SP and Uterine Immunity: A Timing-Based Perspective on Implantation and Reproductive Success: A narrative review
Keywords:
Embryo Implantation, Endometrium/immunology, Inflammation, Reproductive Techniques, Assisted, SP, Uterus/immunologyAbstract
Seminal plasma plays a multifaceted role in reproduction, extending beyond sperm transport to the modulation of female reproductive tract immunity. Rich in prostaglandins, cytokines, and extracellular vesicles, SP influences endometrial receptivity, embryo implantation, and the immunological dialogue that sustains early pregnancy. This narrative review synthesizes current evidence on the dual actions of SP, supportive and disruptive, on implantation and pregnancy outcomes, with emphasis on the timing of exposure and its implications for reproductive success. A structured literature search of PubMed, Scopus, SCIENCEDIRECT and Web of Science (1990–2025) identified mechanistic, animal, and human studies exploring SP-mediated immune signaling, endometrial response, and implantation outcomes. SP can promote regulatory immune adaptation, angiogenesis, and trophoblast invasion that favor implantation. However, exposure outside the receptive window or under inflammatory conditions may trigger pathological cytokine activation linked to implantation failure, PE, and other gestational complications. Evidence from human and animal models highlights the importance of temporally
controlled SP exposure. In assisted reproduction (ART), where natural SP contact is absent, these mechanisms offer translational insight for improving uterine receptivity. The impact of SP on implantation depends critically on timing and maternal immune context. Understanding this balance may guide novel strategies to enhance natural and assisted conception outcomes while minimizing inflammation-associated complications.
Downloads
References
1. Adefuye, A. O., Adeola, H. A., Sales, K. J., & Katz, A. A. (2016). Seminal Fluid-Mediated Inflammation in Physiology and Pathology of the Female Reproductive Tract. Journal of Immunology Research, 2016, 9707252. https://doi.org/10.1155/2016/9707252
2. Ahmadi, H., Csabai, T., Gorgey, E., Rashidiani, S., Parhizkar, F., & Aghebati-Maleki, L. (2022). Composition and effects of seminal plasma in the female reproductive tracts on implantation of human embryos. Biomedicine & Pharmacotherapy, 151, 113065. https://doi.org/10.1016/j.biopha.2022.113065
3. Aitken, R. J., & Baker, M. A. (2006). Oxidative stress, sperm survival and fertility control. Molecular and Cellular Endocrinology, 250(1–2), 66–69. https://doi.org/10.1016/j.mce.2005.12.026
4. Anamthathmakula, P., Erickson, J. A., & Winuthayanon, W. (2022). Blocking serine protease activity prevents semenogelin degradation leading to hyperviscous semen in humans. Biology of Reproduction, 106(5), 879–887. https://doi.org/10.1093/biolre/ioac023
5. Anamthathmakula, P., & Winuthayanon, W. (2020). Mechanism of semen liquefaction and its potential for a novel non-hormonal contraception†. Biology of Reproduction, 103(2), 411–426. https://doi.org/10.1093/biolre/ioaa075
6. Andrade, G. M., Campos, E. P., Ruiz-Rosado, J. de D., Canseco, E. G. M., Lee, A., & Vasquez-Martinez, G. (2024). Prostaglandins suppress neutrophil function after sexual intercourse and may promote urinary tract infections. Medical Hypotheses, 192, 111481. https://doi.org/10.1016/j.mehy.2024.111481
