Immune-Endocrine Cross-Talk in Reproductive Biology and PathologyView this Special Issue
Review Article | Open Access
Anna Rapacz-Leonard, Małgorzata Dąbrowska, Tomasz Janowski, "Major Histocompatibility Complex I Mediates Immunological Tolerance of the Trophoblast during Pregnancy and May Mediate Rejection during Parturition", Mediators of Inflammation, vol. 2014, Article ID 579279, 11 pages, 2014. https://doi.org/10.1155/2014/579279
Major Histocompatibility Complex I Mediates Immunological Tolerance of the Trophoblast during Pregnancy and May Mediate Rejection during Parturition
During pregnancy in larger mammals, the maternal immune system must tolerate the fetus for months while resisting external infection. This tolerance is facilitated by immunological communication between the fetus and the mother, which is mediated by Major Histocompatibility Complex I (MHC I) proteins, by leukocytes, and by the cytokines secreted by the leukocytes. Fetal-maternal immunological communication also supports pregnancy by inducing physiological changes in the mother. If the mother “misunderstands” the signal sent by the fetus during pregnancy, the fetus will be miscarried or delivered preterm. Unlike any other maternal organ, the placenta can express paternal antigens. At parturition, paternal antigens are known to be expressed in cows and may be expressed in horses, possibly so that the maternal immune system will reject the placenta and help to expel it. This review compares fetal-maternal crosstalk that is mediated by the immune system in three species with pregnancies that last for nine months or longer: humans, cattle, and horses. It raises the possibility that immunological communication early in pregnancy may prepare the mother for successful expulsion of fetal membranes at parturition.
During pregnancy in larger mammals, the maternal immune system must tolerate the fetus for months. Although in mice tolerance is accomplished by suppression of maternal immune cells, species with longer pregnancies probably cannot suppress their immune systems to the same extent because this would make them prone to infections .
To examine how the immunological challenge of a long gestation period is met, we chose three well-studied species with pregnancies that last nine months or longer: humans, cattle, and horses. In these species, tolerance is mediated by Major Histocompatibility Complex proteins, by leukocytes, and by the cytokines secreted by the leukocytes . If the mother “misunderstands” the signal sent by the fetus during pregnancy, the fetus will be miscarried or delivered preterm . Interestingly, although it might be assumed that tolerance would be accomplished in all these species by “hiding” the fetus from the maternal immune system, paternally inherited antigens are expressed during early pregnancy by trophoblast cells in cattle and horses. At parturition, paternal antigens are known to be expressed in cows, possibly so that the maternal immune system will reject the placenta and help to expel it [4, 5].
This review compares fetal-maternal crosstalk that is mediated by the immune system in humans, cattle, and horses. It examines physiological pregnancy (in which gestation is not shortened and the fetus is not miscarried or delivered preterm), pathological pregnancy, and parturition. It suggests the hypothesis that, in horses and cows, the expression of paternal antigens by invading trophoblast cells may educate the maternal immune system and prepare it for rapid rejection of fetal membranes at parturition.
2. Major Histocompatibility Complex Class I (MHC I)
2.1. MHC I Proteins Mediate Communication between the Fetus and the Mother
There are two classes of MHC I: classical and nonclassical (Table 1). Classical MHC are highly polymorphic, which means they have the ability to present many antigens including foreign antigens . If cells express these foreign antigens they are attacked by cytotoxic T lymphocytes (CTL) .
Nonclassical MHC I are not polymorphic and present a so-called “zero” antigen. The “zero” antigen fills a groove in nonclassical MHC I proteins and is recognized by leukocytes as a maternal “self” antigen; however, it is not of maternal origin. The cells that express “zero” antigen are protected because cells that do not express any antigen are attacked by uterine Natural Killer cells (uNK) [8, 9].
Communication between MHC I and leukocytes (uterine Natural Killer cells, macrophages, and T lymphocytes) induces and maintains maternal tolerance during physiological pregnancy. In humans, cattle, and horses, expression of MHC I is increased by trophoblast cells that invade the endometrium as they become more exposed to the maternal immune system .
The pattern of expression of MHC I differs according to the species. In humans, the trophoblast expresses nonclassical MHC I. These nonclassical MHC I bind a “zero” antigen that protects the cells by binding with uNK [8, 9]. In cattle and horses, the invasive trophoblast expresses classical MHC I with paternal antigens [10, 11], and this pattern of expression stimulates a response from cytotoxic T lymphocytes (CTL) [6, 7]. The reasons for different patterns of expression of MHC I on invasive trophoblast are not clear, although this might be associated with the structure of the placenta in different species.
2.2. Humans (Invasive Placenta)
In humans, nonclassical MHC I enters the maternal circulation, which is probably facilitated by the invasive placenta structure (hemochorial placenta) that has been found in this species, as well as in apes, monkeys, and rodents . In these species with invasive placentas, a part of the trophoblast that is called the extravillous trophoblast destroys 3 layers of endometrial tissue so that it can be in direct contact with maternal blood. The blood passes through a disk-shaped zone, which maternal arteries and veins access from the endometrium. Nourishment is passed to the fetus through 3 layers of cells in highly vascularized villi that sink into this disk and are washed by maternal blood . To ensure that enough blood can circulate through this disk, blood pressure in the maternal arteries is increased by a process called spiral artery remodeling [8, 9, 14].
The structure and expression of the MHC I that mediate tolerance and support of pregnancy have been best defined in humans, in which MHC I are referred to as Human Leukocyte Antigen (HLA) (Table 1). Human classical MHC I are polymorphic and are known to exist in several classes . Of these classes, only HLA-C bind “zero” antigens. HLA-C is expressed on the entire surface of the trophoblast villi (Figure 1) . When HLA-C is bound by the KIR2D receptor on uterine Natural Killer cells (uNK), this leads to optimum blood supply to the trophoblast, thus supporting the fetus .
