Placental inflammatory changes associated with mRNA expression of transcription factor genes in term pregnancy


Дәйексөз келтіру

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Аннотация

Objective: To investigate the mRNA expression levels of transcription factor genes (GATA3, RORC2, FOXP3) in the cervical canal, placenta, and fetal membranes in term gestation depending on the presence of histologic chorioamnionitis. Materials and methods: The expression of GATA3, RORC2, and FOXP3 mRNAs was detected in 42pregnant women with a healthy pregnancy who underwent a planned cesarean section for fetal malpresentation and/or uterine scar at 37-41 weeks' gestation. The analysis was performed using RT-PCR and a morphological study of placentas. Results: Histologic chorioamnionitis was detected in 28 (66.7%) patients without clinical manifestations. In the presence of funiculitis/funisitis (7.1%), there was a 10-fold increase in the expression of GATA3 mRNA in the placenta and a 4-fold decrease in the fetal membranes. Parietal chorioamnionitis (64.3%) was associated with a 2-fold increase in expression levels of RORC2 FOXP3 in the placenta. Leukocyte infiltration of the fetal membranes (26.1%) was associated with a 10-fold decrease in the expression of GATA3 mRNA in the cervical canal. Conclusion: The present study showed that more than half of women with a healthy term pregnancy had histological chorioamnionitis. Analysis of the expression of transforming factors GATA3, RORC2, FOXP3 represents a promising direction in diagnosing placental and fetal membranes inflammatory process.

Толық мәтін

Рұқсат жабық

Авторлар туралы

Maria Kaganova

Samara State Medical University, Ministry of Health of Russia

Email: mkaganova@yandex.ru
Ph.D., Associate Professor at the Department of Obstetrics and Gynecology, Institute for Postgraduate Education

Natalia Spiridonova

Samara State Medical University, Ministry of Health of Russia

Email: nvspiridonova@mail.ru
Dr. Med. Sci., Professor, Head of the Department of Obstetrics and Gynecology, Institute for Postgraduate Education