7. Andrade, G. M., Martínez, G. V., Mayoral, L. P.-C., Hernández-Huerta, M. T., Zenteno, E., Mayoral, E. P.-C., Cruz, M. M., Cruz, R. M., Matias-Cervantes, C. A., Cruz, N. M., Díaz, C. R., Cruz-Parada, E., & Pérez-Campos, E. (2020). Molecules and Prostaglandins Related to Embryo Tolerance. Frontiers in Immunology, 11, 555414. https://doi.org/10.3389/fimmu.2020.555414
8. Aplin, J. D., & Ruane, P. T. (2017). Embryo-epithelium interactions during implantation at a glance. Journal of Cell Science, 130(1), 15–22. https://doi.org/10.1242/jcs.175943
9. Ata, B., Abou-Setta, A. M., Seyhan, A., & Buckett, W. (2018). Application of seminal plasma to female genital tract prior to embryo transfer in assisted reproductive technology cycles (IVF, ICSI and frozen embryo transfer). The Cochrane Database of Systematic Reviews, 2(2), CD011809. https://doi.org/10.1002/14651858.CD011809.pub2
10. Bansal, A., Hadimani, C. P., Patil, S. B., & Lah, N. A. Z. B. N. (2025). Evaluating Asymmetric Dimethylarginine (ADMA) as a Biomarker for Preeclampsia: A Meta-Analysis. Journal of Neonatal Surgery, 14(1S), 758–764. https://doi.org/10.52783/jns.v14.1599
11. Battersby, S., Sales, K. J., Williams, A. R., Anderson, R. A., Gardner, S., & Jabbour, H. N. (2007). Seminal plasma and prostaglandin E2 up-regulate fibroblast growth factor 2 expression in endometrial adenocarcinoma cells via E-series prostanoid-2 receptor-mediated transactivation of the epidermal growth factor receptor and extracellular signal-regulated kinase pathway. Human Reproduction (Oxford, England), 22(1), 36–44. https://doi.org/10.1093/humrep/del328
12. Bromfield, J. J. (2014). Seminal fluid and reproduction: Much more than previously thought. Journal of Assisted Reproduction and Genetics, 31(6), 627–636. https://doi.org/10.1007/s10815-014-0243-y
13. Chan, H. Y., & Robertson, S. A. (2025). Seminal fluid effects on uterine receptivity to embryo implantation: Transcriptomic strategies to define molecular mechanisms. Reproduction, Fertility and Development, 37(6). https://doi.org/10.1071/RD24162
14. Chicea, R., Ispasoiu, F., & Focsa, M. (2013). Seminal plasma insemination during ovum-pickup—A method to increase pregnancy rate in IVF/ICSI procedure. A pilot randomized trial. Journal of Assisted Reproduction and Genetics, 30(4), 569–574. https://doi.org/10.1007/s10815-013-9955-7
15. Cooper, M. D., & Rompalo, A. M. (2013). Chapter 2 - The Genital Tract: Anatomical, Developmental, and Microbiological Factors Affecting Sexually Transmitted Disease Acquisition. In L. R. Stanberry & S. L. Rosenthal (Eds.), Sexually Transmitted Diseases (Second Edition) (pp. 45–70). Academic Press. https://doi.org/10.1016/B978-0-12-391059-2.00002-4
16. Crants, S., Yin, S., Andrusier, M. A., Reddy, R., & Ginsburg, E. S. (2024). The Role of Cytokines in Early Pregnancy: Fertilization, Implantation, and Maintenance. Current Obstetrics and Gynecology Reports, 13(2), 59–65. https://doi.org/10.1007/s13669-024-00380-3
17. Crawford, G., Ray, A., Gudi, A., Shah, A., & Homburg, R. (2015). The role of seminal plasma for improved outcomes during in vitro fertilization treatment: Review of the literature and meta-analysis. Human Reproduction Update, 21(2), 275–284. https://doi.org/10.1093/humupd/dmu052