The nonclassical MHC I are not polymorphic, and “zero” antigens are expressed by all 3 known classes: HLA-E, HLA-F, and HLA-G [17–19]. These HLA are soluble and are expressed on the whole surface of the trophoblast villi (the villous and extravillous trophoblast) (Figure 1). Nonclassical HLA mediate both tolerance and support of pregnancy [1, 18–23].
Tolerance is induced by HLA-G, which is known to enter the maternal circulation and bind with the leukocytes immunoglobulin-like receptors (LIR-1 and LIR-2) on uNK, macrophages, and T lymphocytes. After binding, the leukocytes are inactivated and express more LIR-1 receptors [1, 16, 18–23] (Table 3).
Even in pathological pregnancies, only HLA that induce tolerance have been found, that is, HLA with “zero” antigens. Yang et al.  took samples from the trophoblast during pregnancy and cultured them with INF-gamma, a strong proinflammatory cytokine. Normally, when tissues are treated with this cytokine, they respond by expressing HLA-A and HLA-B. These are classical MHC I that induce inflammation and their expression of immune rejection might lead to recognition by cytotoxic T lymphocytes and immune rejection. However, the cultured trophoblast cells in this experiment continued to express only tolerance-inducing HLA-G. This suggests that the mechanisms that lead to expression of only HLA with “zero” antigen during pregnancy are extremely robust, although they remain unknown.
2.3. Cows (Noninvasive Placenta)
Ruminants are known to have noninvasive placentas ; of these species, cows have been studied the most. In noninvasive placentas, the trophoblast has no contact with maternal blood. Instead, nourishment is passed from the mother to the fetus through structures called placentomes . In cows, there are 70–120 placentomes scattered throughout the entire placenta . Placentomes consist of vascularized villi that originate in the trophoblast and the corresponding endometrial crypts into which the villi fit. Nourishment passes from the maternal to the fetal blood through six layers of cells, three in the endometrium and three in the trophoblast villi .
In cows, MHC I are referred to as Bovine Leukocyte Antigen (BoLA) (Table 1). Unlike in humans, classical BoLA with paternal antigens are known to be expressed during physiological pregnancy, in addition to nonclassical BoLA with “zero” antigens [36–38]. Throughout all of pregnancy, the paternal antigens are expressed on binuclear cells, which have a role in supporting pregnancy. Binuclear cells originate in the trophoblast, although the exact details of their origin are unknown. The cells migrate from the trophoblast and invade the endometrium, where they fuse with endometrial cells to create giant trinuclear cells. These giant cells lose the paternal antigens and express no BoLA at all (Figure 2) [10, 36]. Giant cells help to stabilize pregnancy by secreting bovine placenta lactogen, which influences ovarian and placental steroidogenesis and alters maternal metabolism to support fetal growth and development .
In cows, nonclassical BoLA bind “zero” antigens, and they may have a role in inducing tolerance. Unlike humans, these nonclassical BoLA have not been found on the entire surface of the trophoblast but only on the regions between the placentomes (interplacentomal region) and between the villi (arcade region) . Moreover, these BoLA have only been found during the last trimester of pregnancy, not throughout the entire pregnancy as in humans [2, 10]. Nonclassical BoLA are produced in both nonsoluble and soluble forms , so it can be speculated that the soluble BoLA also bind LIR-1 receptors on leukocytes in cows, which could inhibit the leukocytes, similar to as in humans.
During clone pregnancies in cows, classical BoLA with paternal antigens have been found on the trophoblast surface during the first month of pregnancy . It is speculated that this presentation of paternal antigens is connected with the high number of clone pregnancies that are lost due to attack by activated cytotoxic T lymphocytes (CTL) [37, 40]. It is not known why paternal antigens are only presented on the trophoblast in these pregnancies, but it is likely that this is due to altered gene expression caused by the nuclear transfer process .
2.3.1. Parturition in Cows
Although little is known about immunological activity at the time of parturition, research in cows suggests that expulsion of fetal membranes is promoted when the maternal immune system rejects paternal antigens that are presented by the fetal membranes [4, 5]. Classical BoLA with paternal antigens have been found to be expressed by cows at parturition [41–43]. This expression is probably necessary for placenta maturation. The trophoblast villi are the contact zone in the placentomes, and, up to one month before parturition, the endometrial epithelium undergoes a thinning process and then disappears completely. This histological change leads to loosening of the contact area, so that the trophoblast epithelium contacts the connective tissue of the endometrium (the placenta changes from epitheliochorial to synepitheliochorial) [44, 45].
In addition, when paternal antigens are presented by classical BoLA protein on the surface of chorion cells , the antigens are recognized by T lymphocytes (CD 8+). This recognition can be seen as an increased migration of these lymphocytes to the placenta surface. The increased chemotactic activity of the lymphocytes has been well investigated in cows and this activity decreases when cows retain fetal membranes .
In a study by Benedictus et al. , classical BoLA compatibility from the point of view of the immune systems of both the calf and the dam gave a significantly higher risk of retention of fetal membranes with an odds ratio of 16.25. In a study by Streyl et al.  that compared mRNA expression 6 to 26 days before parturition with expression during physiological parturition, upregulation of certain genes during parturition suggested that increased numbers of leukocytes were present in the fetal-maternal contact zones in the placentomes. Nothing further is known about the immunological mechanisms that lead to retention of fetal membranes in cows or in other species. However, it is possible that immunological communication during pregnancy may prepare the cow for rejection and expulsion of fetal membranes at parturition. This possibility is explored in Section 4.
2.4. Horses (“Semi-Invasive” Placenta)
Horses have an epitheliochorial placenta, as do species that are classified as having a noninvasive placenta . However, because the horse placenta has a subpopulation of highly invasive trophoblast cells (called the chorionic girdle), the authors here will refer to this kind of placenta as “semi-invasive.” This subpopulation of invasive cells forms a chorionic girdle that encircles the fetus. By day 35 of pregnancy, cells of the chorionic girdle adhere to the endometrial epithelium and begin to invade the endometrium [49–52] (Figure 3). The aggressive invasive behavior of these cells is similar to the behavior of cells in the human extravillous trophoblast and to metastatic tumor cells . The chorionic girdle disappears at about days 36–38 of pregnancy [50, 54, 55].
