Peripheral blood nk cells in patients with uterine scars and abnormally adherent and invasive placenta
- 作者: Ponikarova N.Y.1, Davydova A.A.2, Shelepova E.S.1, Osipova N.A.1, Sokolov D.I.2, Mikhailova V.A.2, Oganyan K.A.2, Selkov S.A.2, Zazerskaya I.E.1
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隶属关系:
- Almazov National Medical Research Centre, Ministry of Health of Russia
- D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
- 期: 编号 1 (2025)
- 页面: 66-72
- 栏目: Original Articles
- URL: https://journals.rcsi.science/0300-9092/article/view/285601
- DOI: https://doi.org/10.18565/aig.2024.303
- ID: 285601
如何引用文章
详细
Objective: The aim of the study was to evaluate cytotoxic activity of peripheral blood NK cells against trophoblast cells in pregnant women with uterine scar and with or without abnormally adherent and invasive placenta (AAIP).
Materials and methods: The study included 18 pregnant women who were divided into 3 groups. The main group (n=6) included women with uterine scar after cesarean section and AAIP. The comparison group (n=6) included women with uterine scar and without AAIP. The control group (n=6) included pregnant women without uterine scar. The women were enrolled in the study at 28–32 weeks of pregnancy. Cytotoxic activity of peripheral blood NK cells against trophoblast cells of the JEG-3 line was evaluated in all patients.
Results: There were no differences in cytotoxic activity of NK cells between the group of women with AAIP and the comparison and control groups. However, the cytotoxic activity of pNK was lower in the group of pregnant women who underwent cesarean section in history versus women with normal pregnancy (p= p=0.022).
Conclusion: The data obtained in this study suggest that reduced cytotoxic activity of pNK cells in women with uterine scar and without AAIP is due to the mechanism that prevents adherence of placenta in a number of patients in risk group.
作者简介
Nataliya Ponikarova
Almazov National Medical Research Centre, Ministry of Health of Russia
编辑信件的主要联系方式.
Email: natalyponi@gmail.com
ORCID iD: 0000-0002-7230-3057
PhD student
俄罗斯联邦, St. PetersburgAlina Davydova
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: alyadavydova@gmail.com
ORCID iD: 0000-0001-5313-2910
Junior Researcher
俄罗斯联邦, St. PetersburgEkatherina Shelepova
Almazov National Medical Research Centre, Ministry of Health of Russia
Email: shelepova_es@almazovcentre.ru
ORCID iD: 0000-0002-3233-8239
PhD, Teaching Assistant
俄罗斯联邦, St. PetersburgNataliya Osipova
Almazov National Medical Research Centre, Ministry of Health of Russia
Email: osipova_na@almazovcentre.ru
Dr. Med. Sci., Professor
俄罗斯联邦, St. PetersburgDmitry Sokolov
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: falcojugger@yandex.ru
ORCID iD: 0000-0002-5749-2531
Dr. Bio. Sci., Professor
俄罗斯联邦, St. PetersburgValentina Mikhailova
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: mva_spb@mail.ru
ORCID iD: 0000-0003-1328-8157
Dr. Bio. Sci., Senior Researcher
俄罗斯联邦, St. PetersburgKarina Oganyan
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: oganyan_karina@bk.ru
ORCID iD: 0000-0002-2743-0882
Resident Physician
俄罗斯联邦, St. PetersburgSergey Selkov
D.O. Ott Research Institute of Obstetrics, Gynecology and Reproductology
Email: selkovsa@mail.ru
ORCID iD: 0000-0003-1560-7529
Merited Scolar of the Russian Federation, Dr. Med. Sci., Professor
俄罗斯联邦, St. PetersburgIrina Zazerskaya
Almazov National Medical Research Centre, Ministry of Health of Russia
Email: zazera@mail.ru
ORCID iD: 0000-0003-4431-3917
Dr. Med. Sci., Professor
俄罗斯联邦, St. Petersburg参考
- Kobayashi H., Matsubara S., Yoshimoto C., Shigetomi H., Imanaka S. Current understanding of the pathogenesis of placenta accreta spectrum disorder with focus on mitochondrial function. J. Obstet. Gynaecol. Res. 2024; 50(6): 929-40. https://dx.doi.org/10.1111/jog.15936.