18. Dekel, N. (2014). The role of inflammation for a successful implantation—PubMed.
19. Dekel, N., Gnainsky, Y., Granot, I., & Mor, G. (2010a). Inflammation and implantation. American Journal of Reproductive Immunology (New York, N.Y.: 1989), 63(1), 17–21. https://doi.org/10.1111/j.1600-0897.2009.00792.x
20. Dekel, N., Gnainsky, Y., Granot, I., & Mor, G. (2010b). Inflammation and implantation. American Journal of Reproductive Immunology (New York, N.Y.: 1989), 63(1), 17–21. https://doi.org/10.1111/j.1600-0897.2009.00792.x
21. Dekel, N., Gnainsky, Y., Granot, I., Racicot, K., & Mor, G. (2014). The role of inflammation for a successful implantation. American Journal of Reproductive Immunology (New York, N.Y.: 1989), 72(2), 141–147. https://doi.org/10.1111/aji.12266
22. Dekker, G. A., Robillard, P. Y., & Hulsey, T. C. (1998). Immune maladaptation in the etiology of preeclampsia: A review of corroborative epidemiologic studies. Obstetrical and Gynecological Survey, 53(6), 377–382. Scopus. https://doi.org/10.1097/00006254-199806000-00023
23. du Fossé, N., Lashley, E., Anholts, J., van Beelen, E., le Cessie, S., van Lith, J., Eikmans, M., & van der Hoorn, M. (2023). POSTER 26Impaired immunomodulatory effects of seminal plasma may contribute to unexplained recurrent pregnancy loss: Results of an in vitro study. Journal of Reproductive Immunology, 158, 103609. https://doi.org/10.1016/j.jri.2022.103609
24. Ferramosca, A., & Zara, V. (2014). Bioenergetics of Mammalian Sperm Capacitation. BioMed Research International, 2014, 902953. https://doi.org/10.1155/2014/902953
25. Glasser, S. R., Julian, J., Munir, M. I., & Soares, M. J. (1987). Biological markers during early pregnancy: Trophoblastic signals of the peri-implantation period. Environmental Health Perspectives, 74, 129–147. https://doi.org/10.1289/ehp.8774129
26. Greenwood, J. D., Minhas, K., di Santo, J. P., Makita, M., Kiso, Y., & Croy, B. A. (2000). Ultrastructural studies of implantation sites from mice deficient in uterine natural killer cells. Placenta, 21(7), 693–702. https://doi.org/10.1053/plac.2000.0556
27. Guimond, M.-J., Luross, J. A., Wang, B., Terhorst, C., Danial, S., & Anne Croy, B. (1997). Absence of Natural Killer Cells during Murine Pregnancy is Associated with Reproductive Compromise in TgE26 Mice1. Biology of Reproduction, 56(1), 169–179. https://doi.org/10.1095/biolreprod56.1.169
28. Guo, Z.-Q., Zhang, D.-D., Pang, L., Wang, Y.-T., Cao, P., & Zhang, S.-L. (2019). Semen affects the biological behavior of HeLa cells by altering ERK signaling. Archives of Medical Science : AMS, 16(4), 915–923. https://doi.org/10.5114/aoms.2019.81738
29. Hanna, J., Goldman-Wohl, D., Hamani, Y., Avraham, I., Greenfield, C., Natanson-Yaron, S., Prus, D., Cohen-Daniel, L., Arnon, T. I., Manaster, I., Gazit, R., Yutkin, V., Benharroch, D., Porgador, A., Keshet, E., Yagel, S., & Mandelboim, O. (2006). Decidual NK cells regulate key developmental processes at the human fetal-maternal interface. Nature Medicine, 12(9), 1065–1074. https://doi.org/10.1038/nm1452
30. Ibrahim, A., Engku Ismail, E. H., Irwan Khoo, M., Yusuf, L., Nik Hussain, N. H., Mat Zin, A. A., Noordin, L., Abdullah, S., Mahdy, Z. A., & Nik Lah, N. A. Z. (2025). Impaired implantation as a major upstream pathway of preeclampsia: A narrative synthesis of mechanistic, epidemiological and biomarker evidence. Frontiers in Reproductive Health, 7, 1743504. https://doi.org/10.3389/frph.2025.1743504
