7% of the CD45+ of total immune cells [3] and CD19+ B cells are only 0.9% of the immune cells [3, 58]. However, while Trifonova et al. attest that CD8+ T cells are more numerous than CD4+ T cells, the specific local distribution of CD4+ and CD8+ T cells is still debatable [58]. The discrepancies between some studies in the specific proportion of each leukocyte population could, in part, be attributed to the differences in the experimental designs of the studies [57, 58], such as reproductive phase (menstrual cycle vs. menopausal vs. gestation) and sample size [3].

Macrophage, dendritic cells (DCs), and other lymphocyte lineage-negative cells (CD3, CD20, CD56, and CD16) are the major immune cells in the cervix, ranging from 37 to 55% of CD45+ mononuclear cells [58]. CD11+ macrophages are the dominant cells at approximately 30% of CD14+ cells in the cervix. The cervical DCs are slightly more prevalent than peripheral blood DCs, which are less than 1% of CD45+ cells [58].

3.2. Immune Cells in the Mucosae of the Ectocervix

T cells (CD3+) are the most abundant leukocytes in the FRT and are concentrated more in the lower FRT than the upper FRT [4]. In the lower FRT, most T cells are believed to have effector memory phenotype [58] and 35% of CD45+ mononuclear cells are CD3+ T cells. Also, CD4+ T and CD1a+ immature DCs are significantly more abundant in the ectocervix than in the vagina [58]. On the other hand, the CD4+ and CD8+ T cells are equally abundant in the ectocervix, in contrast to the endometrium where CD8+ T cells predominate [4]. Although NK and B cells are also present in the ectocervix, they are much less prevalent than T cells [4]. NK and granulocytes (CD66b+) are more abundant in the upper FRT than in the lower FRT [4]. Both T and B cells are more abundant in the ectocervix than the endocervix, correlating positively with the microbial load [10, 58] (Figure 8).

Because the number of CD8+ T, B, and NK cells decrease after menopause, immune cells in the human cervix are likely regulated by hormones [59]. Myeloid APCs are also prevalent in both the human ecto- and endocervix [10]. In the APC compartment, CD14+ cells are the most abundant, with the largest populations being CD11c- macrophages followed by CD11c+ cells, which encompass tissue DCs and/or monocytes that have not yet been fully differentiated into macrophages [58]. Conventional DC subsets are also detected in the CD14- subset of APCs; however, their abundance, although greater than in the peripheral blood, is much lower than that of the CD14+ cells [58]. Despite the characterization of these human cervical immune cells, the underlying regulatory mechanisms of their differentiation and functions by systemic and local immune signals remain to be studied. The fact that Pudney et al. were able to detect higher concentrations of CD8+ and TIA1+ T lymphocytes in the ectocervix and cervical transformation zone (CTZ) suggests that these could be major effector sites of cytotoxic T lymphocyte responses [60]. Also, because the ectocervix and CTZ contain the highest number of antigen-presenting cells, they could also likely be the best location for the induction of cell-mediated immune responses in the lower FRT [60]. Although B cells are a minor cell population throughout the female reproductive tract, IgG- and IgA-producing plasma cells are predominantly localized in the cervix and, to a lesser extent, the vagina. Specifically, cervicovaginal secretions are characterized by greater amounts of IgG than IgA, and both are hormonally regulated [14].

DCs are the most potent antigen-presenting cells and as such play a major role in the uterine defense [61] by activating naïve T cells, an essential step in initiating adaptive immune response [61]. DCs have been predominantly seen in the basal and suprabasal regions, and their dendritic nature was more prominent in the basal layers of the stratified squamous epithelia of the ectocervix and the CTZ [61]. DCs have also been described in the intermediate layer with no typical dendritic processes [62]. Although the specific function of these cells remain unknown, Rabi et al. have proposed that they maybe nondendritic accessory antigen-presenting cells [62]. The distribution of DCs in the subepithelium is not uniform, and they (DCs) migrate from this location to the epithelium where they encounter the antigens [62].