- Xu X., Zhou Y., Wei H. Roles of HLA-G in the maternal-fetal immune microenvironment. Front. Immunol. 2020; 11: 592010. https://dx.doi.org/ 10.3389/fimmu.2020.592010.
- Kanter J.R., Mani S., Gordon S.M., Mainigi M. Uterine natural killer cell biology and role in early pregnancy establishment and outcomes. F. S. Rev. 2021; 2(4): 265-86. https://dx.doi.org/10.1016/j.xfnr.2021.06.002.
- Gaynor L.M., Colucci F. Uterine natural killer cells: functional distinctions and influence on pregnancy in humans and mice. Front. Immunol. 2017; 8: 467. https://dx.doi.org/10.3389/fimmu.2017.00467.
- El-Badawy O., Helmy A.S., Abbas A.M., Zahran A.M., Afifi N.A., Abdel-Rahim M.H. Concordance between peripheral and decidual NK cell subsets and killer immunoglobulin-like receptors in women with recurrent spontaneous miscarriages. J. Reprod. Immunol. 2020; 140: 103130. https:// dx.doi.org/10.1016/j.jri.2020.103130.
- Chen X., Zhang T., Liu Y., Cheung W.C., Zhao Y., Wang C.C. et al. Uterine CD56+ cell density and euploid miscarriage in women with a history of recurrent miscarriage: A clinical descriptive study. Eur. J. Immunol 2021; 51(2): 487-9. https://dx.doi.org/10.1002/eji.202048868.
- Cooper S., Laird S.M., Mariee N., Li T.C., Metwally M. The effect of prednisolone on endometrial uterine NK cell concentrations and pregnancy outcome in women with reproductive failure. A retrospective cohort study. J. Reprod. Immunol. 2019; 131: 1-6. https://dx.doi.org/10.1016/j.jri.2018.10.001.
- Xie M., Li Y., Meng Y.Z., Xu P., Yang Y.G., Dong S. et al. Uterine natural killer cells: a rising star in human pregnancy regulation. Front. Immunol. 2022; 13: 918550. https://dx.doi.org/10.3389/fimmu.2022.918550.
- Dons'koi B.V., Osypchuk D.V., Chernyshov V.P., Khazhylenko K.G. Expression of natural cytotoxicity receptor NKp46 on peripheral blood natural killer cells in women with a history of recurrent implantation failures. J. Obstet. Gynaecol. Res. 2021; 47(3): 1009-15. https://dx.doi.org/10.1111/jog.14631.
- Deer E., Herrock O., Campbell N., Cornelius D., Fitzgerald S., Amaral L.M. et al. The role of immune cells and mediators in preeclampsia. Nat. Rev. Nephrol. 2023; 19(4): 257-70. https://dx.doi.org/10.1038/s41581-022-00670-0.
- Hecht J.L., Karumanchi S.A., Shainker S.A. Immune cell infiltrate at the utero-placental interface is altered in placenta accreta spectrum disorders. Arch. Gynecol. Obstet. 2020; 301(2): 499-507. https://dx.doi.org/10.1007/ s00404-020-05453-1.
- El-Badawy O., Abbas A.M., Radwan E., Makboul R., Khamis A.A., Ali M. et al. Cross-talk between mucosal-associated invariant T, natural killer, and natural killer T cell populations is implicated in the pathogenesis of placenta accreta spectrum. Inflammation. 2023; 46(4): 1192-208. https://dx.doi.org/10.1007/s10753-023-01799-1.
- AbdelFattah S., Morsy M., Ahmed A.M., Abdelsalam H., Hosny G. Microcellular approach for the pathogenesis of placenta accreta spectrum inflammatory versus apoptotic pathways; a thorough look on Treg, dNK and VEGF. Pathol. Res. Pract. 2024; 254: 155153. https://dx.doi.org/10.1016/j.prp.2024.155153.
- Marron K., Harrity C. Endometrial lymphocyte concentrations in adverse reproductive outcome populations. J. Assist. Reprod. Genet. 2019; 36(5): 837-46. https://dx.doi.org/10.1007/s10815-019-01427-8.