31. Ibrahim, A., Khoo, M. I., Ismail, E. H. E., Hussain, N. H. N., Zin, A. A. M., Noordin, L., Abdullah, S., Mahdy, Z. A., & Lah, N. A. Z. N. (2024). Oxidative stress biomarkers in pregnancy: A systematic review. Reproductive Biology and Endocrinology, 22(1), 93. https://doi.org/10.1186/s12958-024-01259-x
32. Juyena, N. S., & Stelletta, C. (2012). Seminal plasma: An essential attribute to spermatozoa. Journal of Andrology, 33(4), 536–551. https://doi.org/10.2164/jandrol.110.012583
33. K, H., S, T., & A, S. (1991). Importance of Ca2+, K+ and glucose in the medium for sperm penetration through the human zona pellucida. The Tohoku Journal of Experimental Medicine, 165(2). https://doi.org/10.1620/tjem.165.99
34. Le Bouteiller, P., & Piccinni, M.-P. (2008). Human NK cells in pregnant uterus: Why there? American Journal of Reproductive Immunology (New York, N.Y.: 1989), 59(5), 401–406. https://doi.org/10.1111/j.1600-0897.2008.00597.x
35. Luo, M., He, N., Xu, Q., Wen, Z., Wang, Z., Zhao, J., & Liu, Y. (2024). Roles of prostaglandins in immunosuppression. Clinical Immunology (Orlando, Fla.), 265, 110298. https://doi.org/10.1016/j.clim.2024.110298
36. Lyons, H. E., Arman, B. M., Robertson, S. A., & Sharkey, D. J. (2023). Immune regulatory cytokines in seminal plasma of healthy men: A scoping review and analysis of variance. Andrology, 11(7), 1245–1266. https://doi.org/10.1111/andr.13424
37. Mahdy, Z. A., Chin, K.-Y., Nik-Ahmad-Zuky, N. L., Kalok, A., & Abdul Rahman, R. (2022). Tocotrienol in Pre-Eclampsia Prevention: A Mechanistic Analysis in Relation to the Pathophysiological Framework. Cells, 11(4), 614. https://doi.org/10.3390/cells11040614
38. Manjunath, P., Bergeron, A., Lefebvre, J., & Fan, J. (2007). Seminal plasma proteins: Functions and interaction with protective agents during semen preservation. Society of Reproduction and Fertility Supplement, 65, 217–228.
39. Mayoral Andrade, G., Vásquez Martínez, G., Pérez-Campos Mayoral, L., Hernández-Huerta, M. T., Zenteno, E., Pérez-Campos Mayoral, E., Martínez Cruz, M., Martínez Cruz, R., Matias-Cervantes, C. A., Meraz Cruz, N., Romero Díaz, C., Cruz-Parada, E., & Pérez-Campos, E. (2020). Molecules and Prostaglandins Related to Embryo Tolerance. Frontiers in Immunology, 11, 555414. https://doi.org/10.3389/fimmu.2020.555414
40. Moffett-King, A. (2002). Natural killer cells and pregnancy. Nature Reviews Immunology, 2(9), 656–663. Scopus. https://doi.org/10.1038/nri886
41. Mor, G., Cardenas, I., Abrahams, V., & Guller, S. (2011). Inflammation and pregnancy: The role of the immune system at the implantation site. Annals of the New York Academy of Sciences, 1221(1), 80–87. https://doi.org/10.1111/j.1749-6632.2010.05938.x
42. Moreno, I., Capalbo, A., Mas, A., Garrido-Gomez, T., Roson, B., Poli, M., Dimitriadis, E., Santamaria, X., Vilella, F., & Simon, C. (2023). The human periconceptional maternal-embryonic space in health and disease. Physiological Reviews, 103(3), 1965–2038. https://doi.org/10.1152/physrev.00050.2021
43. Nederlof, I., Meuleman, T., van der Hoorn, M. L. P., Claas, F. H. J., & Eikmans, M. (2017). The seed to success: The role of seminal plasma in pregnancy. Journal of Reproductive Immunology, 123, 24–28. Scopus. https://doi.org/10.1016/j.jri.2017.08.008
