Potential role of macrophages as immunoregulators of pregnancy
© Mor and Abrahams; licensee BioMed Central Ltd. 2003
Received: 28 July 2003
Accepted: 02 December 2003
Published: 02 December 2003
The role of the maternal immune system during pregnancy has focused mainly on the aspect of immune tolerance to the invading trophoblast and, therefore, fetus. While this is a critical aspect of reproductive immunology, it is also important to consider the function of the maternal immune system in the promotion of implantation and maintenance of pregnancy. Apoptosis or cell death is not the final stage in tissue development. The quick and effective removal of apoptotic cells by tissue macrophages represents a vital process preventing "leak" of self-antigens and promoting the production of proliferative/survival factors. One of the key requirements of apoptotic cell clearance is the resolution of inflammatory conditions, which, as in the case of pregnancy, may have lethal consequences. This review will focus on decidual macrophages and their role on apoptosis and cell clearance during pregnancy.
The role of the maternal immune system during pregnancy has focused mainly on the aspect of immune tolerance to the invading trophoblast and, therefore, fetus. While this is a critical aspect of reproductive immunology, it is also important to consider the function of the maternal immune system in the promotion of implantation and maintenance of pregnancy. This review will focus on decidual macrophages and their role on apoptosis and cell clearance during pregnancy.
Leucocytes at the implantation site
During normal pregnancy the decidua is populated by a variety of leucocytes , however, cells of the innate immune system seem to dominate this tissue since the levels of lymphocytes are relatively low (1–3%) . At the time of implantation, many of the leucocytes are NK cells, expressing a phenotype distinct from those found in the periphery . As gestation proceeds, NK cell numbers decline and at term these leucocytes are absent . Macrophages constitute 20–30% of the decidual cells at the site of implantation [5, 2, 6, 7] and unlike NK cells, remain high throughout pregnancy [2, 8]. This evidence suggests that the innate immune system is not indifferent to the fetus and may have a role not only in host protection to infections, but also as important players in the feto-maternal immune adjustment. An important aspect in this process is the establishment of an adequate microenvironment that will promote cell grow and will inhibit hazardous inflammatory immune reactions.
Microenvironment of the implantation site
The local environment of the maternal-fetal interface is characterized, not only by the cell types present, but also by the soluble factors produced therein. The production and effects of cytokines at the implantation site is important for the regulation of trophoblast cell grow, differentiation and invasion [9–11]. In normal pregnancies, particularly at the maternal fetal interface, anti-inflammatory, Th-2, cytokines predominate [12, 13] and, therefore, an appropriate balance between pro-inflammatory and anti-inflammatory cytokines is thought to be crucial for determining the success or failure of a pregnancy . It is currently believed that for the continuous normal development of pregnancy, production of inflammatory cytokines such as, inerleukin-2 (IL-2), tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ) is suppressed, whereas production of anti-inflammatory cytokines such as, IL-4, IL-6 or IL-10 is enhanced . Placental and decidual tissues from normal pregnancies have been shown to express both pro- and anti-inflammatory cytokines [14–17]. However, pro-inflammatory, Th-1, cytokines appear to be potentially harmful to pregnancy since excess production of TNF-α or IFN-γ has been associated with pre-term delivery [17–20]. Similarly, low levels of decidual IL-4 and IL-10 have been observed in women suffering from unexplained recurrent abortions and where spontaneous abortion has occurred during the first trimester of pregnancy .
Immune cells, especially the macrophages, are a main source of cytokines and growth factors and contribute to the maintenance of the adequate balance between Th1 and TH2 cytokines at the placental bed.