Chorionic girdle cells have been found to express MHC I, which is referred to in horses as Equine Leukocyte Antigen (ELA) [49, 56]. This expression quickly diminishes after invasion and is not found in mature endometrial cups [57, 58]. The expression of ELA by other cells during horse pregnancy and at any other time during pregnancy has not been investigated. Moreover, it has not been established whether nonclassical or classical ELA are expressed, nor whether the ELA bind “zero” or paternal antigens. Evidence for the binding of paternal antigens by what would probably be classical ELA is the fact that CD8+ T leukocytes have been found to be attracted to the cells that express ELA . These CD8+ T leukocytes have been found around the chorionic girdle on the same days that MHC I was expressed [11, 30, 51, 56, 57, 59, 60]. Antibodies to paternal antigens that were produced by B lymphocytes have been found at stable levels in the peripheral blood throughout the rest of pregnancy [54, 61–63]. However, CD8+ T leukocytes were not found to attack trophoblast cells that were expressing ELA. This may be because the paternal antigens are expressed for too short a time for the immune system to prepare itself to attack the paternal-antigen presenting cells (the chorionic girdle disappears on days 36–38) [50, 51, 54, 55].
When the chorionic girdle invades the endometrium, it forms distinct nodules in the endometrial stroma. These nodules are called endometrial cups; mature endometrial cups do not express any ELA [57, 58] (Figure 3). Endometrial cups produce equine chorionic gonadotropin (eCG) [64, 65]. eCG stimulates the ovary to produce additional corpus lutea . The corpus lutea secrete a high level of progesterone, which supports the pregnancy . The endometrial cups remain and continue to secrete eCG until about days 90–120, by which time they have degenerated .
The chorionic girdle and the endometrial cups are important for maintaining pregnancy. In donkey-in-horse pregnancies there is no chorionic girdle or endometrial cups, and it has been speculated that this is related to the high rate of abortions in these pregnancies [67, 68].
Cells in the endometrial cups have IL-22R1 receptors which bind IL-22, which is secreted by the chorionic girdle. Binding of Il-22 helps to maintain mucosal immunity, by facilitating endometrial reepithelization and upregulating antimicrobial proteins .
3.1. Leukocytes (uNK, Macrophages, T Lymphocytes) Not Only Tolerate Pregnancy But Also Support It
During pregnancy in all three species described here, maternal leukocytes behave differently in the uterus than they do in the rest of the mother’s body. When uNK from humans , macrophages from humans and cows [69, 70], and T lymphocytes from horses  have been taken from pregnant uteruses and compared to leukocytes taken from the peripheral blood, the uterine leukocytes were found to be inhibited from engaging in normal immune responses, although the mother is able to resist general infection. This phenomenon is known as split immune tolerance .
3.2. Uterine Natural Killer Cells (uNK)
In Humans, Uterine Natural Killer Cells Support the Growth and Development of the Fetal Unit. In humans, uNK cells are the most abundant leukocytes in the placenta (Table 2), and their number remains constant throughout pregnancy . uNK and their receptors are a type of NK cells that are unique to the uterus and they differ structurally from peripheral NK [71, 72]. The phenotype of uNK (, CD16−, and CD3−) distinguishes them from NK in peripheral blood (, , and CD3−) . uNK do not attack the trophoblast; this is mediated by nonclassical MHC I (HLA-G), as mentioned before (Section 2.2).
uNK cells change their structure as pregnancy progresses, and these changes are related to the roles that uNK play in inducing tolerance and support of the fetus and placenta. In the first trimester uNK are granulated . The granules contain angiogenic growth factor and vascular endothelial factor C. Angiogenic growth factor is released when HLA-G binds to the uNK LIR-1 receptor . This growth factor promotes spiral artery remodeling and may increase vascularization in the syncytial villi. Vascular endothelial factor C stimulates the trophoblast to produce TAP-1 protein. This protein induces HLA-G protein loading. This seems to be a feedback loop that helps to stabilize immunological tolerance of the fetus . In the second trimester uNK undergo a degranulation process and in the third trimester only degranulated uNK cells are present in the endometrium . When degranulation starts, uNK stop secreting the above factors and begin to secrete IFN-gamma. This cytokine inhibits the migration of trophoblast cells, protecting the uterus from too much destruction by these invasive cells [7, 31, 75]. Details about what induces uNK cells to change their structure have not been elucidated.
uNK also help support the fetus in other ways. They induce optimal blood supply for the fetus by participating in spiral artery remodeling [8, 9, 14, 16] when their KIR2D receptors bind HLA-C that is present on the surface of the trophoblast. uNK secrete the matrix metalloproteinases MMP2 and MMP9 during implantation on the 8th to 10th day after ovulation . These enzymes break down fibrous proteins that are known as the extracellular matrix. By breaking down this matrix, these metalloproteinases reduce the intercellular gap between the trophoblast and the endometrium . The mechanisms that induce uNK to secrete these metalloproteinases are unknown.
uNK are inhibited from attacking the fetal unit when their LIR-1 receptors bind soluble HLA-G that has entered the maternal circulation (as part of the extravillous trophoblast—Figure 1). This binding also causes the cells to express more inhibitory LIR-1 receptors. In addition, the number of inhibitory LIR-1 receptors increases both on uNK and on macrophages and T leukocytes when the KIR2DL4 receptors on uNK are bound by HLA-G [78–80]. It is not known if and how uNK communicate with the other leukocytes to effect this change in the number of their inhibitory receptors.
The functions of uNK are important for healthy pregnancy in humans. Altered numbers of uNK or decreased numbers of KIR2D receptors on uNK have been associated with fetal growth restriction and insufficient trophoblast invasion , miscarriage [81, 82], implantation failure , and preeclampsia .