3.3. Immune Cells in the Cervical Transformation Zone (CTZ)

The CTZ represents an abrupt transition between the immunologically distinct regions of the lower and upper FRT, namely, the ecto- and endocervix [60, 63]. It (CTZ) appears to be an immunocompromised region as it is a site of multiple pathogenic conditions, including HIV and metaplastic squamous epithelium, which both develop at the squamocolumnar junction. It is, therefore, rather surprising that few studies have specifically examined cells from this immunologically strategic region. Indeed, it has been shown as a preferential localization of lymphocytes and APCs to the cervical CTZ, in essence, mounting the “last” line of defense and “drawing the line” between the pathogen-laden ectocervix (lower) and the “sterile” endocervix (upper FRT) [60]. Specifically, it has been shown that CD8+ and TIA1+ T cells accumulate in the CTZ, implying that the CTZ functions as the “last” immunological barrier to ascending microbes. However, and surprisingly, this site, which has a higher concentration of CD4+, is the preferred site of HIV-1 infection [60] and greater than 90% of cervical cancers originate from it [64]. It is still unclear why such an immune cell-rich region and strategic immunological “border” or landmark is highly susceptible to diseases and malignant tumor (Figure 8).

3.4. Immune Cells in the Mucosae of the Endocervix

The population density of T cells and macrophages in the endocervix is much lower than that of the ectocervix, where CD8+ predominates [4, 60]. The endocervix contains numerous IgA+ and IgM+ plasma cells that mediate humoral immune response [60]. Furthermore, no CD1A+ dendritic cells are observed or localized in the epithelia, glands, or lamina propria of the endocervix [60]. Also, interestingly, no differences were observed in the number and pattern of leucocyte localization during the proliferative versus secretory phases of the menstrual cycle or in postmenopausal women [60]. Nonetheless, sex hormones are believed to influence the functions of immune cells [60] (Figure 8).

As stated earlier, the ecto- (or lower FRT) and endocervix (or upper FRT) are two immunologically distinct regions, with some variation in the profile of immune cell subpopulations. For instance, CD3+ and B cells are twice as much in the ectocervix compared to the endocervix [58], and additionally, both CD4+ and CD8+ T cells are more prevalent in the ectocervix than the endocervix [58]. However, there are also some similarities between the two regions. For instance, the number of NK cell subsets of CD56brightCD16- and CD56dimCD16+ is not significantly different between the endo- and ectocervix, and generally, the IL-22-producing NK cells, known to play a key role in mucosal immunity, are very rarely detected in the cervix [58]. A summary of the review is provided in Figure 8.

4. Immune Profile in the Ecto- and Endocervix during Different Reproductive Phases

4.1. General Overview

Estradiol (E2) and progesterone (P), which are secreted by the ovaries during menstrual cycle and pregnancy, are the primary regulators of the cellular function (epithelial, fibroblasts, myometrial, and immune) of the FRT [57, 65]. The immune cells, which include natural killer (NK) cells, macrophages, dendritic cells, and T cells, are the main cells responsible for fighting infections, while simultaneously ensuring a successful conception and subsequent development and birth of the fetus [4, 40, 66]. Specifically, the immunological effects of the two hormones (E2 and P) are contradictory, i.e., while P exerts anti-inflammatory effects by inducing the transcription of proteins and growth factors that mitigate inflammation and promote repair in mucosae [66], E2, on the other hand, regulates the activity of different inflammatory transcriptional factors, such as AP-1, SP1, STAT, and vitamin D receptor in human uterine cells [44], as well as alters the immune response of cervical epithelial cells [40].

4.2. Menstrual Cycle

The menstrual cycle is divided into two main phases: (1) the proliferative (FRT) or follicular phase (ovarian) and (2) the secretory (FRT) or luteal phase (ovarian) [67]. As stated earlier, the changes and fluctuations in hormonal levels during the menstrual cycle have a profound region-specific effect on the functional status of the immune system of the FRT, including the cervix [4].

For instance, at midcycle (ovulation), when E2 levels are high, the production of antimicrobial peptides is inhibited in the lower FRT, thus creating a window of vulnerability for infection [68]. On the other hand, the activity of cytotoxic cells in the upper FRT is reduced at a time when the production of antimicrobial peptides is enhanced, thus optimizing conditions for successful implantation [58, 68]. Furthermore, during the proliferative stage of the menstrual cycle (prior to ovulation), cervical/vaginal secretions contain higher levels of antimicrobial peptides compared to other phases of the cycle [68], thus complementing and reinforcing its defense barrier capabilities against microorganisms, besides its immunomodulatory effects.