44. Owen, D. H., & Katz, D. F. (2005). A review of the physical and chemical properties of human semen and the formulation of a semen simulant. Journal of Andrology, 26(4), 459–469. Scopus. https://doi.org/10.2164/jandrol.04104
45. Pantos, K., Grigoriadis, S., Maziotis, E., Pistola, K., Xystra, P., Pantou, A., Kokkali, G., Pappas, A., Lambropoulou, M., Sfakianoudis, K., & Simopoulou, M. (2022). The Role of Interleukins in Recurrent Implantation Failure: A Comprehensive Review of the Literature. International Journal of Molecular Sciences, 23(4), Article 4. https://doi.org/10.3390/ijms23042198
46. Peri-implantation Sexual Abstinence and Early Placental Positioning: A Randomized Controlled Trial of Placental Location and Pregnancy Outcomes | Journal of Neonatal Surgery. (2025). https://www.jneonatalsurg.com/index.php/jns/article/view/9575
47. Perumal, P. (2012). Seminal Plasma Proteins. Nature Precedings, 1–1. https://doi.org/10.1038/npre.2012.7001.1
48. Rajagopalan, S., Bryceson, Y. T., Kuppusamy, S. P., Geraghty, D. E., Meer, A. van der, Joosten, I., & Long, E. O. (2005). Activation of NK Cells by an Endocytosed Receptor for Soluble HLA-G. PLOS Biology, 4(1), e9. https://doi.org/10.1371/journal.pbio.0040009
49. Rätsep, M. T., Felker, A. M., Kay, V. R., Tolusso, L., Hofmann, A. P., & Croy, B. A. (2015). Uterine natural killer cells: Supervisors of vasculature construction in early decidua basalis. Reproduction (Cambridge, England), 149(2), R91-102. https://doi.org/10.1530/REP-14-0271
50. Rees, J. M., Ford, W. C., & Hull, M. G. (1990). Effect of caffeine and of pentoxifylline on the motility and metabolism of human spermatozoa. Journal of Reproduction and Fertility, 90(1), 147–156. https://doi.org/10.1530/jrf.0.0900147
51. Ribeiro, J. C., Braga, P. C., Martins, A. D., Silva, B. M., Alves, M. G., & Oliveira, P. F. (2021). Antioxidants present in reproductive tract fluids and their relevance for fertility. Antioxidants, 10(9). Scopus. https://doi.org/10.3390/antiox10091441
52. Rizov, M., Andreeva, P., & Dimova, I. (2017). Molecular regulation and role of angiogenesis in reproduction. Taiwanese Journal of Obstetrics and Gynecology, 56(2), 127–132. https://doi.org/10.1016/j.tjog.2016.06.019
53. Robertson, S. A., Care, A. S., & Moldenhauer, L. M. (2018). Regulatory T cells in embryo implantation and the immune response to pregnancy. The Journal of Clinical Investigation, 128(10), 4224. https://doi.org/10.1172/JCI122182
54. Robertson, S. A., Guerin, L. R., Bromfield, J. J., Branson, K. M., Ahlström, A. C., & Care, A. S. (2009). Seminal Fluid Drives Expansion of the CD4+CD25+ T Regulatory Cell Pool and Induces Tolerance to Paternal Alloantigens in Mice1. Biology of Reproduction, 80(5), 1036–1045. https://doi.org/10.1095/biolreprod.108.074658
55. Rodriguez-Martinez, H., Martinez, E. A., Calvete, J. J., Peña Vega, F. J., & Roca, J. (2021). Seminal Plasma: Relevant for Fertility? International Journal of Molecular Sciences, 22(9), 4368. https://doi.org/10.3390/ijms22094368
56. Sadat, Z., Abedzadeh Kalahroudi, M., & Saberi, F. (2012). The Effect of Short Duration Sperm Exposure on Development of Preeclampsia in Primigravid Women. Iranian Red Crescent Medical Journal, 14(1), 20–24.
