对早期妊娠流产胎儿进行全面分子形态学研究的结果

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论证。胎儿停育导致早期妊娠孕囊排出的主要原因。在本病的病因中,遗传原因是最主要原因。目前,免疫方面的母体-胎儿系统广泛讨论。在这方面,根据绒毛膜的核型,以及孕囊排出后,研究胎儿停育期间母体和胎儿之间的免疫关系的特征是一项紧迫的问题。这可以优化胎儿停育患者的筛查,并确定导致习惯性流产的因素。

本研究的目的是根据绒毛膜染色体异常的存在和患者孕囊排出史,研究胎儿停育中流产胎儿的形态学和免疫组化特征。

材料与方法。对273例胎儿停育的流产胎儿进行了全面的形态学和免疫组织化学研究(CD56、 HLA-DR-II)。第一组包括有不同变异的绒毛膜染色体异常的病人(n=169),第二组包括正常绒毛膜核型的病人(n=104)。根据孕囊排出的存在,考虑到患者的病史,并对数据进行了分析。

结果。该研究揭示了绒毛膜染色体异常的胎儿停育中流产胎儿的形态特征:绒毛明显水肿、增厚、坏死,更严重的炎症变化为蜕膜组织和子宫内膜的中度至重度淋巴细胞和巨噬细胞浸润,其中白细胞按微脓肿类型积聚。已证明,流产胎儿中炎症变化的严重程度仅受绒毛膜核型的影响,不受无活胚卵在宫腔内存留时间的影响,也不受患者病历中出现孕囊排出的影响。研究表明,流产胎儿中的CD56和HLA-DR II类水平取决于患者孕囊排出的病史,而与绒毛膜核型无关。

结论。因此,对于没有妇科疾病的患者,在初次胎儿停育时,只需要采用绒毛膜核型来确定胎儿停育的原因;而对重复胎儿停育进行CD56和HLA-DR II类标志物的免疫组化检测是有意义的。

作者简介

Olga A. Romanova

North-Western State Medical University named after I.I. Mechnikov

Email: romanova-roa@yandex.ru
ORCID iD: 0000-0003-2637-5620
SPIN 代码: 5740-7953
Researcher ID: ААВ-2136-2021

MD, obstetrician-gynecologist of the Department of Gynecology

俄罗斯联邦, 41, Kirochnaya St., Saint Petersburg, 191015

Victoria A. Pechenikova

North-Western State Medical University named after I.I. Mechnikov

编辑信件的主要联系方式.
Email: p-vikka@mail.ru
SPIN 代码: 9603-5645
Researcher ID: ААВ-2105-2021

MD, Dr. Sci. (Med.), PhD, Professor of the Department of Obstetrics and Gynecology