The proliferative phase is also characterized by angiogenesis and the regeneration of the endometrial and cervical tissue and the concentration of immune cells in the endometrium diminish during this time [65]. In contrast, in the lower FRT, fluctuations in the levels of sex hormones do not affect the number of immune cells, which remain constant throughout the cycle [60]. Around the midcycle, when uterine angiogenesis peaks, recruitment of innate immune cells such as NK cells, neutrophils, and macrophages in the uterus is facilitated [4]. This recruitment is mediated by cytokines, chemokines, and growth factors, which are mainly produced by uterine endometrial cells and fibroblasts under the influence of both sex steroids [65]. Overall, 40-50% of leukocytes in the FRT are T cells [57, 58, 69], and during the proliferative phase, most T cells in the endometrium are dispersed or are concentrated in small aggregates in the stroma or as epithelial lymphocytes [4]. Lymphoid aggregates (LA) structurally have a core of B cells in the center surrounded by CD8+ T cells and encapsulated by macrophages [70]. These immunoaggregates are formed in the endometrium but not in the ectocervix or the lower FRT, in the absence of an infection [70]. They (LAs), however, peak in size midcycle and persist during the secretory phase and may provide protection against secondary infections or may play a role in maintaining the T cell repertoire and prevent the loss of resident memory cells during menstruation [4, 70].

During the late secretory phase and menstruation, which is associated with a decrease in sex steroids and subsequent initiation of inflammatory response, the number of immune cells increases in the endometrium [57, 65, 71]. These inflammatory responses include decreased prostaglandin metabolism, loss of protection from reactive oxygen species (ROS), and increased synthesis of proinflammatory prostaglandins, cytokines, chemokines, and matrix metalloproteinases (MMP), which result in recruitment of leukocytes. Collectively, these actions lead to tissue breakdown and the characteristic bleeding associated with menstruation [71].

Macrophages on the other hand only represent about 10-20% of the FRT leukocytes [4, 57, 58]. However, they are more abundant in the stroma of the endometrium than the endocervix or the ectocervix, and their number remains stable during the proliferative phase [4]. Uterine NK cells represent around 30% of leukocytes during the window of implantation and increase in number during the secretory phase and populate the endometrium before pregnancy [65, 72]. It is still unclear how exactly the number of NK cells increases [4]. Overall, a plethora of immune cells, including neutrophils, NK cells, macrophages, eosinophils, and DCs, migrate into the uterus in response to hormonal changes [71, 73]. For instance, P withdrawal triggers menstruation and an inflammatory response in the endometrium, leading to an influx of leukocytes that mediate tissue breakdown and repair [4].

4.3. Postmenstrual Cycle

During menopause, the fluctuation of sex hormones declines and their levels remain low and constant [74]. These hormonal alterations lead to various changes, notably a progressive dysregulation of the systemic immune system that leads to increased susceptibility to infections and malignancies and reduced responses to vaccination and increased general inflammation [75]. Moreover, women appear to lose their immunological advantage after menopause, since in aging, they are more susceptible to infections and to develop inflammatory diseases [68]. The specific changes in the systemic immune system include a decreased CD4+ : CD8+ cell ratio, increased number of differentiated effector and memory T cells, depletion of naive T cells, and decreased frequency of B cells [75]. Natural killer (NK) cells, which fight against viral pathogens and tumors, increase with age [75]. However, they (NK cells) exhibit a decrease in cytotoxicity and in their ability to produce cytokines [75, 76]. Aging is also associated with increase in levels of proinflammatory cytokines, which consequently leads to an increased inflammatory state [75]. Specifically, in postmenopausal women, there are higher levels of serum proinflammatory cytokines, such as monocyte chemoattractant protein 1 (MCP1/CCL2), tumor necrosis factor alpha (TNFα), and IL-6 and free radicals [59]. On the other hand, CD4+ T and B lymphocytes and cytotoxic activity of NK cells typically decrease [59] (Table 1).

↓ levels of sex steroid hormones lead to
A. ↑ general inflammation
(i) ↑ levels of proinflammatory cytokines MCP1, TNFα, and IL-6
(ii) ↓TLR
B. ↓ decreased immune response
(i) ↑ susceptibility to infections and malignancies
(ii) ↓ response to vaccination
(iii) ↓ decreased CD4 : CD8 ratio
(iv) ↑ number of differentiated memory cells and effector T cells
(v) ↓ frequency of B cells
(vi) ↑ NK but with low cytotoxicity and ability to produce cytokines
(vii) ↓ antimicrobial peptides
(viii) ↓ cervical mucus
(ix) ↓ senescence of immune cells
(x) ↑ loss of DC in the cervix
(xi) ↑ loss of resident memory T cells

A plethora of immune factors, dependent on estrogen, are downregulated during menopause. These include loss of toll-like receptor (TLR) function, decreased secretory antimicrobial components, lack of cervical mucus production, alterations in commensal lactobacilli and acidity of vaginal microenvironment [75], and a general senescence of immune cells [77]. Specific changes in the cervix associated with senescence of immune cells include loss of dendritic cells and resident memory T cells [77]. Further investigation is needed to evaluate the immune response of postmenopausal woman in the cervix.