57. Saftlas, A. F., Rubenstein, L., Prater, K., Harland, K. K., Field, E., & Triche, E. W. (2014). Cumulative exposure to paternal seminal fluid prior to conception and subsequent risk of preeclampsia. Journal of Reproductive Immunology, 101–102, 104–110. https://doi.org/10.1016/j.jri.2013.07.006
58. Sales, K. J., Katz, A. A., Millar, R. P., & Jabbour, H. N. (2002). Seminal plasma activates cyclooxygenase-2 and prostaglandin E2 receptor expression and signalling in cervical adenocarcinoma cells. Molecular Human Reproduction, 8(12), 1065–1070.
59. Salleh, N. (2014). Diverse Roles of Prostaglandins in Blastocyst Implantation. The Scientific World Journal, 2014, 968141. https://doi.org/10.1155/2014/968141
60. Samuelsson, B. (1963). ISOLATION AND IDENTIFICATION OF PROSTAGLANDINS FROM HUMAN SEMINAL PLASMA. 18. PROSTAGLANDINS AND RELATED FACTORS. The Journal of Biological Chemistry, 238, 3229–3234.
61. Schjenken, J. E., & Robertson, S. A. (2015). Seminal fluid signalling in the female reproductive tract: Implications for reproductive success and offspring health. Advances in Experimental Medicine and Biology, 868, 127–158. Scopus. https://doi.org/10.1007/978-3-319-18881-2_6
62. Sharkey. (2012). TGF-β Mediates Proinflammatory Seminal Fluid Signaling in Human Cervical Epithelial Cells | The Journal of Immunology | American Association of Immunologists. https://journals.aai.org/jimmunol/article/189/2/1024/86615/TGF-Mediates-Proinflammatory-Seminal-Fluid
63. Sharkey, D. J., Tremellen, K. P., Briggs, N. E., Dekker, G. A., & Robertson, S. A. (2017). Seminal plasma pro-inflammatory cytokines interferon-γ (IFNG) and C-X-C motif chemokine ligand 8 (CXCL8) fluctuate over time within men. Human Reproduction, 32(7), 1373–1381. https://doi.org/10.1093/humrep/dex106
64. Sharkey, D. J., Tremellen, K. P., Jasper, M. J., Gemzell-Danielsson, K., & Robertson, S. A. (2012). Seminal fluid induces leukocyte recruitment and cytokine and chemokine mRNA expression in the human cervix after coitus. Journal of Immunology (Baltimore, Md.: 1950), 188(5), 2445–2454. https://doi.org/10.4049/jimmunol.1102736
65. Shen, Q., Wu, X., Chen, J., He, C., Wang, Z., Zhou, B., & Zhang, H. (2023). Immune Regulation of Seminal Plasma on the Endometrial Microenvironment: Physiological and Pathological Conditions. International Journal of Molecular Sciences, 24(19), 14639. https://doi.org/10.3390/ijms241914639
66. Simon, A., & Laufer, N. (2012). Assessment and treatment of repeated implantation failure (RIF). Journal of Assisted Reproduction and Genetics, 29(11), 1227–1239. https://doi.org/10.1007/s10815-012-9861-4
67. Song, Z.-H., Li, Z.-Y., Li, D.-D., Fang, W.-N., Liu, H.-Y., Yang, D.-D., Meng, C.-Y., Yang, Y., & Peng, J.-P. (2016). Seminal plasma induces inflammation in the uterus through the γδ T/IL-17 pathway. Scientific Reports, 6, 25118. https://doi.org/10.1038/srep25118
68. Steiner, A. Z., Pritchard, D. A., Young, S. L., & Herring, A. H. (2014). Peri-implantation Intercourse Lowers Fecundability. Fertility and Sterility, 102(1), 178–182. https://doi.org/10.1016/j.fertnstert.2014.03.017
69. Szczykutowicz, J., Kałuża, A., Kaźmierowska-Niemczuk, M., & Ferens-Sieczkowska, M. (2019). The Potential Role of Seminal Plasma in the Fertilization Outcomes. BioMed Research International, 2019. https://doi.org/10.1155/2019/5397804