So far, uNK have only been found in human pregnancies. Some NK cells have been found in the horse placenta , but none in cows; therefore all the information that we have about the activity of uNK comes from studies with humans.
Macrophages Inhibit the Activity of Other Leukocytes. Information about the activity of uterine macrophages also comes mostly from studies with humans. Macrophages protect pregnancy in humans throughout all of gestation by inhibiting the immune response by uNK, T lymphocytes, and other macrophages . The LIR-1 receptor on macrophages is bound by HLA-G. After this happens, macrophages do not secrete the proinflammatory cytokines TNF-alpha and INF-gamma. Instead they synthesize more LIR-1 receptors and secrete prostaglandin PGE2, which suppresses the activity of other macrophages, T lymphocytes, and uNK [78–80].
CD9 protein is expressed by uterine macrophages; it is bound by pregnancy specific protein (PSG), which is secreted by the trophoblast. After these receptors are bound, the macrophages secrete IL-10, which inhibits secretion of TNF-alpha by uNK and T lymphocytes [85, 86].
To prevent activation of maternal T lymphocytes, macrophages reduce expression of the costimulatory molecules CD80 and CD86 and express indoleamine-2,3-dioxygenase (IDO) [78–80, 86]. IDO is an immunomodulatory enzyme that catalyses degradation of essential L-tryptophan, which inhibits proliferation of T lymphocytes and prevents their activation .
3.4. T Lymphocytes
3.4.1. T Lymphocytes Tolerate the Fetal Unit, and They May Protect It and Support Its Development
Humans. For tolerance of pregnancy, there is a bias toward cytokines production by CD4+ T-helper (TH2) cells and against cytokines production by CD4+ TH1 cells . Naïve CD4+ T lymphocytes recognize HLA-G “zero” antigens (presented on antigen presenting cells) when the antigens bind with their LIR-1 receptors. This recognition inhibits proliferation of CD4+ T-cells, induces their long-term unresponsiveness, and causes differentiation of the CD4+ T-cells into suppressive TH2 cells . Also, secretion of proinflammatory TNF-alpha by CD4+ TH1 cells is inhibited by IL-10 secreted by macrophages .
By avoiding the TH1 response, the fetal unit avoids attack by activated CD8+ cells (CTL). CTL cells are also inhibited when their LIR-1 receptors bind with HLA-G. Moreover, suppressor CD4+ CD25 cells inhibit activation of CTL cells by the same IDO mechanism as macrophages (mentioned in the “Macrophages” section) . However, CD8+ T lymphocytes are present at the site where placenta implantation takes place. These lymphocytes are thought to protect the pregnancy against external antigens and to support trophoblast growth by secreting IL-8, which promotes trophoblast invasion .
Horses. In mares, CD4+ and CD8+ T lymphocytes have been found to cluster around the cells of the invading chorionic girdle, and around the early, mature, and dying endometrial cups (which are formed by the fusion of the girdle cells with endometrial cells) in greater numbers than are found in the rest of the endometrium . As detailed in the section on horse MHC I (ELA), the invading cells express ELA with paternal antigens, but the mature and dying cups do not, and it is unclear how T cells recognize these cells that do not express ELA [57, 58]. It is also unclear why CTL do not destroy the ELA-expressing cells of the invading chorionic girdle and of the early endometrial cup. It appears that both a systemic increase in T-cell tolerance during pregnancy and an unknown inhibitory factor that is produced by trophoblast cells help protect the ELA-expressing cells [55, 90–92].
To mediate tolerance by the maternal immune system during pregnancies in humans, cows, and horses, which normally last for nine months or longer, MHC I present “zero” antigens, which are recognized by leukocytes. These leukocytes secrete cytokines that increase expression of “zero” antigens, further induce tolerance in other leukocytes, and support pregnancy. Although the details of this process are best known in humans, there are findings of immune activity in other species that have not yet been investigated in humans. Much remains to be done both to clarify the mechanisms of maternal immunological tolerance in individual species and to find out which mechanisms are common to all placental mammals and which species are specific. As Bainbridge  points out, the differences between immunological fetal-maternal crosstalk in humans, cattle, and horses may exist because their common ancestor may have had a short gestation period. Thus, these species may have independently evolved different mechanisms to protect the fetus from longer exposure to the maternal immune system.
However, it is interesting to note that, in all three species examined in this review, invasive trophoblast cells increase their expression of MHC I as they become more exposed to the maternal immune system. Bainbridge  has advanced three hypotheses to explain this phenomenon: (1) MHC on trophoblast cells may help them adhere to and invade maternal tissue, (2) MHC expression may protect the invading cell from the maternal immune system, although it is difficult to understand how the paternal antigens on cattle and horse cells would pacify the maternal immune system, and (3) this expression of MHC may protect the entire fetoplacental unit from the maternal immune system, at least in humans, where HLA-G has been found to be able to suppress the proliferation of peripheral blood lymphocytes .
We suggest a fourth hypothesis be added to the three above: in horses and cows, the expression of paternal antigens by invading trophoblast cells may educate the maternal immune system and prepare it for rapid rejection of fetal membranes at parturition (Figure 4). In horses, when trophoblast cells that display paternal antigens invade the endometrium, CD8+ T lymphocytes are attracted to those cells [11, 30, 51, 56, 57, 59]. After this, memory CD8+ T-cells may persist in the mare. This persistence could prepare the immune system for a rapid response to paternal antigens that are presented at or just before parturition, if the unknown factor that inhibited the T-cells is not present in the uterus at parturition. After invasion by chorionic girdle cells, antibodies to paternal antigens that were produced by B lymphocytes have been found to remain at stable levels in the mare’s peripheral blood throughout the rest of pregnancy [52, 61–63]. At parturition, the mare’s immune response to paternal antigens may be similar to what is known to occur in humans when macrophages recognize foreign antigens: the macrophages secrete proinflammatory TNF-alpha and INF-gamma, which activate both other macrophages and T lymphocytes . Similar mechanisms in cows would help explain why classical MHC I compatibility from the point of view of the immune systems of both the calf and the dam gave a significantly higher risk of retention of fetal membranes .