5. Conclusions

The cervix plays a complex balancing act in female reproduction under the influence of sex steroid hormones, by acting as the pathogen and germ/fetal “gatekeeper,” i.e., on the one hand it blocks ascension of pathogens to the upper FRT, while allowing that of the sperm and elimination of menstrual fluid and fetal passage at birth. Dysfunction of this complex role could lead to serious gynecological and obstetrical complications, such as development of polyps and cysts, dysplasia, cancer and cervical incompetence, urinary tract infections, bacterial vaginosis, candidiasis, and viral infections. Development of effective therapies to these disorders will depend on a comprehensive understanding of the underlying molecular mechanisms governing the immune response of local mucosal and immune cells during the different female reproductive phases. New technologies, such as metagenomics, metabolomics, and transcriptomics, should help delineate these complexities.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.


  1. I. A. Bekhtereva and A. E. Dorosevich, “Histophysiology of epithelial and connective tissue components of the vaginal portion of the uterine cervix,” Morfologiia, vol. 136, no. 5, pp. 90–96, 2009. View at: Google Scholar
  2. M. E. Perez-Muñoz, M.-C. Arrieta, A. E. Ramer-Tait, and J. Walter, “A critical assessment of the “sterile womb” and “in utero colonization” hypotheses: implications for research on the pioneer infant microbiome,” Microbiome, vol. 5, no. 1, p. 48, 2017. View at: Publisher Site | Google Scholar
  3. S. K. Lee, C. J. Kim, D. J. Kim, and J. H. Kang, “Immune cells in the female reproductive tract,” Immune Network, vol. 15, no. 1, pp. 16–26, 2015. View at: Publisher Site | Google Scholar
  4. C. R. Wira, M. Rodriguez-Garcia, and M. V. Patel, “The role of sex hormones in immune protection of the female reproductive tract,” Nature Reviews Immunology, vol. 15, no. 4, pp. 217–230, 2015. View at: Publisher Site | Google Scholar
  5. J. A. Younes, E. Lievens, R. Hummelen, R. van der Westen, G. Reid, and M. I. Petrova, “Women and their microbes: the unexpected friendship,” Trends in Microbiology, vol. 26, no. 1, pp. 16–32, 2018. View at: Publisher Site | Google Scholar
  6. P. Vassilakos, R. Negulescu, and R. Pinto Catarino, “Module 1: anatomy of the cervix, squamocolumnar junction, metaplastic change and transformation zone [module],” September 2017, View at: Google Scholar
  7. W. Prendiville and R. Sankaranarayanan, Anatomy of the Uterine Cervix and the Transformation Zone Colposcopy and Treatment of Cervical Precancer, France International Agency for Research on Cancer, 2017.
  8. L. Anton, A. DeVine, L. J. Sierra, A. G. Brown, and M. A. Elovitz, “miR-143 and miR-145 disrupt the cervical epithelial barrier through dysregulation of cell adhesion, apoptosis and proliferation,” Scientific Reports, vol. 7, no. 1, article 3020, 2017. View at: Publisher Site | Google Scholar
  9. C. R. Wira, K. S. Grant-Tschudy, and M. A. Crane-Godreau, “Epithelial cells in the female reproductive tract: a central role as sentinels of immune protection,” American Journal of Reproductive Immunology, vol. 53, no. 2, pp. 65–76, 2005. View at: Publisher Site | Google Scholar
  10. J. Z. Zhou, S. S. Way, and K. Chen, “Immunology of uterine and vaginal mucosae: (trends in immunology 39, 302-314, 2018),” Trends in Immunology, vol. 39, no. 4, p. 355, 2018. View at: Publisher Site | Google Scholar
  11. C. T. Capaldo and A. Nusrat, “Cytokine regulation of tight junctions,” Biochimica et Biophysica Acta (BBA) - Biomembranes, vol. 1788, no. 4, pp. 864–871, 2009. View at: Publisher Site | Google Scholar
  12. L. Han, R. Taub, and J. T. Jensen, “Cervical mucus and contraception: what we know and what we don’t,” Contraception, vol. 96, no. 5, pp. 310–321, 2017. View at: Publisher Site | Google Scholar
  13. C. D. Blaskewicz, J. Pudney, and D. J. Anderson, “Structure and function of intercellular junctions in human cervical and vaginal mucosal epithelia,” Biology of Reproduction, vol. 85, no. 1, pp. 97–104, 2011. View at: Publisher Site | Google Scholar