Apoptosis and implantation
Apoptosis, or programmed cell death, is a natural mechanism by which the body eliminates unnecessary or potentially dangerous cells in order to maintain normal tissue function. During implantation, apoptosis is important for the appropriate tissue remodeling of the maternal decidua and invasion of the developing embryo . Although, first trimester trophoblasts are resistant to Fas-stimulation, apoptosis has been described in the trophoblast layer of placentas from uncomplicated pregnancies throughout gestation, suggesting that there is a constant cell turnover at the site of implantation necessary for the appropriate growth and function of the placenta [21–23]. In addition, the incidence of trophoblast apoptosis is higher in third trimester villi compared to first trimester placenta , suggesting that increasing placental apoptosis may be involved in the process of parturition. In pregnancies complicated by preeclampsia or intrauterine growth restriction (IUGR), there is a greater incidence of placental apoptosis in the first trimester, which is accompanied by insufficient trophoblast invasion [23, 25]. Several mechanisms, in addition to apoptosis, have been described to limit extravillous trophoblast invasion into the uteroplacental arteries. These include reduced expression of integrin α1β1  decreased secretion of metalloproteinase (MMP-9)  and low cell surface plasminogen activator activity, absent expression of vascular endothelial cadherin  and reduced expression of HLA-G . The reduction of these factors, necessary for trophoblast differentiation and invasion is compatible with the hypothesis of increased apoptosis in IUGR because it is known that once the cells, including trophoblast, enter the apoptotic cascade this down regulate their level of transcription . This data suggests that the regulation of placental apoptosis is essential for the normal physiology of pregnancy.
However, cell death by apoptosis is not the end of the story, the clearance of apoptotic bodies represents a critical step in tissue homeostasis, preventing the release of intracellular contents, which may cause tissue damage and the possibility to initiate an inflammatory reaction.
Clearance of apoptotic cells
Different morphological changes accompany the execution of the apoptotic program. Cells first become round and detach from their neighbors. Then, condensation of both the nucleus and cytoplasm occurs without major modification to the other intracellular organelles. Following condensation, nuclear fragmentation and membrane blebbing is observed, resulting in the formation of apoptotic bodies with intact membranes. These morphological changes are a translation of the biochemical modifications, mediated by the activation of the caspase cascade, that are occurring inside of the cell.
Another important cellular change that occurs during apoptosis is the redistribution of membranal proteins, which will allow macrophages to recognize apoptotic cells and direct the phagocytic process. Several receptors have been implicated in the recognition and engulfment of apoptotic cells [30, 31], suggesting that the process of phagocytosis is well regulated and functionally relevant.
Macrophages and clearance of apoptotic cells
The removal of cellular debris, generated as a result of apoptosis, is a challenging task that must be performed to maintain cellular homeostasis. This clearance process, far from being the end, represents an active and coordinate event which sends specific signals to the remaining cells, either for survival or death . The removal of apoptotic bodies is neither a neutral nor a passive process, but rather an active physiological event that may influence not only immune responses, but also the proliferation and differentiation of surrounding cells . Consequently, a signal from a macrophage to the wrong cell type may have profound consequences for the normal physiology of the tissue .
Recent reports have shown that binding to, and ingestion of, apoptotic cells by phagocytes can result in active immunosuppressive and anti-inflammatory responses. Voll et al  found that monocyte secretion of TNFα was inhibited, while production of TGFβ and IL-10 was increased following co-culture of monocytes with apoptotic lymphocytes. Furthermore, in vivo studies have clearly demonstrated that the TGFβ released by macrophages ingesting apoptotic cells, has anti-inflammatory effects in inflamed peritoneum and lungs . Furthermore, the capacity for macrophages to influence cell death may be regulated by the extent of uptake of apoptotic cells . Duffield et al demonstrated that the capacity of macrophages stimulated with IFNγ and LPS or TNFα to induce glomerular cells apoptosis could be suppressed by the uptake of apoptotic cells .
Macrophages at the maternal-fetal interface
Histological analysis of normal placental beds shows the presence of large number of macrophages, which are localized, in the majority of the cases, in the vicinity of apoptotic cells. Indeed, macrophages are one of the major cell types in both the maternal and fetal compartments of the uteroplacental unit . In humans, during the first weeks of implantation, macrophages are found in high numbers in the maternal decidua and in tissues close in proximity to the placenta . Similarly in rodents, macrophages accumulate at or near the implantation site . The dense macrophage-infiltration at the maternal fetal interface suggests that these cells are also involved in specific pregnancy-associated functions, and not only to perform their usual immunological tasks . Hunt and co-workers have implied that maternal macrophages assist in the tissue remodeling necessary to accommodate expansion of extraembryonic tissue . However, macrophages are not merely scavengers of dying cells, but also actively orchestrate apoptosis of unwanted cells during tissue remodeling . Macrophages synthesize and secrete cytokines and growth factors, which govern the local cellular and tissue interactions [39, 42–44]. They also respond to hormonal factors affecting their function and survival [45, 46].