70. Talluri, T. R., Mal, G., & Ravi, S. K. (2017). Biochemical components of seminal plasma and their correlation to the fresh seminal characteristics in Marwari stallions and Poitou jacks. Veterinary World, 10(2), 214–220. https://doi.org/10.14202/vetworld.2017.214-220
71. Taylor, N. J. (1982). Investigation of sperm-induced cervical leucocytosis by a double mating study in rabbits. Journal of Reproduction and Fertility, 66(1), 157–160. https://doi.org/10.1530/jrf.0.0660157
72. Templeton, A. A., Cooper, I., & Kelly, R. W. (1978). Prostaglandin concentrations in the semen of fertile men. Journal of Reproduction and Fertility, 52(1), 147–150. https://doi.org/10.1530/jrf.0.0520147
73. Turunen, T., Magris, M., Malinen, M., & Kekäläinen, J. (2022). Seminal-Plasma-Mediated Effects on Sperm Performance in Humans. Cells, 11(14), 2147. https://doi.org/10.3390/cells11142147
74. van den Berg, J. S., Molina, N. M., Altmäe, S., Arends, B., & Steba, G. S. (2024). A systematic review identifying seminal plasma biomarkers and their predictive ability on IVF and ICSI outcomes. Reproductive BioMedicine Online, 48(2), 103622. https://doi.org/10.1016/j.rbmo.2023.103622
75. von Wolff, M., Nowak, O., Pinheiro, R. M., & Strowitzki, T. (2007). Seminal plasma—Immunomodulatory potential in men with normal and abnormal sperm count. European Journal of Obstetrics & Gynecology and Reproductive Biology, 134(1), 73–78. https://doi.org/10.1016/j.ejogrb.2007.01.009
76. Wang, F., Qualls, A. E., Marques-Fernandez, L., & Colucci, F. (2021). Biology and pathology of the uterine microenvironment and its natural killer cells. Cellular and Molecular Immunology, 18(9), 2101–2113. https://doi.org/10.1038/s41423-021-00739-z
77. Wang, Y., Fu, X., & Li, H. (2025). Mechanisms of oxidative stress-induced sperm dysfunction. Frontiers in Endocrinology, 16, 1520835. https://doi.org/10.3389/fendo.2025.1520835
78. Wen, B., Liao, H., Lin, W., Li, Z., Ma, X., Xu, Q., & Yu, F. (2023). The Role of TGF-β during Pregnancy and Pregnancy Complications. International Journal of Molecular Sciences, 24(23), Article 23. https://doi.org/10.3390/ijms242316882
79. Williams, A. C., & Ford, W. C. L. (2001). The Role of Glucose in Supporting Motility and Capacitation in Human Spermatozoa. Journal of Andrology, 22(4), 680–695. https://doi.org/10.1002/j.1939-4640.2001.tb02229.x
80. Yanaihara, A., Iwasaki, S., & Okai, T. (2005). Causes and Treatment of Implantation Failure. Taiwanese Journal of Obstetrics and Gynecology, 44(1), 26–30. https://doi.org/10.1016/S1028-4559(09)60102-9
81. Zhou, J., West, R. C., Ehlers, E. L., Ezashi, T., Schulz, L. C., Roberts, R. M., Yuan, Y., & Schust, D. J. (2021). Modeling human peri-implantation placental development and function†. Biology of Reproduction, 105(1), 40–51. https://doi.org/10.1093/biolre/ioab080.
Downloads
Published
How to Cite
Issue
Section
License

This work is licensed under a Creative Commons Attribution 4.0 International License.
You are free to:
- Share — copy and redistribute the material in any medium or format
- Adapt — remix, transform, and build upon the material for any purpose, even commercially.
Terms:
- Attribution — You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
- No additional restrictions — You may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.