  14. D. K. Hickey, M. V. Patel, J. V. Fahey, and C. R. Wira, “Innate and adaptive immunity at mucosal surfaces of the female reproductive tract: stratification and integration of immune protection against the transmission of sexually transmitted infections,” Journal of Reproductive Immunology, vol. 88, no. 2, pp. 185–194, 2011. View at: Publisher Site | Google Scholar
  15. J. D. Neill, “Knobil and Neill’s Physiology of Reproduction. Volume 1,” in Chapter 9. Oviduct and Endometrium: Cyclic Changes in the Primate Oviduct and Endometrium, pp. 337–382, Elsevier Academic Press, London, UK, 3rd edition, 2006. View at: Google Scholar
  16. S. M. Donnelly, B. T. Nguyen, S. Rhyne, J. Estes, S. Jesmin, and C. N. Mowa, “Vascular endothelial growth factor induces growth of uterine cervix and immune cell recruitment in mice,” The Journal of Endocrinology, vol. 217, no. 1, pp. 83–94, 2013. View at: Publisher Site | Google Scholar
  17. K. S. Grant-Tschudy and C. R. Wira, “Paracrine mediators of mouse uterine epithelial cell transepithelial resistance in culture,” Journal of Reproductive Immunology, vol. 67, no. 1-2, pp. 1–12, 2005. View at: Publisher Site | Google Scholar
  18. T. Aasen, S. V. Graham, M. Edward, and M. B. Hodgins, “Reduced expression of multiple gap junction proteins is a feature of cervical dysplasia,” Molecular Cancer, vol. 4, no. 1, p. 31, 2005. View at: Publisher Site | Google Scholar
  19. N. S. McNutt, R. A. Hershberg, and R. S. Weinstein, “Further observations on the occurrence of nexuses in benign and malignant human cervical epithelium,” Journal of Cell Biology, vol. 51, no. 3, pp. 805–825, 1971. View at: Publisher Site | Google Scholar
  20. I. K. Gipson, “Mucins of the human endocervix,” Frontiers in Bioscience, vol. 6, no. 3, pp. D1245–D1255, 2001. View at: Publisher Site | Google Scholar
  21. I. K. Gipson, S. Spurr-Michaud, R. Moccia et al., “MUC4 and MUC5B transcripts are the prevalent mucin messenger ribonucleic acids of the human endocervix,” Biology of Reproduction, vol. 60, no. 1, pp. 58–64, 1999. View at: Publisher Site | Google Scholar
  22. W. H. Kutteh, Z. Moldoveanu, and J. Mestecky, “Mucosal immunity in the female reproductive tract: correlation of immunoglobulins, cytokines, and reproductive hormones in human cervical mucus around the time of ovulation,” AIDS Research and Human Retroviruses, vol. 14, Supplement 1, pp. S51–S55, 1998. View at: Google Scholar
  23. W. H. Kutteh, S. J. Prince, K. R. Hammond, C. C. Kutteh, and J. Mestecky, “Variations in immunoglobulins and IgA subclasses of human uterine cervical secretions around the time of ovulation,” Clinical and Experimental Immunology, vol. 104, no. 3, pp. 538–542, 1996. View at: Publisher Site | Google Scholar
  24. H. D. White, K. M. Crassi, A. L. Givan et al., “CD3+ CD8+ CTL activity within the human female reproductive tract: influence of stage of the menstrual cycle and menopause,” The Journal of Immunology, vol. 158, no. 6, pp. 3017–3027, 1997. View at: Google Scholar
  25. C. M. Boomsma, A. Kavelaars, M. J. Eijkemans et al., “Cytokine profiling in endometrial secretions: a non-invasive window on endometrial receptivity,” Reproductive Biomedicine Online, vol. 18, no. 1, pp. 85–94, 2009. View at: Publisher Site | Google Scholar
  26. J. A. Garcia-Velasco and A. Arici, “Chemokines and human reproduction,” Fertility and Sterility, vol. 71, no. 6, pp. 983–993, 1999. View at: Publisher Site | Google Scholar
  27. D. A. Sullivan and C. R. Wira, “Hormonal regulation of immunoglobulins in the rat uterus: uterine response to multiple estradiol treatments,” Endocrinology, vol. 114, no. 2, pp. 650–658, 1984. View at: Publisher Site | Google Scholar
  28. E. L. Parr and M. B. Parr, “Deposition of C3 on bacteria in the mouse uterus after mating,” Journal of Reproductive Immunology, vol. 12, no. 4, pp. 315–319, 1988. View at: Publisher Site | Google Scholar