Numerous findings indicate that the capacity for macrophages to influence cell death is regulated by the extent of uptake of apoptotic cells . For example, the cytolysis of tumor cells by activated macrophages is inhibited by the ingestion of apoptotic but not necrotic cells . Similarly, during embryo implantation, uterine epithelial cells surrounding the blastocyst undergo apoptosis and may form an anti-inflammatory environment by increasing Th-2 type cytokines. This may explain the surprising cohabitation of macrophages and trophoblast cells at the implantation site. As stated earlier, the type of cytokines produced by a macrophage depends on its activation state . We propose that during normal pregnancy, the uptake of apoptotic cells suppresses activated macrophages from secreting pro-inflammatory cytokines such as TNF-α and IFN-γ and promotes the release of Th-2 type, anti-inflammatory and immunosuppressive cytokines (Figure 1A). In pregnancies complicated with preeclampsia or IUGR, activated macrophages secrete pro-inflammatory cytokines such as TNF-α and IFN-γ and induce apoptosis in extravillous trophoblast (Figure 1B). This hypothesis is supported by a recent report of Pijnenborg et al  who found a higher incidence of cell clusters secreting TNF-α, probably macrophages, in the placental bed of patients with severe forms of preeclampsia.
Role of apoptotic cell phagocytosis in pregnancy-associated diseases
Apoptosis or cell death is not the final stage in tissue development. The quick and effective removal of apoptotic cells by tissue macrophages represents a vital process preventing "leak" of self-antigens and promoting the production of proliferative/survival factors. One of the key requirements of apoptotic cell clearance is the resolution of inflammatory conditions, which, as in the case of pregnancy, may have lethal consequences. The clearance of the apoptotic trophoblasts at the implantation site by macrophages and its effect on the well being of the placenta throughout pregnancy is a novel area, which warrants investigation. The field of apoptotic cell clearance is beginning to flourish, and many questions remain unanswered.
These studies were supported by grants from the National Institutes of Health: RO1HD37137 and RO1-CA092435-01
- Mincheva-Nilsson L, Baranov V, Yeung M, Hammarstrom S, Hammarstrom ML: Immunomorphologica studies in human decidua-associated lymphoid cells in normal early pregnancy. J Immuno. 1994, 152: 2020-2032.Google Scholar
- Lessin DL, Hunt JS, King CR, Wood GW: Antigen expression by cells near the maternal-fetal interface. Am J Reprod Immunol Microbiol. 1988, 16: 1-7.PubMedGoogle Scholar
- Loke YW, King A: Immunology of implantation. Baillieres Best Pract Res Clin Obstet Gynaecol. 2000, 14: 827-837. 10.1053/beog.2000.0122.View ArticlePubMedGoogle Scholar
- Moffett-King A: Natural killer cells and pregnancy. Nat Rev Immunol. 2002, 2: 656-663. 10.1038/nri886.View ArticlePubMedGoogle Scholar
- Kabawat SE, Mostoufi-Zadeh M, Driscoll SG, Bhan AK: Implantation site in normal pregnancy. A study with monoclonal antibodies. Am J Pathol. 1985, 118: 76-84.PubMed CentralPubMedGoogle Scholar
- Bulmer JN, Pace D, Ritson A: Immunoregulatory cells in human decidua: morphology, immunohistochemistry and function. Reprod Nutr Dev. 1988, 28: 1599-1613.View ArticlePubMedGoogle Scholar
- Uckan D, Steele A, Cherry, Wang BY, Chamizo W, Koutsonikolis A, Gilbert-Barness E, Good RA: Trophoblasts express Fas ligand: a proposed mechanism for immune privilege in placenta and maternal invasion. Mol Hum Reprod. 1997, 3: 655-662. 10.1093/molehr/3.8.655.View ArticlePubMedGoogle Scholar