In mammalian species in which pregnancy lasts for months, the maternal immune system must be able to resist infection while tolerating paternal antigens that are expressed by the fetus. Because of the length of pregnancy in these species, simply relying on extensive suppression of the mother’s immune response is probably too risky. Humans, cows, and horses all have gestation periods of nine months or longer, and they have evolved similar mechanisms for meeting this immunological challenge. When MHC I present “zero” antigens, these antigens are recognized by leukocytes, and these leukocytes secrete cytokines which induce tolerance in other leukocytes, stimulate the expression of more “zero” antigens, and help support pregnancy. The details of this process differ between the three species, and much needs to be done to determine which mechanisms are common to all three species, and which are different. In addition, there are reports that suggest that immunological communication may prepare for and promote rapid rejection of fetal membranes during parturition in cows and horses, but whether or how this is done also needs to be determined.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors would like to thank Mark Leonard for help with English grammar and usage.
- D. R. J. Bainbridge, “Evolution of mammalian pregnancy in the presence of the maternal immune system,” Reviews of Reproduction, vol. 5, no. 2, pp. 67–74, 2000.
- C. J. Davies, J. A. Eldridge, P. J. Fisher, and D. H. Schlafer, “Evidence for expression of both classical and non-classical major histocompatibility complex class I genes in bovine trophoblast cells,” American Journal of Reproductive Immunology, vol. 55, no. 3, pp. 188–200, 2006.
- M. R. Peltier, “Immunology of term and preterm labor,” Reproductive Biology and Endocrinology, vol. 1, article 122, 2003, http://www.rbej.com/content/1/1/122.
- C. J. Davies, J. R. Hill, J. L. Edwards et al., “Major histocompatibility antigen expression on the bovine placenta: its relationship to abnormal pregnancies and retained placenta,” Animal Reproduction Science, vol. 82-83, pp. 267–280, 2004.
- I. Joosten, M. F. Sanders, and E. J. Hensen, “Involvement of major histocompatibility complex class I compatibility between dam and calf in the aetiology of bovine retained placenta,” Animal Genetics, vol. 22, no. 6, pp. 455–463, 1991.
- T. Tilburgs, S. A. Scherjon, and F. H. J. Claas, “Major histocompatibility complex (MHC)-mediated immune regulation of decidual leukocytes at the fetal-maternal interface,” Journal of Reproductive Immunology, vol. 85, no. 1, pp. 58–62, 2010.
- J. M. Baker, A. I. Bamford, and D. F. Antczak, “Modulation of allospecific CTL responses during pregnancy in equids: an immunological barrier to interspecies matings?” Journal of Immunology, vol. 162, no. 8, pp. 4496–4501, 1999.
- G. E. Lash and J. N. Bulmer, “Do uterine natural killer (uNK) cells contribute to female reproductive disorders?” Journal of Reproductive Immunology, vol. 88, no. 2, pp. 156–164, 2011.
- G. E. Lash, S. C. Robson, and J. N. Bulmer, “Review: functional role of uterine natural killer (uNK) cells in human early pregnancy decidua,” Placenta, vol. 31, pp. S87–S92, 2010.
- C. J. Davies, P. J. Fisher, and D. H. Schlafer, “Temporal and regional regulation of major histocompatibility complex class I expression at the bovine uterine/placental interface,” Placenta, vol. 21, no. 2-3, pp. 194–202, 2000.
- S. J. Bacon, S. A. Ellis, and D. F. Antczak, “Control of expression of major histocompatibility complex genes in horse trophoblast,” Biology of Reproduction, vol. 66, no. 6, pp. 1612–1620, 2002.
- Comparative Placentation, http://placentation.ucsd.edu/.
- B. M. Carlson, Human Embryology and Developmental Biology, Mosby, 4th edition, 1994.
- A. Robson, L. K. Harris, B. A. Innes et al., “Uterine natural killer cells initiate spiral artery remodeling in human pregnancy,” The FASEB Journal, vol. 26, pp. 4876–4885, 2012.
- A. King, C. Boocock, A. M. Sharkey et al., “Evidence for the expression of HLA-C class I mRNA and protein by human first trimester trophoblast,” Journal of Immunology, vol. 156, no. 6, pp. 2068–2076, 1996.
- J. Trowsdale and A. Moffett, “NK receptor interactions with MHC class I molecules in pregnancy,” Seminars in Immunology, vol. 20, no. 6, pp. 317–320, 2008.
- D. I. Watkins, Z. W. Chen, A. L. Hughes, M. G. Evans, T. F. Tedder, and N. L. Letvin, “Evolution of the MHC class I genes of a New World primate from ancestral homologues of human non-classical genes,” Nature, vol. 346, no. 6279, pp. 60–63, 1990.
- A. Ishitani, N. Sageshima, N. Lee et al., “Protein expression and peptide binding suggest unique and interacting functional roles for HLA-E, F, and G in maternal-placental immune recognition,” Journal of Immunology, vol. 171, no. 3, pp. 1376–1384, 2003.
- T. V. F. Hviid, “HLA-G in human reproduction: aspects of genetics, function and pregnancy complications,” Human Reproduction Update, vol. 12, no. 3, pp. 209–232, 2006.
- J. S. Hunt, M. G. Petroff, P. Morales, P. Sedlmayr, D. E. Geraghty, and C. Ober, “HLA-G in reproduction: studies on the maternal-fetal interface,” Human Immunology, vol. 61, no. 11, pp. 1113–1117, 2000.
- I. Manaster and O. Mandelboim, “The unique properties of human NK cells in the uterine mucosa,” Placenta, vol. 29, pp. S60–S66, 2008.