  29. J. L. Edwards, E. J. Brown, K. A. Ault, and M. A. Apicella, “The role of complement receptor 3 (CR3) in Neisseria gonorrhoeae infection of human cervical epithelia,” Cellular Microbiology, vol. 3, no. 9, pp. 611–622, 2001. View at: Publisher Site | Google Scholar
  30. R. J. Price and B. Boettcher, “The presence of complement in human cervical mucus and its possible relevance to infertility in women with complement-dependent sperm-immobilizing antibodies,” Fertility and Sterility, vol. 32, no. 1, pp. 61–66, 1979. View at: Publisher Site | Google Scholar
  31. O. A. Vanderpuye, C. A. Labarrere, and J. A. McIntyre, “The complement system in human reproduction,” American Journal of Reproductive Immunology, vol. 27, no. 3-4, pp. 145–155, 1992. View at: Publisher Site | Google Scholar
  32. I. A. Rooney, T. J. Oglesby, and J. P. Atkinson, “Complement in human reproduction: activation and control,” Immunologic Research, vol. 12, no. 3, pp. 276–294, 1993. View at: Publisher Site | Google Scholar
  33. C. MacNeill, G. de Guzman, G. E. Sousa et al., “Cyclic changes in the level of the innate immune molecule, surfactant protein-a, and cytokines in vaginal fluid,” American Journal of Reproductive Immunology, vol. 68, no. 3, pp. 244–250, 2012. View at: Publisher Site | Google Scholar
  34. V. D’Argenio, “The Prenatal Microbiome: A New Player for Human Health,” High Throughput, vol. 7, no. 4, pp. 1–10, 2018. View at: Google Scholar
  35. C. R. Wira and R. M. Rossoll, “Antigen-presenting cells in the female reproductive tract: influence of sex hormones on antigen presentation in the vagina,” Immunology, vol. 84, no. 4, pp. 505–508, 1995. View at: Google Scholar
  36. R. W. Chesnut and H. M. Grey, “Antigen presenting cells and mechanisms of antigen presentation,” Critical Reviews in Immunology, vol. 5, no. 3, pp. 263–316, 1985. View at: Google Scholar
  37. P. K. Wallace, G. R. Yeaman, K. Johnson, J. E. Collins, P. M. Guyre, and C. R. Wira, “MHC class II expression and antigen presentation by human endometrial cells,” The Journal of Steroid Biochemistry and Molecular Biology, vol. 76, no. 1-5, pp. 203–211, 2001. View at: Publisher Site | Google Scholar
  38. C. R. Wira and R. M. Rossoll, “Antigen-presenting cells in the female reproductive tract: influence of the estrous cycle on antigen presentation by uterine epithelial and stromal cells,” Endocrinology, vol. 136, no. 10, pp. 4526–4534, 1995. View at: Publisher Site | Google Scholar
  39. C. R. Wira and R. M. Rossoll, “Oestradiol regulation of antigen presentation by uterine stromal cells: role of transforming growth factor-β production by epithelial cells in mediating antigen-presenting cell function,” Immunology, vol. 109, no. 3, pp. 398–406, 2003. View at: Publisher Site | Google Scholar
  40. B. S. Lashkari and D. O. C. Anumba, “Estradiol alters the immune-responsiveness of cervical epithelial cells stimulated with ligands of Toll-like receptors 2 and 4,” PLoS One, vol. 12, no. 3, article e0173646, 2017. View at: Publisher Site | Google Scholar
  41. J. M. Gonzalez, H. Xu, E. Ofori, and M. A. Elovitz, “Toll-like receptors in the uterus, cervix, and placenta: is pregnancy an immunosuppressed state?” American Journal of Obstetrics and Gynecology, vol. 197, no. 3, pp. 296.e1–296.e6, 2007. View at: Publisher Site | Google Scholar
  42. B. S. Lashkari, S. Shahana, and D. O. Anumba, “Toll-like receptor 2 and 4 expression in the pregnant and non-pregnant human uterine cervix,” Journal of Reproductive Immunology, vol. 107, pp. 43–51, 2015. View at: Publisher Site | Google Scholar
  43. L. O. Moreira and D. S. Zamboni, “NOD1 and NOD2 signaling in infection and inflammation,” Frontiers in Immunology, vol. 3, p. 328, 2012. View at: Publisher Site | Google Scholar
  44. Y. M. Loo and M. Gale Jr., “Immune signaling by RIG-I-like receptors,” Immunity, vol. 34, no. 5, pp. 680–692, 2011. View at: Publisher Site | Google Scholar