- Khong TY: Immunohistologic study of the leukocytic infiltrate in maternal uterine tissues in normal and preeclamptic pregnancies at term. Am J Reprod Immunol Microbiol. 1987, 15: 1-8.PubMedGoogle Scholar
- Simon C, Martin JC, Meseguer M, Caballero-Campo P, Valbuena D, Pellicer A: Embryonic regulation of endometrial molecules in human implantation. J Reprod Fertil Suppl. 2000, 55: 43-53.PubMedGoogle Scholar
- Simon C, Moreno C, Remohi J, Pellicer A: Cytokines and embryo implantation. J Reprod Immunol. 1998, 39: 117-131. 10.1016/S0165-0378(98)00017-5.View ArticlePubMedGoogle Scholar
- Formby B: Immunologic response in pregnancy. Its role in endocrine disorders of pregnancy and influence on the course of maternal autoimmune diseases. Endocrinol Metab Clin North Am. 1995, 24: 187-205.PubMedGoogle Scholar
- Wegmann TG, Lin H, Guilbert L, Mosmann TR: Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon?. Immunol Today. 1993, 14: 353-356. 10.1016/0167-5699(93)90235-D.View ArticlePubMedGoogle Scholar
- Aschkenazi S, Naftolin F, Mor G: Menopause, Sex Hormones and the Immune System. Menopause Management. 2000, 9: 6-13.Google Scholar
- Hanna N, Hanna I, Hleb M, Wagner E, Dougherty J, Balkundi D, Padbury J, Sharma S: Gestational age-dependent expression of IL-10 and its receptor in human placental tissues and isolated cytotrophoblasts. J Immunol. 2000, 164: 5721-5728.View ArticlePubMedGoogle Scholar
- Tranchot-Diallo J, Gras G, Parnet-Mathieu F, Benveniste O, Marce D, Roques P, Milliez J, Chaouat G, Dormont D: Modulations of cytokine expression in pregnant women. Am J Reprod Immunol. 1997, 37: 215-226.View ArticlePubMedGoogle Scholar
- von Rango U, Classen-Linke I, Raven G, Bocken F, Beier HM: Cytokine microenvironments in human first trimester decidua are dependent on trophoblast cells. Fertil Steril. 2003, 79: 1176-1186. 10.1016/S0015-0282(02)04829-X.View ArticlePubMedGoogle Scholar
- Bennett WA, Lagoo-Deenadayalan S, Stopple JA, Barber WH, Hale E, Brackin MN, Cowan BD: Cytokine expression by first-trimester human chorionic villi. Am J Reprod Immunol. 1998, 40: 309-318.View ArticlePubMedGoogle Scholar
- Casey ML, Cox SM, Beutler B, Milewich L, MacDonald PC: Cachectin/tumor necrosis factor-alpha formation in human decidua. Potential role of cytokines in infection-induced preterm labor. J Clin Invest. 1989, 83: 430-436.PubMed CentralView ArticlePubMedGoogle Scholar
- Casey ML, Cox SM, Word RA, MacDonald PC: Cytokines and infection-induced preterm labour. Reprod Fertil Dev. 1990, 2: 499-509.View ArticlePubMedGoogle Scholar
- Yoon BH, Romero R, Yang SH, Jun JK, Kim IO, Choi JH, Syn HC: Interleukin-6 concentrations in umbilical cord plasma are elevated in neonates with white matter lesions associated with periventricular leukomalacia. Am J Obstet Gynecol. 1996, 174: 1433-1440.View ArticlePubMedGoogle Scholar
- Levy R, Smith SD, Yusuf K, Huettner PC, Kraus FT, Sadovsky Y, Nelson DM: Trophoblast apoptosis from pregnancies complicated by fetal growth restriction is associated with enhanced p53 expression. Am J Obstet Gynecol. 2002, 186: 1056-1061. 10.1067/mob.2002.122250.View ArticlePubMedGoogle Scholar
- Ratts VS, Tao XJ, Webster CB, Swanson PE, Smith SD, Brownbill P, Krajewski S, Reed JC, Tilly JL, Nelson DM: Expression of BCL-2, BAX and BAK in the trophoblast layer of the term human placenta: a unique model of apoptosis within a syncytium. Placenta. 2000, 21: 361-366. 10.1053/plac.1999.0486.View ArticlePubMedGoogle Scholar
- Smith SC, Baker PN, Symonds EM: Increased placental apoptosis in intrauterine growth restriction. Am J Obstet Gynecol. 1997, 177: 1395-1401.View ArticlePubMedGoogle Scholar