- Министерство здравоохранения Российской Федерации. Клинические рекомендации. Патологическое прикрепление плаценты (предлежание и врастание плаценты). 2023. [Ministry of Health of the Russian Federation. Clinical guidelines. Pathological attachment of the placenta (placenta previa and accreta). 2023. (in Russian)].
- ФГБУ «Северо-Западный федеральный медицинский исследовательский центр имени В.А. Алмазова» Министерства здравоохранения Российской Федерации. Клинические протоколы ведения пациентов по специальности «Акушерство и гинекология». Ч. I. 3-е изд. СПб: Эко-Вектор; 2023. [V.A. Almazov North-Western Federal Medical Research Center of the Ministry of Health of the Russian Federation. Clinical protocols for patient management in the specialty "Obstetrics and Gynecology." Part I. 3rd ed. St. Petersburg: Eco-Vector; 2023. (in Russian)].
- Семенова Е.С., Мащенко И.А., Труфанов Г.Е., Фокин В.А., Ефимцев А.Ю., Лепёхина А.С., Горбунова Е.А., Сергиеня О.В., Шмедык Н.Ю., Тиллоев Т.А. Магнитно-резонансная томография при беременности: актуальные вопросы безопасности. REJR. 2020; 10(1): 216-30. [Semenova E.S., Mashchenko I.A., Trufanov G.E., Fokin V.A., Efimtsev A.Yu., Lepekhina A.S., Gorbunova E.A., Sergienya O.V., Shmedyk N.Yu., Tilloev T.A. Magnetic resonance imaging during pregnancy: current safety issues. REJR. 2020;10(1): 216-30. (in Russian)]. https://dx.doi.org/10.21569/ 2222-7415-2020-10-1-216-230.
- Загайнова В.А., Коган И.Ю., Беспалова О.Н., Сельков С.А., Соколов Д.И. Роль периферических и эндометриальных NK-клеток при повторных репродуктивных потерях. Акушерство и гинекология. 2021; 7: 19-27. [Zagainova V.A., Kogan I.Yu., Bespalova O.N., Selkov S.A., Sokolov D.I. The role of peripheral and endometrial natural killer cells in recurrent reproductive losses. Obstetrics and Gynecology. 2021; (7): 19-27 (in Russian)]. https:// dx.doi.org/10.18565/aig.2021.7.19-27.
- Bulmer J.N., Lash G.E. Uterine natural killer cells: Time for a re-appraisal? F1000Res. 2019; 8: F1000 Faculty Rev-999. https://dx.doi.org/10.12688/f1000research.19132.1.
- Vacca P., Chiossone L., Mingari M.C., Moretta L. Heterogeneity of NK cells and other innate lymphoid cells in human and murine decidua. Front. Immunol. 2019; 10: 170. https://dx.doi.org/10.3389/fimmu.2019.00170.
- Fu B., Wei H. Natural killer cells in reproduction: Before, during and after pregnancy. In: Mor G., ed. Reproductive Immunology: Basic Concepts. 2021: 55-72. https://dx.doi.org/10.1016/B978-0-12-818508-7.00009-9.
- Strunz B., Bister J., Jönsson H., Filipovic I., Crona-Guterstam Y., Kvedaraite E. et al. Continuous human uterine NK cell differentiation in response to endometrial regeneration and pregnancy. Sci. Immunol. 2021; 6(56): eabb7800. https://dx.doi.org/10.1126/sciimmunol.abb7800.
- Михайлова В.А., Давыдова А.А., Загайнова В.А., Сельков С.А., Соколов Д.И. NK-клетки в диагностике репродуктивных нарушений: долгий путь от теории к практике. Тезисы III Общероссийской научно-практической конференции для акушеров-гинекологов «Оттовские чтения». М.: Издательство журнала StatusPraesens; 2021: 18-9. [Mikhailova V.A., Davydova A.A., Zagainova V.A., Selkov S.A., Sokolov D.I. NK cells in the diagnosis of reproductive disorders: a long way from theory to practice. Theses of the III All-Russian Scientific and Practical Conference for Obstetricians and Gynecologists "Ott's Readings". Moscow: StatusPraesens; 2021: 18-9. (in Russian)].
