References
1. Renaud S.J., Graham C.H. The role of macrophages in utero/placental interaction during normal and pathological pregnancy. Immunol. Invest. 2008; 37 (5): 535–64. DOI: https://doi.org/10.1080/088201130802191375
2. Minoz-Suano A., Hamilton A.B., Betz A.G. Gimme shelter: the immune system during pregnancy. Immunol. Rev. 2011; 241 (1): 2038. DOI: https://doi.org/10.1111/j.1600-065X.2011.01002.x
3. Ning F., Liu H., Lash G.E. The role of decidual macrophages during normal and pathological pregnancy. Am. J. Reprod. Immunol. 2016; 75 (3): 298–309. DOI: https://doi.org/10.1111/aji.12477
4. Maloy K. J., Salaun L., Cahill R., Dougan G., Saunders N. J., Powrie F. CD4+CD25+TR cells suppress innate immune pathology through cytokine-dependent mechanism. J. Exp. Med. 2003; 197: 111–9. DOI: https://doi.org/10.1084/jem.20021345
5. Connor R.A., Anderton S.M. Inflammation-associated genes: risks and benefits to Foxp3+ regulatory T-cell function. Immunology. 2015; 146: 194–205. DOI: https://doi.org/10.1111/imm.12507
6. Ng T.H., Britton G.J., Hill E.V., Verhagen J., Burton B.R., Wraith D.C. Regulation of adaptive immunity: role of interleukin-10. Front. Immunol. 2013; 4: 129. DOI: https://doi.org/10.3389/fimmu.2013.00129
7. Saraiva M., Vieira P., O’Garra A. Biology and therapeutic potential of interleukin-10. J. Exp. Med. 2020; 217 (1): e20190418. DOI: https://doi.org/10.1084/jem.20190418
8. Guzman-Genuino R.M., Diener K.R. Regulatory B cells in pregnancy: lessons from autoimmunity, graft tolerance, and cancer. Front. Immunol. 2017; 8: 172. DOI: https://doi.org/10.3389/fimmu.2017.00172
9. Li M.O., Flavell R.A. TGF-beta: a master of all T cell trades. Cell. 2008; 134: 392–404. DOI: https://doi.org/10.1016/j.cell.2008.07.025
10. Yoshimura A., Wakabayashi Y., Mori T. Cellular and molecular basis for the regulation of inflammation by TGF-beta. J. Biochem. 2010; 147 (6): 781–92. DOI: https://doi.org/10.1093/jb/mvq043
11. Liu Y.Z., Zhang P., Li J., Kulkarni A.B., Perruche S., Chen W.J. A critical function for TGF-beta signaling in the development of natural CD4+CD25+Foxp3+ regulatory T cells. Nat. Immunol. 2008. Vol. 9. P. 632–40. DOI: https://doi.org/10.1038/ni.1607
12. Pyzik M., Piccirillo C.A. TGF-β modulates Foxp3 expression and regulatory activity in distinct CD4 T cell subsets. J. Leukoc. Biol. 2007; 82: 335–46. DOI: https://doi.org/10.1189/jlb.1006644
13. Qiu T., Teng Y., Wang Y., Xu L. Adoptive transfer of transforming growth factor-β1-induced CD4+CD25+ regulatory T cells prevents immune response-mediated spontaneous abortion. Reprod. Fertil. Dev. 2015 May 14. DOI: https://doi.org/10.1071/RD14503
14. Lao K., Zhao M., Li Zh., Liu X., Zhang H., Jiang Y., Wang Y., Hu X. IL-10 regulate decidual Tregs apoptosis contributing to the abnormal pregnancy with Toxoplasma gondii infection. Microb. Pathog. 2015; 89: 210–6. DOI: https://doi.org/10.1016/j.micpath.2015.10.002
15. Zhao M., Zhang R., Xu X., Liu Y., Zhang H., Zhai X., Hu X. IL-10 reduces levels of apoptosis in Toxoplasma gondii-infected trophoblasts. PLoS One. 2013; 8 (2): e56455. DOI: https://doi.org/10.1371/journal.pone.0056455
16. Zhao M., Zhang H., Liu X., Jiang Y., Ren L., Hu X. The effect of TGF-β on Treg cells in adverse pregnancy outcome upon Toxoplasma gondii infection Front. Microbiol. 2017; 8: 901. DOI: https://doi.org/10.3389/fmicb.2017.00901
17. Clark D.A. On use of animal models. Emerg. Top. Life Sci. 2020; 4 (2): 207–27. DOI: https://doi.org/10.1042/ETLS20200042
18. Gendron R.L., Baines M.G. Morphometric analysis of the histology of spontaneous fetal resorption in a murine pregnancy. Placenta. 1989; 10 (3): 309–18. DOI: https://doi.org/10.1016/0143-4004(89)90031-3
19. Kwak-Kim J., Park J.C., Ahn H.K., Kim J.W., Gilman-Sachs A. Immunological modes of pregnancy loss. Am. J. Reprod. Immunol. 2010; 63 (6): 611–23. DOI: https://doi.org/10.1111/j.1600-0897.2010.00847.x
20. Thuere C., Zenclussen M.L., Schumacher A., Langwisch S., Schulte-Wrede U., Teles A., Paeschke S., Volk H.D., Zenclussen A.C. Kinetics of regulatory T cells during murine pregnancy. Am. J. Reprod. Immunol. 2007; 58 (6): 514–23. DOI: https://doi.org/10.1111/j.1600-0897.2007.00538.x
21. Artem’eva K.A., Bogdanova I.M., Stepanova I.I., Boltovskaya M.N., Kalyuzhin O.V., Stepanov A.A., Zemlyakov A.E. Features of the immune microenvironment in the placenta and gravidar endometrium in mice with spontaneous, induced and potentiated abortions. Immunologiya. 2019; 40 (6): 26–33. DOI: https://doi.org/10.24411/0206-4952-2019-16004 (in Russian)
22. Aeffner F., Wilson K., Martin N.T., Black J.C., Luengo Hendriks C.L., Bolon B., Rudmann D.G., Gianani R., Koegler S.R., Krueger J., Young G.D. The gold standard paradox in digital image analysis: manual versus automated scoring as ground truth. Arch. Pathol. Lab. Med. 2017; 141 (9): 1267–75. DOI: https://doi.org/10.5858/arpa.2016-0386-RA
23. Sykes L., MacIntyre D., Yap Xiao J., Teoh T.G., Bennett Ph.P. The Th1:Th2 dichotomy of pregnancy and preterm labour. Mediators Inflamm. 2012; 2012: 967629. DOI: https://doi.org/10.1155/2012/967629
24. Zingariello M., Ruggeri A., Martelli F., Marra M., Sancillo L., Ceglia I., Rana R.A., Migliaccio A.R. A novel interaction between megakaryocytes and activated fibrocytes increases TGF-β bioavailability in the Gata1(low) mouse model of myelofibrosis. Am. J. Blood Res. 2015; 5 (2): 34–61.
25. Kubiczkova L., Sedlarikova L., Hajek R., Sevcikova S. TGF-β – an excellent servant but a bad master. J. Transl. Med. 2012; 10: 183. DOI: https://doi.org/10.1186/1479-5876-10-183
26. Artem’evа K.A., Kalyuzhin O.V., Stepanova I.I., Nazimovа S.V., Boltovskaya M.N. Morphofunctional characteristics of the immune system and placenta in allogeneic pregnancy in mice high fertility and muramyldipeptides-induced abortion. Klinicheskaya i eksperimental’naya morfologiya. 2013; (4): 34–40. (in Russian)