- Smith SC, Baker PN, Symonds EM: Placental apoptosis in normal human pregnancy. Am J Obstet Gynecol. 1997, 177: 57-65.View ArticlePubMedGoogle Scholar
- Allaire AD, Ballenger K, Wells SR, MCMahon MJ, Lessey BA: Placental apoptosis in preeclampsia. Obstetrics and Gynecoly. 2000, 96: 271-276. 10.1016/S0029-7844(00)00895-4.View ArticleGoogle Scholar
- Zhou Y, Damsky CH, Chiu K, Roberts JM, Fisher SJ: Preeclampsia is associated with abnormal expression of adhesion molecules by invasive cytotrophoblasts. J Clin Invest. 1993, 91: 950-960.PubMed CentralView ArticlePubMedGoogle Scholar
- Graham CH, McCrae KR: Altered expression of gelatinase and surface-associated plasminogen activator activity by trophoblast cells isolated from placentas of preeclamptic patients. Am J Obstet Gynecol. 1996, 175: 555-562.View ArticlePubMedGoogle Scholar
- Hara N, Fujii T, Yamashita T, Kozuma S, Okai T, Taketani Y: Altered expression of human leukocyte antigen G (HLA-G) on extravillous trophoblasts in preeclampsia: immunohistological demonstration with anti-HLA-G specific antibody "87G" and anti-cytokeratin antibody "CAM5.2". Am J Reprod Immunol. 1996, 36: 349-358.View ArticlePubMedGoogle Scholar
- Reister F, Frank HG, Heyl W, Kosanke G, Huppertz B, Schroder W, Kaufmann P, Rath W: The distribution of macrophages in spiral arteries of the placental bed in pre-eclampsia differs from that in healthy patients. Placenta. 1999, 20: 229-233. 10.1053/plac.1998.0373.View ArticlePubMedGoogle Scholar
- Fadok VA, Chimini G: The phagocytosis of apoptotic cells. Semin Immunol. 2001, 13: 365-372. 10.1006/smim.2001.0333.View ArticlePubMedGoogle Scholar
- Savill J, Fadok V: Corpse clearance defines the meaning of cell death. Nature. 2000, 407: 784-788. 10.1038/35037722.View ArticlePubMedGoogle Scholar
- Piacentini M, Autuori F: Immunohistochemical localization of tissue transglutaminase and Bcl-2 in rat uterine tissues during embryo implantation and post-partum involution. Differentiation. 1994, 57: 51-61. 10.1046/j.1432-0436.1994.5710051.x.View ArticlePubMedGoogle Scholar
- Duvall E, Wyllie AH, Morris RG: Macrophage recognition of cells undergoing programmed cell death (apoptosis). Immunology. 1985, 56: 351-358.PubMed CentralPubMedGoogle Scholar
- Mor G, Straszewski S, Kamsteeg M: The role of the Fas/FasL system in reproductive organs: Survival and apoptosis. Biochemical Pharmacology. 2002, 64: 1305-1315. 10.1016/S0006-2952(02)01267-4.View ArticlePubMedGoogle Scholar
- Voll RE, Herrmann M, Roth EA, Stach C, Kalden JR, Girkontaite I: Immunosuppressive effects of apoptotic cells. Nature. 1997, 390: 350-351. 10.1038/37022.View ArticlePubMedGoogle Scholar
- Huynh ML, Fadok VA, Henson PM: Phosphatidylserine-dependent ingestion of apoptotic cells promotes TGF-beta1 secretion and the resolution of inflammation. J Clin Invest. 2002, 109: 41-50. 10.1172/JCI200211638.PubMed CentralView ArticlePubMedGoogle Scholar
- Duffield JS, Ware CF, Ryffel B, Savill J: Suppression by apoptotic cells defines tumor necrosis factor-mediated induction of glomerular mesangial cell apoptosis by activated macrophages. Am J Pathol. 2001, 159: 1397-1404.PubMed CentralView ArticlePubMedGoogle Scholar
- De M, Wood GW: Influence of Oestrogen and Progesterone on Macrophage Distribution in the Mouse Uterus. Journal of Endocrinology. 1990, 126: 417-424.View ArticlePubMedGoogle Scholar
- Miller L, Hunt J: Sex steroids hormones and macrophage function. Life Sciences. 1996, 59: 1-14. 10.1016/0024-3205(96)00122-1.View ArticlePubMedGoogle Scholar
- Tachi C, Tachi S: Macrophages and implantation. Ann N Y Acad Sci. 1986, 476: 158-182.View ArticlePubMedGoogle Scholar