Әдебиет тізімі

  1. Conti N., Torricelli M., Voltolini C., Vannuccini S., Clifton V.L., Bloise E. et al. Term histologic chorioamnionitis: a heterogeneous condition. Eur. J. Obstet. Gynecol. Reprod. Biol. 2015; 188: 34-8. https://dx.doi.org/10.1016/j.ejogrb.2015.02.034.
  2. Lee S.M., Lee K.A., Kim S.M., Park C.W., Yoon B.H. The risk of intra-amniotic infection, inflammation and histologic chorioamnionitis in term pregnant 420 women with intact membranes and labor. Placenta. 2011; 32(7): 516-21. https://dx.doi.org/10.1016/j.placenta.2011.03.012.
  3. Xu Y., Romero R., Miller D., Silva P., Panaitescu B., Theis K.R. et al. Innate lymphoid cells at the human maternal-fetal interface in spontaneous preterm labor. Am. J. Reprod. Immunol. 2018; 79(6): e 12820. https://dx.doi.org/10.1111/aji.12820.
  4. Каткова Н.Ю., Бодрикова О.И., Сергеева А.В., Безрукова И.М., Покусаева К.Б. Состояние локального иммунного статуса при различных вариантах преждевременных родов. Вестник Российского государственного медицинского университета. 2017; 3: 57-61.
  5. Krop J., Heidt S., Claas F.H.J., Eikmans M. Regulatory T. сells in pregnancy: it is not all about FoxP3. Front. Immunol. 2020; 11: 1182. https://dx.doi.org/10.3389/fimmu.2020.01182.
  6. La Rocca C., Carbone F., Longobardi S., Matarese G. The immunology of pregnancy: regulatory T. cells control maternal immune tolerance toward the fetus. Immunol. Lett. 2014.; 162(1, Pt A): 41-8. https://dx.doi.org/10.1016/j.imlet.2014.06.013.
  7. Roberts K.A., Riley S.C., Reynolds R.M., Barr S., Evans M., Statham A. et al. Placental structure and inflammation in pregnancies associated with obesity. Placenta. 2011; 32(3): 247-54. https://dx.doi.org/10.1016/j.placenta.2010.12.023.
  8. Ремнева О.В., Колядо О.В., Песоцкая А.В., Стародубцев Е.Г., Гуменюк И.С. Патоморфологические особенности последов у пациенток с различными клиническими фенотипами спонтанных преждевременных родов. Акушерство и гинекология. 2021; 8: 111-8. [Remneva O.B., Kolyado O.V., Pesotskaya A.V., Starodubtsev E.G., Gumenyuk I.S. Pathomorphological features of placenta in patients with different clinical phenotypes of spontaneous preterm births. Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2021; 8: 111-8. (in Russian)]. https://dx.doi.org/10.18565/aig.2021.8.111-118.
  9. Lee Y.H., Shynlova O., Lye S.J. Stretch-induced human myometrial cytokines enhance immune cell recruitment via endothelial activation. Cell. Mol. Immunol. 2015; 12(2): 231-42. https://dx.doi.org/10.1038/cmi.2014.39.
  10. Kwak-Kim J., Bao S., Lee S.K., Kim J. W., Gilman-Sachs A. Immunological modes of pregnancy loss: inflammation, immune effectors, and stress. Am. J. Reprod. Immunol. 2014; 72(2): 129-40. https://dx.doi.org/10.1111/aji.12234.
  11. Низяева Н.В., Карапетян А.О., Гапаева М.Д., Синицына В.А., Баев О.Р. Структурные особенности плодных оболочек при преждевременных родах. Акушерство и гинекология. 2019; 8: 63-9. [Nizyaeva N.V., Karapetyan AO., Gapaeva M.D., Sinitsyna V.A., Baev O.R. Structural features of fetal membranes in preterm labor. Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2019; 8: 63-9 (in Russian)]. https://dx.doi.org/10.18565/aig.2019.8.63-69.
  12. Хаитов P.M., Ярилин А.А., Пинегин Б.В. Иммунология: атлас. М.: ГЭОТАР-Медиа; 2011. 624с.
  13. Areia A., Vale-Pereira S., Alves V., Rodrigues-Santos P., Moura P., Mota-Pinto A. Membrane progesterone receptors in human regulatory T. cells: a reality in pregnancy. BJOG. 2015; 122(11): 1544-50. https://dx.doi.org/10.1111/1471-0528.13294.
  14. Wilczynski J.R. Immunological analogy between allograft rejection, recurrent abortion and pre-eclampsia - the same basic mechanism? Hum. Immunol. 2006; 67(7): 492-511. https://dx.doi.org/10.1016/j.humimm.2006.04.007.
  15. Bar E., Whitney P.G., Moor K., Reis e Sousa C., LeibundGut-Landmann S. IL-17 regulates systemic fungal immunity by controlling the functional competence of NK cells. Immunity. 2014; 40(1): 117-27. https://dx.doi.org/10.1016/j.immuni.2013.12.002.
  16. Tsuda S., Zhang X., Hamana H., Shima T., Ushijima A., Tsuda K. et al. Clonally expanded decidual effector regulatory T. cells increase in late gestation of normal pregnancy, but not in preeclampsia, in humans. Front. Immunol. 2018; 9: 1934. https://dx.doi.org/10.3389/fimmu.2018.01934.
  17. Bourmenskaya O., Bayramova G., Nepsha O., Rebrikov D., Trofimov D., Muravieva V., Sukhikh G. Vaginal smear TNF-alpha, IL18, TLR4, and GATA3 mRNA levels correlate with local inflammation. Int. J. Biomed. 2014; 4(4): 204-8.