俄罗斯联邦, 41, Kirochnaya St., Saint Petersburg, 191015

参考

  1. Tral TG, Tolibova GK, Serdiukov SV, Polyakova VO. Morphofunctional evaluation of the causes of stilled pregnancy in the first trimester. Journal of obstetrics and women’s diseases. 2013;62(3):83–87. (In Russ.). doi: 10.17816/JOWD62383-87
  2. Sidelnikova VM. Privychnaya poterya beremennosti. Moscow: Triada-X; 2005. (In Russ.)
  3. Bulletti C, Flamigni C, Giacomuccii E. Reproductive failure due to spontaneous abortion and recurrent miscarriage. Hum Reprod Update. 1996;2(2):118–136. doi: 10.1093/humupd/2.2.118
  4. Sotnikova NYu, Voronun DN, Anciferova YuS. The role of decidual CD56+ natural killers in regulation of the local immune response during early pregnancy. Journal of Ural Medical Academic Science. 2011;2–1(35):68–69. (In Russ.)
  5. Kozyreva EV, Davidyan LY. Immunohistochemical features of chronic endometritis in case of infertility and miscarriage (review of literature). University proceedings. Volga region. Medical sciences. 2015:4(36):124–136. (In Russ.)
  6. Agnaeva AO, Bespalova ON, Sokolov DI, et al. Role of natural killer cells in reproductive failure. Journal of obstetrics and womans diseases. 2017;66(3):143–156. (In Russ.). doi: 10.17816/jowd663143-156
  7. Mikhailova VA, Selkov SA, Sokolov DI. Phenotypic and functional characteristics of NK cells in pregnancy. Obstetrics and Gynecology. 2011;(5):4–9. (In Russ.)
  8. Sharma S. Natural killer cells and regulatory T cells in early pregnancy loss. Int J Dev Biol. 2014;58(2–4):219–229. doi: 10.1387/ijdb.140109ss
  9. Zhang X, Li J, Gu Yi, et al. A pilot study on environmental and behavioral factors related to missed abortion. Environ Health Prev Med. 2011;16(4):273–278. doi: 10.1007/s12199-010-0196-4
  10. Mustafina LR, Khon EV, Logvinov SV, Yuriyev SYu. Cellular composition of decidua basalis infiltrate during early pregnancy in urogenital mycoplasma infection. Morphology. 2011;139(3):72–76. (In Russ.)
  11. Reinke P, Volk HD. Diagnostic and predictive value of an immune monitoring program for complications after kidney transplantation. Urol Int. 1992;49(2):69–75. doi: 10.1159/000282398.
  12. Reinke P, Fietze E, Docke WD, et al. Late acute rejection in long-term renal allograft recipients. Diagnostic and predictive value of circulating activated T cells. Transplantation. 1994;58(1):35–41.
  13. Henny FC, Weening JJ, Baldwin WM, et al. Expression of HLA-DR antigens on peripheral blood T lymphocytes and renal graft tubular epithelial cells in association with rejection. Transplantation. 1986;42(5):479–483. doi: 10.1097/00007890-198611000-00007
  14. Loewendorf AI, Nguyen TA, Yesayan MN, et al. Normal human pregnancy results in Maternal Immune Activation in the Periphery and at the Uteroplacental Interface. PLoS One. 2014;9(5):e96723. doi: 10.1371/journal.pone.0096723
  15. Ellinidi VN, Davydova NI, Kalinina NM, et al. Modern opportunities for diagnostics of chronic endometritis. Journal of obstetrics and womans diseases. 2003;52(3):64–68. (In Russ.)
  16. Demidova EM. Privychnyj vykidysh (patogenez, akusherskaja taktika) [dissertation] Moscow; 1993. (In Russ.). [cited 16 Aug 2021.] Available from: http://medical-diss.com/docreader/405801/a?#?page=1
  17. Akulich NS, Runets UF, Yudina OA, Sheviako AD. Morphological criteria for miscarriage of early pregnancy. Medical Journal. 2017;3(61):49–52. (In Russ.)
  18. Khelnitsky OK. Tsitologicheskaya i gistologicheskaya diagnostika zabolevaniy sheyki i tela matki. St. Petersburg: SOTIS; 1999. (In Russ.)
  19. Peretyatko LP, Fateeva NV, Kuznetsov RA, Malyshkina AI. The comparative morphology of the villous chorion at 5−12 week pregnancy at the chronic endometritis complicated by habitual miscarriage and artificial abortions. Tavricheskiy Mediko-Biologicheskiy Vestnik. 2017;20(2–2):98–103. (In Russ.)
  20. Zakharov GA, Galiulina EV, Zarechnova NN. Structure of ovum of abortive material of human embryos with non-viable pregnancy with sexually transmitted diseases. Tambov University Reports. Series Natural and Technical Sciences. 2014:19(6):2001–2003. (In Russ.)

补充文件

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1. JATS XML
2. 图1 染色体异常的绒毛:合并明显的增厚和水肿, 滋养细胞坏死,绒毛间的纤维素坏死区。苏木精-伊红染色,增大×100倍

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3. 图2 染色体绒毛膜异常的蜕膜组织(微脓肿)苏木精-伊红染色,增大×100倍

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4. 图3 染色体绒毛膜异常中子宫内膜的微脓肿苏木精-伊红染色,增大×100倍

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5. 图4 根据孕囊排出史,胎儿停育患者子宫内膜和蜕膜组织中CD56和HLA-DR类II的免疫组织化学研究

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6. 图5 CD56免疫组织化学显微镜照片:a——在初次胎儿停育的病人的子宫内膜中;b——在初次胎儿停育的病人的蜕膜组织中;c——在一个有孕囊排出史病人的子宫内膜中;d——在一个有孕囊排出史病人的蜕膜组织中。免疫组织化学检查,增大×400陪

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7. 图6 HLA-DR II级免疫组织化学显微镜照片:a——在初次胎儿停育的病人的子宫内膜中;b——在初次胎儿停育的病人的蜕膜组织中;c——在一个有孕囊排出史病人的子宫内膜中;d——在一个有孕囊排出史病人的蜕膜组织中。免疫组织化学检查,增大×400陪

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