- Ben-Hur H, Gurevich P, Berman V, Tchanyshev R, Gurevich E, Zusman I: The secretory immune system as part of the placental barrier in the second trimester of pregnancy in humans. In Vivo. 2001, 15: 429-435.PubMedGoogle Scholar
- Hunt JS: Cytokine networks in the uteroplacental unit: Macrophages as pivotal regulatory cells. Journal of Reproductive Immunology. 1989, 16: 1-17. 10.1016/0165-0378(89)90002-8.View ArticlePubMedGoogle Scholar
- Garcia-Velasco J, Arici A, Naftolin F, Zreick T, Mor G: Macrophage-derived growth factors regulate FasL expression in endometrial stromal cells. Molecular Human Reproduction. 1998, 5: 642-650. 10.1093/molehr/5.7.642.View ArticleGoogle Scholar
- Mor G, Wei Y, Santen R, Gutierrez L, Eliza M, Lev B, Harada N, Wang J, Lysiak J, Diano S, Naftolin F: Macrophages, estrogen and the microenvironment of breast cancer. Journal of Steroid Biochemistry and Molecular Biology. 1998, 67: 403-411. 10.1016/S0960-0760(98)00143-5.View ArticlePubMedGoogle Scholar
- Mor G, Naftolin F: Oestrogen, menopause and the immune system. The Journal of the British Menopause Society. 1998, 4: 4-8.Google Scholar
- Mor G, Sapi E, Abrahams VM, Rutherford T, Song J, Hao XY, Muzaffar S, Kohen F: Interaction of the Estrogen Receptors with the Fas Ligand Promoter in Human Monocytes. J Immunol. 2003, 170: 114-122.View ArticlePubMedGoogle Scholar
- Reiter I, Krammer B, Schwamberger G: Differential effect of apoptotic versus necrotic tumor cells on macrophage antitumor activities. J Immunol. 1999, 163: 1730-1732.PubMedGoogle Scholar
- Cavaillon JM: Cytokines and macrophages. Biomed Pharmacother. 1994, 48: 445-453.View ArticlePubMedGoogle Scholar
- Pijnenborg R, McLaughlin PJ, Vercruysse L, Hanssens M, Johnson PM, Keith J. C., Jr., Van Assche FA: Immunolocalization of tumour necrosis factor-alpha (TNF-alpha) in the placental bed of normotensive and hypertensive human pregnancies. Placenta. 1998, 19: 231-239.View ArticlePubMedGoogle Scholar
- Kim YM, Chaiworapongsa T, Gomez R, Bujold E, Yoon BH, Rotmensch S, Thaler HT, Romero R: Failure of physiologic transformation of the spiral arteries in the placental bed in preterm premature rupture of membranes. Am J Obstet Gynecol. 2002, 187: 1137-1142. 10.1067/mob.2002.127720.View ArticlePubMedGoogle Scholar
- Reister F, Frank HG, Kingdom JC, Heyl W, Kaufmann P, Rath W, Huppertz B: Macrophage-induced apoptosis limits endovascular trophoblast invasion in the uterine wall of preeclamptic women. Lab Invest. 2001, 81: 1143-1152.View ArticlePubMedGoogle Scholar
- Manfredi AA, Rovere P, Galati G, Heltai S, Bozzolo E, Soldini L, Davoust J, Balestrieri G, Tincani A, Sabbadini MG: Apoptotic cell clearance in systemic lupus erythematosus. I. Opsonization by antiphospholipid antibodies. Arthritis Rheum. 1998, 41: 205-214. 10.1002/1529-0131(199802)41:2<205::AID-ART4>3.3.CO;2-S.View ArticlePubMedGoogle Scholar
- Guleria I, Pollard JW: The trophoblast is a component of the innate immune system during pregnancy. Nat Med. 2000, 6: 589-593. 10.1038/75074.View ArticlePubMedGoogle Scholar
- Aschkenazi S, Straszewski S, Verwer KM, Foellmer H, Rutherford T, Mor G: Differential regulation and function of the Fas/Fas ligand system in human trophoblast cells. Biol Reprod. 2002, 66: 1853-1861.View ArticlePubMedGoogle Scholar
- Neale D, Demasio K, Illuzi J, Chaiworapongsa T, Romero R, Mor G: Maternal serum of women with pre-eclampsia reduces trophoblast cell viability: evidence for an increased sensitivity to Fas-mediated apoptosis. J Matern Fetal Neonatal Med. 2003, 13: 39-44.View ArticlePubMedGoogle Scholar
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