- Toth B., Zhu L., Karakizlis H., Weimer R., Morath C., Opelz G. et al. NK cell subsets in idiopathic recurrent miscarriage and renal transplant patients. J. Reprod. Immunol. 2020; 138: 103098. https://dx.doi.org/10.1016/ j.jri.2020.103098.
- Баженов Д.О., Михайлова В.А. Влияние клеток трофобласта на цитотоксический потенциал NK-клеток. Актуальные проблемы биомедицины - 2021: материалы XXVII Всероссийской конференции молодых ученых с международным участием, Санкт-Петербург, 25-26 марта 2021 года. СПб: Первый Санкт-Петербургский государственный медицинский университет им. академика И.П. Павлова; 2021: 144-5. [Bazhenov D.O., Mikhailova V.A. Effect of trophoblast cells on the cytotoxic potential of NK cells. Topical problems of biomedicine - 2021: materials of the XXVII All-Russian Conference of Young Scientists with International Participation, St. Petersburg, March 25-26, 2021. St. Petersburg: Academician I.P. Pavlov First St. Petersburg State Medical University; 2021: 144-5. (in Russian)].
- Li C., Houser B.L., Nicotra M.L., Strominger J.L. HLA-G homodimer-induced cytokine secretion through HLA-G receptors on human decidual macrophages and natural killer cells. Proc. Natl. Acad. Sci. U. S. A. 2009; 106(14): 5767-72. https://dx.doi.org/10.1073/pnas.0901173106.
- Laban M., Ibrahim E.A., Elsafty M.S., Hassanin A.S. Placenta accreta is associated with decreased decidual natural killer (dNK) cells population: a comparative pilot study. Eur. J. Obstet. Gynecol. Reprod. Biol. 2014; 181: 284-8. https://dx.doi.org/10.1016/j.ejogrb.2014.08.015.
- Skret-Magierlo J., Wicherek L., Basta P., Galazka K., Sikora J., Wilk M. et al. RCAS1 decidual immunoreactivity during cesarean section in scar deciduosis: immune cell presence and activity. Gynecol. Obstet. Invest. 2008; 65(3): 187-94. https://dx.doi.org/10.1159/000111533.
- Smith A.L., Bole Aldo P., Racicot K.E. Placental regulation of immune functions. In: Mor G., ed. Reproductive Immunology: Basic Concepts. 2021: 335-48. https://dx.doi.org/10.1016/B978-0-12-818508-7.00004-X.
- Liu X., Wang Y., Wu Y., Zeng J., Yuan X., Tong C. et al. What we know about placenta accreta spectrum (PAS). Eur. J. Obstet. Gynecol. Reprod. Biol. 2021; 259: 81-9. https://dx.doi.org/10.1016/j.ejogrb.2021.02.001.
- Годзоева А.О., Зазерская И.Е., Васильева Е.Ю., Мащенко И.А., Яковлева Н.Ю., Ли О.А. Прогностическая значимость sFlt-1 и PlGF в диагностике глубокой инвазии плаценты. Журнал акушерства и женских болезней. 2022; 71(2): 39-48. [Godzoeva A.O., Zazerskaya I.E., Vasilyeva E.Y., Mashchenko I.A., Yakovleva N.Y., Li O.A. Prognostic value of sFlt-1 and PlGF in the diagnosis of abnormally deep placental invasion. Journal of obstetrics and women's diseases. 2022; 71(2): 39-48. (in Russian)]. https://dx.doi.org/10.17816/ JOWD88697.
- Jauniaux E., Jurkovic D., Hussein A.M., Burton G.J. New insights into the etiopathology of placenta accreta spectrum. Am. J. Obstet. Gynecol. 2022; 227: 384-91. https://dx.doi.org/10.1016/j.ajog.2022.02.038.
- Zhou J., Chen H., Xu X., Liu Y., Chen S., Yang S. et al. Uterine damage induces placenta accreta and immune imbalance at the maternal-fetal interface in the mouse. Placenta. 2022; 119: 8-16. https://dx.doi.org/10.1016/ j.placenta.2022.01.002.
- Harris L.K., Benagiano M., D'Elios M.M., Brosens I., Benagiano G. Placental bed research: II. Functional and immunological investigations of the placental bed. Am. J. Obstet. Gynecol. 2019; 221(5): 457-469. https://dx.doi.org/10.1016/ j.ajog.2019.07.010.
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