  45. E. Kaambo, C. Africa, R. Chambuso, and J.-A. S. Passmore, “Vaginal microbiomes associated with aerobic vaginitis and bacterial vaginosis,” Frontiers in Public Health, vol. 6, p. 78, 2018. View at: Publisher Site | Google Scholar
  46. B. Ma, L. J. Forney, and J. Ravel, “Vaginal microbiome: rethinking health and disease,” Annual Review of Microbiology, vol. 66, no. 1, pp. 371–389, 2012. View at: Publisher Site | Google Scholar
  47. R. Rampersaud, T. M. Randis, and A. J. Ratner, “Microbiota of the upper and lower genital tract,” Seminars in Fetal and Neonatal Medicine, vol. 17, no. 1, pp. 51–57, 2012. View at: Publisher Site | Google Scholar
  48. W. Mulu, M. Yimer, Y. Zenebe, and B. Abera, “Common causes of vaginal infections and antibiotic susceptibility of aerobic bacterial isolates in women of reproductive age attending at Felegehiwot Referral Hospital, Ethiopia: a cross sectional study,” BMC Women's Health, vol. 15, no. 1, p. 42, 2015. View at: Publisher Site | Google Scholar
  49. J. Ravel, P. Gajer, Z. Abdo et al., “Vaginal microbiome of reproductive-age women,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, Supplement 1, pp. 4680–4687, 2011. View at: Publisher Site | Google Scholar
  50. E. A. Miller, D. E. Beasley, R. R. Dunn, and E. A. Archie, “Lactobacilli dominance and vaginal pH: why is the human vaginal microbiome unique?” Frontiers in Microbiology, vol. 7, p. 1936, 2016. View at: Publisher Site | Google Scholar
  51. S. Borges, J. Silva, and P. Teixeira, “The role of lactobacilli and probiotics in maintaining vaginal health,” Archives of Gynecology and Obstetrics, vol. 289, no. 3, pp. 479–489, 2014. View at: Publisher Site | Google Scholar
  52. M. Ilkit and A. B. Guzel, “The epidemiology, pathogenesis, and diagnosis of vulvovaginal candidosis: a mycological perspective,” Critical Reviews in Microbiology, vol. 37, no. 3, pp. 250–261, 2011. View at: Publisher Site | Google Scholar
  53. P. L. Carr, D. Felsenstein, and R. H. Friedman, “Evaluation and management of vaginitis,” Journal of General Internal Medicine, vol. 13, no. 5, pp. 335–346, 1998. View at: Publisher Site | Google Scholar
  54. P. Nyirjesy, “Vaginitis in the adolescent patient,” Pediatric Clinics of North America, vol. 46, no. 4, pp. 733–745, 1999, xi. View at: Publisher Site | Google Scholar
  55. D. Danielsson, P. K. Teigen, and H. Moi, “The genital econiche: focus on microbiota and bacterial vaginosis,” Annals of the New York Academy of Sciences, vol. 1230, no. 1, pp. 48–58, 2011. View at: Publisher Site | Google Scholar
  56. J. Li, J. McCormick, A. Bocking, and G. Reid, “Importance of vaginal microbes in reproductive health,” Reproductive Sciences, vol. 19, no. 3, pp. 235–242, 2012. View at: Publisher Site | Google Scholar
  57. A. L. Givan, H. D. White, J. E. Stern et al., “Flow cytometric analysis of leukocytes in the human female reproductive tract: comparison of fallopian tube, uterus, cervix, and vagina,” American Journal of Reproductive Immunology, vol. 38, no. 5, pp. 350–359, 1997. View at: Publisher Site | Google Scholar
  58. R. T. Trifonova, J. Lieberman, and D. van Baarle, “Distribution of immune cells in the human cervix and implications for HIV transmission,” American Journal of Reproductive Immunology, vol. 71, no. 3, pp. 252–264, 2014. View at: Publisher Site | Google Scholar
  59. C. Gameiro and F. Romao, “Changes in the immune system during menopause and aging,” Frontiers in Bioscience, vol. E2, no. 4, pp. 1299–1303, 2010. View at: Publisher Site | Google Scholar
  60. J. Pudney, A. J. Quayle, and D. J. Anderson, “Immunological microenvironments in the human vagina and cervix: mediators of cellular immunity are concentrated in the cervical transformation zone,” Biology of Reproduction, vol. 73, no. 6, pp. 1253–1263, 2005. View at: Publisher Site | Google Scholar
  61. A. E. Morelli, G. di Paola, and L. Fainboim, “Density and distribution of Langerhans cells in the human uterine cervix,” Archives of Gynecology and Obstetrics, vol. 252, no. 2, pp. 65–71, 1992. View at: Publisher Site | Google Scholar