  18. Chen J., Shi Y., Huang J., Luo J., Zhang W. Neuromedin B. receptor mediates neuromedin B-induced COX-2 and IL-6 expression in human primary myometrial cells. J. Investig. Med. 2020; 68(6): 1171-8. https://dx.doi.org/10.1136/jim-2020-001412.
  19. Zhang C., Wang W. Liu C., Lu J., Sun K. Role of NF-kB/GATA3 in the inhibition of lysyl oxidase by IL-1b in human amnion fibroblasts. Immunol. Cell Biol. 2017; 95(10): 943-52. https://dx.doi.org/10.1038/icb.2017.73.
  20. Крукиер И.И., Левкович М.А., Авруцкая В.В., Чурюкина Э.В., Никашина А.А., Чикина Л.Г. Роль продукции цитокинов, органических кислот в сыворотке крови и амниотической жидкости в развитии спонтанных преждевременных родов. Акушерство и гинекология. 2021; 9: 60-5. [Krukier I.I., Levkovich M.A., Avrutskaya V.V., Churyukina E.V., Nikashina A.A., Chikina L.G. The role of cytokines and organic acids production in the blood serum and amniotic fluid in spontaneous preterm labor. Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2021; 9: 60-5. (in Russian)]. https://dx.doi.org/10.18565/aig.2021.9.60-65.
  21. Щеголев А.И. Современная морфологическая классификация повреждений плаценты. Акушерство и гинекология. 2016; 4: 16-23. [Shchegolev A.I. Current morphological classification of damages to the placenta. Akusherstvo i Ginekologiya/Obstetrics and Gynecology. 2016; 4: 16-23. (in Russian)]. https://dx.doi.org/10.18565/aig.2016.4.16-23.
  22. Щеголев А.И., Дубова Е.А., Павлов К.А. Морфология плаценты. Пособие для врачей. М.: Форза; 2010. 46с.
  23. Lima J., Martins C., Nunes G., Sousa M.J., Branco J.C., Borrego L.M. Regulatory T. сells show dynamic behavior during late pregnancy, delivery, and the postpartum period. Reprod. Sci. 2017; 24(7): 1025-32. https://dx.doi.org/10.1177/1933719116676395.
  24. Romero R., Pacora P., Kusanovic J., Jung E., Panaitescu B., Maymon E. et al. Clinical chorioamnionitis at term X: microbiology, clinical signs, placental pathology, and neonatal bacteremia - implications for clinical care. J. Perinat. Med. 2021; 49(3): 275-98. https://dx.doi.org/10.1515/jpm-2020-0297.
  25. Курносенко И.В., Долгушина В.Ф., Пастернак А.Е. Воспалительные изменения в последе у женщин в преждевременными и своевременными родами. Современные проблемы науки и образования. 2016; 3: 172.
  26. Будиловская О.В., Шипицына Е.В., Переверзева Н.А., Воробьева Н.Е., Спасибова Е.В., Григорьев А.Н., Савичева А.М. Сравнение методов оценки воспалительной реакции нижних отделов женского репродуктивного тракта. Журнал акушерства и женских болезней. 2018; 67(5): 13-20. [Budilovskaya O.V., Shipitsina E.V., Pereverzneva N.A., Vorobyova N.E., Spasibova E.V., Grigoryev AN. et al. Comparison of methods for assessing the inflammatory response of the lower parts of the female reproductive tract. Zhurnal akusherstva i zhenskikh boleznei/Journal of Obstetrics and Women's Diseases. 2018; 67(5): 13-20. (in Russian)]. https://dx.doi.org/10.17816/ JOWD67513-20.
  27. Гомболевская Н.А., Бурменская О.В., Демура Т.А., Марченко Л.А., Коган Е.А., Трофимов Д.Ю., Сухих Г.Т. Оценка экспрессии мРНК генов цитокинов в эндометрии при хроническом эндометрите. Акушерство и гинекология. 2013; 11: 35-40.
  28. Низяева Н.В. Гистологические критерии воспалительных изменений плодных оболочек плаценты и пуповины. Международный журнал прикладных и фундаментальных исследований. 2018; 3: 180-8.
  29. Меджидова М.К., Бурменская О.В., Донников А.Е., Непша О.С., Трофимов Д.Ю., Касабулатов Н.М., Тютюнник В.Л., Сухих Г.Т. Оценка локальной воспалительной реакции во влагалище по профилю экспрессии мРНК генов цитокинов у беременных накануне родов. Акушерство и гинекология. 2012; 3: 26-31.
  30. Ganjalikhani Hakemi M., Ghaedi K., Homayouni V., Andalib A., Hosseini M., Rezaei A. Positive and negative regulation of Th17 cell differentiation: evaluating the impact of RORC2. Cell J. 2014 Autumn; 16(3): 343-52.
  31. Eghbal-Fard S., Yousefi M., Heydarlou H., Ahmadi M., Taghavi S., Movasaghpour A. et al. The imbalance of Th17/Treg axis involved in the pathogenesis of preeclampsia. J. Cell. Physiol. 2019; 234(4): 5106-16. https://dx.doi.org/10.1002/jcp.27315.
  32. Figueiredo A.S., Schumacher A. The T. helper type 17/regulatory T. cell paradigm in pregnancy. Immunology. 2016; 148(1): 13-21. https://dx.doi.org/10.1111/imm.12595.

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