- F. le Gal, B. Riteau, C. Sedlik et al., “HLA-G-mediated inhibition of antigen-specific cytotoxic T lymphocytes,” International Immunology, vol. 11, no. 8, pp. 1351–1356, 1999.
- B. G. Beinhauer, J. M. McBride, P. Graf et al., “Interleukin 10 regulates cell surface and soluble LIR-2 (CD85d) expression on dendritic cells resulting in T cell hyporesponsiveness in vitro,” European Journal of Immunology, vol. 34, no. 1, pp. 74–80, 2004.
- Y. Yang, W. Chu, D. E. Geraghty, and J. S. Hunt, “Expression of HLA-G in human mononuclear phagocytes and selective induction by IFN-γ,” Journal of Immunology, vol. 156, no. 11, pp. 4224–4231, 1996.
- E. C. Holmes and S. A. Ellis, “Evolutionary history of MHC class I genes in the mammalian order Perissodactyla,” Journal of Molecular Evolution, vol. 49, no. 3, pp. 316–324, 1999.
- R. L. Tallmadge, J. A. Campbell, D. C. Miller, and D. F. Antczak, “Analysis of MHC class i genes across horse MHC haplotypes,” Immunogenetics, vol. 62, no. 3, pp. 159–172, 2010.
- C. Chung, S. R. Leib, D. G. Fraser, S. A. Ellis, and T. C. McGuire, “Novel classical MHC class I alleles identified in horses by sequencing clones of reverse transcription-PCR products,” European Journal of Immunogenetics, vol. 30, no. 6, pp. 387–396, 2003.
- G. F. Codner, M. J. Stear, R. Reeve, L. Matthews, and S. A. Ellis, “Selective forces shaping diversity in the class i region of the major histocompatibility complex in dairy cattle,” Animal Genetics, vol. 43, no. 3, pp. 239–249, 2012.
- G. Grünig, L. Triplett, L. K. Canady, W. R. Allen, and D. F. Antczak, “The maternal leucocyte response to the endometrial cups in horses is correlated with the developmental stages of the invasive trophoblast cells,” Placenta, vol. 16, no. 6, pp. 539–559, 1995.
- A. de Mestre, L. Noronha, B. Wagner, and D. F. Antczak, “Split immunological tolerance to trophoblast,” International Journal of Developmental Biology, vol. 54, no. 2-3, pp. 445–455, 2010.
- J. N. Bulmer, P. J. Williams, and G. E. Lash, “Immune cells in the placental bed,” International Journal of Developmental Biology, vol. 54, no. 2-3, pp. 281–294, 2010.
- T. P. Augustine, “Bovine placenta: a review on morphology, components, and defects from terminology and clinical perspectives,” Theriogenology, vol. 80, pp. 693–705, 2013.
- N. Mansouri-Attia, L. J. Oliveira, N. Forde et al., “Pivotal role for monocytes/macrophages and dendritic cells in maternal immune response to the developing embryo in cattle,” Biology of Reproduction, vol. 87, article 123, 2012.
- G. J. King, Reproduction in Domesticated Animals, Elsevier, Amsterdam, The Netherland, 1993.
- P. L. Senger, Pathways to Pregnancy and Paturition, pp. 306–323, Current Conceptions, 2003.
- D. R. J. Bainbridge, I. L. Sargent, and S. A. Ellis, “Increased expression of major histocompatibility complex (MHC) class I transplantation antigens in bovine trophoblast cells before fusion with maternal cells,” Reproduction, vol. 122, no. 6, pp. 907–913, 2001.
- C. J. Davies, “Why is the fetal allograft not rejected?” Journal of Animal Science, vol. 85, no. 13, pp. E32–35, 2007.
- G. M. O'Gorman, A. Al Naib, S. A. Ellis et al., “Regulation of a bovine nonclassical major histocompatibility complex class I gene promoter,” Biology of Reproduction, vol. 83, no. 2, pp. 296–306, 2010.
- O. V. Patel, M. Hirako, T. Takahashi, N. Sasaki, and I. Domeki, “Plasma bovine placental lactogen concentration throughout pregnancy in the cow; relationship to stage of pregnancy, fetal mass, number and postpartum milk yield,” Domestic Animal Endocrinology, vol. 13, no. 4, pp. 351–359, 1996.
- J. R. Hill, D. H. Schlafer, P. J. Fisher, and C. J. Davies, “Abnormal expression of trophoblast major histocompatibility complex class I antigens in cloned bovine pregnancies is associated with a pronounced endometrial lymphocytic response,” Biology of Reproduction, vol. 67, no. 1, pp. 55–63, 2002.
- S. A. Ellis, I. L. Sargent, B. Charleston, and D. R. J. Bainbridge, “Regulation of MHC class I gene expression is at transcriptional and post-transcriptional level in bovine placental,” Journal of Reproductive Immunology, vol. 37, no. 2, pp. 103–115, 1998.
- M. J. Newman and H. C. Hines, “Production of foetally stimulated lymphocytotoxic antibodies by primiparous cows,” Animal Blood Groups and Biochemical Genetics, vol. 10, no. 2, pp. 87–92, 1979.
- H. C. Hines and M. J. Newman, “Production of foetally stimulated lymphocytotoxic antibodies by multiparous cows,” Animal Blood Groups and Biochemical Genetics, vol. 12, no. 3, pp. 201–206, 1981.
- E. Grünert, Current Therapy in Theriogenology: Etiology and Pathogenesis of Retained Bovine Placenta, Saunders, Philadelphia, Pa, USA, 1986.
- M. Podhalicz-Dziȩgielewska, T. Rotkiewicz, T. Janowski, S. Zduńczyk, and A. Raś, “Histological findings in placentomes of cows with retained placenta,” Medycyna Weterynaryjna, vol. 56, no. 6, pp. 392–394, 2000.
- A. P. Adams, J. G. Oriol, R. E. Campbell, Y. C. Oppenheim, W. R. Allen, and D. F. Antczak, “The effect of skin allografting on the equine endometrial cup reaction,” Theriogenology, vol. 68, no. 2, pp. 237–247, 2007.