  62. S. Rabi, J. Lionel, and I. Indrasingh, “Morphological study of dendritic cells in human cervix by zinc iodide osmium method,” Journal of Clinical and Diagnostic Research, vol. 8, no. 6, pp. Ac01–Ac04, 2014. View at: Publisher Site | Google Scholar
  63. N. Jacobs, I. Renard, W. al-Saleh et al., “Distinct T cell subsets and cytokine production in cultures derived from transformation zone and squamous intraepithelial lesion biopsies of the uterine cervix,” American Journal of Reproductive Immunology, vol. 49, no. 1, pp. 6–13, 2003. View at: Publisher Site | Google Scholar
  64. E. Burghardt and A. G. Ostor, “Site and origin of squamous cervical cancer: a histomorphologic study,” Obstetrics and Gynecology, vol. 62, no. 1, pp. 117–127, 1983. View at: Google Scholar
  65. A. E. King and H. O. D. Critchley, “Oestrogen and progesterone regulation of inflammatory processes in the human endometrium,” The Journal of Steroid Biochemistry and Molecular Biology, vol. 120, no. 2-3, pp. 116–126, 2010. View at: Publisher Site | Google Scholar
  66. O. J. Hall and S. L. Klein, “Progesterone-based compounds affect immune responses and susceptibility to infections at diverse mucosal sites,” Mucosal Immunology, vol. 10, no. 5, pp. 1097–1107, 2017. View at: Publisher Site | Google Scholar
  67. B. G. Reed and B. R. Carr, “The normal menstrual cycle and the control of ovulation,” in Endotext, K. R. Feingold, B. Anawalt, A. Boyce et al., Eds.,, Inc., South Dartmouth, MA, USA, 2000. View at: Google Scholar
  68. I. Medina-Estrada, N. Alva-Murillo, J. E. Lopez-Meza, and A. Ochoa-Zarzosa, “Immunomodulatory effects of 17β-estradiol on epithelial cells during bacterial infections,” Journal of Immunology Research, vol. 2018, Article ID 6098961, 11 pages, 2018. View at: Publisher Site | Google Scholar
  69. U. Shanmugasundaram, J. W. Critchfield, J. Pannell et al., “Phenotype and functionality of CD4+ and CD8+ T cells in the upper reproductive tract of healthy premenopausal women,” American Journal of Reproductive Immunology, vol. 71, no. 2, pp. 95–108, 2014. View at: Publisher Site | Google Scholar
  70. G. R. Yeaman, P. M. Guyre, M. W. Fanger et al., “Unique CD8+ T cell-rich lymphoid aggregates in human uterine endometrium,” Journal of Leukocyte Biology, vol. 61, no. 4, pp. 427–435, 1997. View at: Publisher Site | Google Scholar
  71. J. Evans and L. A. Salamonsen, “Inflammation, leukocytes and menstruation,” Reviews in Endocrine and Metabolic Disorders, vol. 13, no. 4, pp. 277–288, 2012. View at: Publisher Site | Google Scholar
  72. I. Manaster, S. Mizrahi, D. Goldman-Wohl et al., “Endometrial NK cells are special immature cells that await pregnancy,” Journal of Immunology, vol. 181, no. 3, pp. 1869–1876, 2008. View at: Publisher Site | Google Scholar
  73. L. Schulke, F. Manconi, R. Markham, and I. S. Fraser, “Endometrial dendritic cell populations during the normal menstrual cycle,” Human Reproduction, vol. 23, no. 7, pp. 1574–1580, 2008. View at: Publisher Site | Google Scholar
  74. K. Peacock and K. M. Ketvertis, Menopause. StatPearls, StatPearls Publishing StatPearls Publishing LLC, Treasure Island, FL, USA, 2018.
  75. M. Ghosh, M. Rodriguez-Garcia, and C. R. Wira, “The immune system in menopause: pros and cons of hormone therapy,” The Journal of Steroid Biochemistry and Molecular Biology, vol. 142, pp. 171–175, 2014. View at: Publisher Site | Google Scholar
  76. R. Solana, R. Tarazona, I. Gayoso, O. Lesur, G. Dupuis, and T. Fulop, “Innate immunosenescence: effect of aging on cells and receptors of the innate immune system in humans,” Seminars in Immunology, vol. 24, no. 5, pp. 331–341, 2012. View at: Publisher Site | Google Scholar
  77. M. Rodriguez-Garcia, J. M. Fortier, F. D. Barr, and C. R. Wira, “Aging impacts CD103+ CD8+ T cell presence and induction by dendritic cells in the genital tract,” Aging Cell, vol. 17, no. 3, article e12733, 2018. View at: Publisher Site | Google Scholar

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