- L. Benedictus, A. J. Thomas, R. Jorritsma, C. J. Davies, and A. P. Koets, “Two-way calf to dam major histocompatibility class I compatibility increases risk for retained placenta in cattle,” American Journal of Reproductive Immunology, vol. 67, no. 3, pp. 224–230, 2012.
- D. Streyl, R. Kenngott, N. Herbach et al., “Gene expression profiling of bovine peripartal placentomes: detection of molecular pathways potentially involved in the release of foetal membranes,” Reproduction, vol. 143, no. 1, pp. 85–105, 2012.
- K. E. Vagnoni, B. R. Schram, O. J. Ginther, and D. P. Lunn, “Susceptibility of equine chorionic girdle cells to lymphokine-activated killer cell activity,” American Journal of Reproductive Immunology, vol. 36, no. 3, pp. 184–190, 1996.
- M. M. Brosnahan, D. C. Miller, M. Adams, and D. F. Antczak, “IL-22 is expressed by the invasive trophoblast of the equine (Equus caballus) chorionic girdle,” Journal of Immunology, vol. 188, no. 9, pp. 4181–4187, 2012.
- P. Lunn, K. E. Vagnoni, and O. J. Ginther, “The equine immune response to endometrial cups,” Journal of Reproductive Immunology, vol. 34, no. 3, pp. 203–216, 1997.
- L. E. Noronha and D. F. Antczak, “Maternal immune responses to trophoblast: the contribution of the horse to pregnancy immunology,” American Journal of Reproductive Immunology, vol. 64, no. 4, pp. 231–244, 2010.
- P. Mignatti and D. B. Rifkin, “Biology and biochemistry of proteinases in tumor invasion,” Physiological Reviews, vol. 73, no. 1, pp. 161–195, 1993.
- L. E. Noronha, K. E. Huggler, A. M. de Mestre, D. C. Miller, and D. F. Antczak, “Molecular evidence for natural killer-like cells in equine endometrial cups,” Placenta, vol. 33, no. 5, pp. 379–386, 2012.
- M. J. B. F. Flaminio and D. F. Antczak, “Inhibition of lymphocyte proliferation and activation: a mechanism used by equine invasive trophoblast to escape the maternal immune response,” Placenta, vol. 26, no. 2-3, pp. 148–159, 2005.
- W. L. Donaldson, J. G. Oriol, C. L. Pelkaus, and D. F. Antczak, “Paternal and maternal major histocompatibility complex class I antigens are expressed co-dominantly by equine trophoblast,” Placenta, vol. 15, no. 2, pp. 123–135, 1994.
- J. K. Maher, D. B. Tresnan, S. Deacon, L. Hannah, and D. F. Antczak, “Analysis of MHC class I expression in equine trophoblast cells using in situ hybridization,” Placenta, vol. 17, no. 5-6, pp. 351–359, 1996.
- W. L. Donaldson, J. G. Oriol, A. Plavin, and D. F. Antezak, “Developmental regulation of class I major histocompatibility complex antigen expression by equine trophoblastic cells,” Differentiation, vol. 52, no. 1, pp. 69–78, 1993.
- W. L. Donaldson, C. H. Zhang, J. G. Oriol, and D. F. Antczak, “Invasive equine trophoblast expresses conventional class I Major Histocompatibility Complex antigens,” Development, vol. 110, no. 1, pp. 63–71, 1990.
- A. C. Enders and I. K. Liu, “Lodgement of the equine blastocyst in the uterus from fixation through endometrial cup formation,” Journal of Reproduction and Fertility. Supplement, vol. 44, pp. 427–438, 1991.
- D. F. Antczak, J. M. Miller, and L. H. Remick, “Lymphocyte alloantigens of the horse. II. Antibodies to ELA antigens produced during equine pregnancy,” Journal of Reproductive Immunology, vol. 6, no. 5, pp. 283–297, 1984.
- D. F. Antczak, “Maternal antibody responses in pregnancy,” Current Opinion in Immunology, vol. 1, no. 6, pp. 1135–1140, 1989.
- D. F. Antczak and W. R. Allen, “Maternal immunological recognition of pregnancy in equids,” Journal of Reproduction and Fertility. Supplement, vol. 37, pp. 69–78, 1989.
- W. R. Allen and R. M. Moor, “The origin of the equine endometrial cups. I. Production of PMSG by fetal trophoblast cells,” Journal of Reproduction and Fertility, vol. 29, no. 2, pp. 313–316, 1972.
- K. J. McDowell, M. H. Adams, and C. B. Baker, “Chorionic gonadotropin α and β subunit RNA's are present in equine placental membranes by day 30 of pregnancy,” Journal of Equine Veterinary Science, vol. 13, pp. 515–518, 1993.
- B. D. Murphy, “Equine chorionic gonadotropin: anenigmatic but essential tool,” Animal Reproduction, vol. 9, pp. 223–230, 2012.
- A. C. Enders, S. Meadows, F. Stewart, and W. R. Allen, “Failure of endometrial cup development in the donkey-in-horse model of equine abortion,” Journal of Anatomy, vol. 188, no. 3, pp. 575–589, 1996.
- W. R. Allen, J. H. Kydd, M. S. Boyle, and D. F. Antczak, “Extraspecific donkey-in-horse pregnancy as a model of early fetal death,” Journal of Reproduction and Fertility. Supplement, vol. 35, pp. 197–209, 1987.
- A. Düvell, C. Frank, A. Schnapper, H. J. Schuberth, and A. Sipka, “Classically or alternatively activated bovine monocyte-derived macrophages in vitro do not resemble CD163/Calprotectin biased macrophage populations in the teat,” Innate Immunity, vol. 18, pp. 886–896, 2012.
- J. S. Hunt and S. A. Robertson, “Uterine macrophages and environmental programming for pregnancy success,” Journal of Reproductive Immunology, vol. 32, no. 1, pp. 1–25, 1996.
- H. El Costa, J. Tabiasco, A. Berrebi et al., “Effector functions of human decidual NK cells in healthy early pregnancy are dependent on the specific engagement of natural cytotoxicity receptors,” Journal of Reproductive Immunology, vol. 82, no. 2, pp. 142–147, 2009.
- S. Yagel, “The developmental role of natural killer cells at the fetal-maternal interface,” American Journal of Obstetrics and Gynecology, vol. 201, no. 4, pp. 344–350, 2009.
- M. Shiroishi, K. Tsumoto, K. Amano et al., “Human inhibitory receptors Ig-like transcript 2 (ILT2) and ILT4 compete with CD8 for MHC class I binding and bind preferentially to HLA-G,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 15, pp. 8856–8861, 2003.
- S. S. Kalkunte, T. F. Mselle, W. E. Norris, C. R. Wira, C. L. Sentman, and S. Sharma, “Vascular endothelial growth factor C facilitates immune tolerance and endovascular activity of human uterine NK cells at the maternal-fetal interface,” Journal of Immunology, vol. 182, no. 7, pp. 4085–4092, 2009.
- Y. Hu, J. P. Dutz, C. D. MacCalman, P. Yong, R. Tan, and P. von Dadelszen, “Decidual NK cells alter in vitro first trimester extravillous cytotrophoblast migration: a role for IFN-γ,” Journal of Immunology, vol. 177, no. 12, pp. 8522–8530, 2006.
- A. J. Wilcox, D. D. Baird, and C. R. Weinberg, “Time of implantation of the conceptus and loss of pregnancy,” The New England Journal of Medicine, vol. 340, no. 23, pp. 1796–1799, 1999.
- S. D. Smith, C. E. Dunk, J. D. Aplin, L. K. Harris, and R. L. Jones, “Evidence for immune cell involvement in decidual spiral arteriole remodeling in early human pregnancy,” American Journal of Pathology, vol. 174, no. 5, pp. 1959–1971, 2009.
- K. Cupurdija, D. Azzola, U. Hainz et al., “Macrophages of human first trimester decidua express markers associated to alternative activation,” American Journal of Reproductive Immunology, vol. 51, no. 2, pp. 117–122, 2004.
- M. G. Petroff, P. Sedlmayr, D. Azzola, and J. S. Hunt, “Decidual macrophages are potentially susceptible to inhibition by class Ia and class Ib HLA molecules,” Journal of Reproductive Immunology, vol. 56, no. 1-2, pp. 3–17, 2002.
- J. Heikkinen, M. Möttönen, J. Komi, A. Alanen, and O. Lassila, “Phenotypic characterization of human decidual macrophages,” Clinical and Experimental Immunology, vol. 131, no. 3, pp. 498–505, 2003.
- S. Quenby, M. Bates, T. Doig et al., “Pre-implantation endometrial leukocytes in women with recurrent miscarriage,” Human Reproduction, vol. 14, no. 9, pp. 2386–2391, 1999.
- A. C. Zenclussen, S. Fest, U. Sehmsdorf, E. Hagen, B. F. Klapp, and P. C. Arck, “Upregulation of decidual P-Selectin expression is associated with an increased number of Th1 cell populations in patients suffering from spontaneous abortions,” Cellular Immunology, vol. 213, no. 2, pp. 94–103, 2001.
- E. Tuckerman, N. Mariee, A. Prakash, T. C. Li, and S. Laird, “Uterine natural killer cells in peri-implantation endometrium from women with repeated implantation failure after IVF,” Journal of Reproductive Immunology, vol. 87, no. 1-2, pp. 60–66, 2010.
- P. J. Williams, J. N. Bulmer, R. F. Searle, B. A. Innes, and S. C. Robson, “Altered decidual leucocyte populations in the placental bed in pre-eclampsia and foetal growth restriction: a comparison with late normal pregnancy,” Reproduction, vol. 138, no. 1, pp. 177–184, 2009.
- J. S. Hunt, L. Miller, and J. S. Platt, “Hormonal regulation of uterine macrophages,” Developmental Immunology, vol. 6, no. 1-2, pp. 105–110, 1998.
- M. Mizuno, K. Aoki, and T. Kimbara, “Functions of macrophages in human decidual tissue in early pregnancy,” American Journal of Reproductive Immunology, vol. 31, no. 4, pp. 180–188, 1994.
- D. H. Munn, E. Shafizadeh, J. T. Attwood, I. Bondarev, A. Pashine, and A. L. Mellor, “Inhibition of T cell proliferation by macrophage tryptophan catabolism,” Journal of Experimental Medicine, vol. 189, no. 9, pp. 1363–1372, 1999.
- I. L. Sargent, A. M. Borzychowski, and C. W. G. Redman, “NK cells and human pregnancy: an inflammatory view,” Trends in Immunology, vol. 27, no. 9, pp. 399–404, 2006.
- J. LeMaoult, I. Krawice-Radanne, J. Dausset, and E. D. Carosella, “HLA-G1-expressing antigen-presenting cells induce immunosuppressive CD4+ T cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 18, pp. 7064–7069, 2004.
- A. P. Adams and D. F. Antczak, “Ectopic transplantation of equine invasive trophoblast,” Biology of Reproduction, vol. 64, no. 3, pp. 753–763, 2001.
- D. F. Antczak, “T-cell tolerance to the developing equine conceptus,” Reproduction in Domestic Animals, vol. 47, pp. 376–383, 2012.
- L. E. Noronha and D. F. Antczak, “Modulation of T-cell reactivity during equine pregnancy is antigen Independent,” American Journal of Reproductive Immunology, vol. 68, pp. 107–115, 2012.
- B. Riteau, C. Menier, I. Khalil-Daher et al., “HLA-G inhibits the allogeneic proliferative response,” Journal of Reproductive Immunology, vol. 43, no. 2, pp. 203–211, 1999.
Copyright © 2014 Anna Rapacz-Leonard et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.