Modulation of the interaction between NK-cells and trophoblast by intravenous immunoglobulin
- Authors: Mikhailova V.A.1, Davydova A.A.1, Bazhenov D.O.1, Kovaleva A.A.1, Zagaynova V.A.1, Kogan I.Y.1, Bespalova O.N.1, Gzgzyan A.M.1, Sokolov D.I.1, Selkov S.A.1
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Affiliations:
- D.O. Ott Research Institute for Obstetrics, Gynecology and Reproductology
- Issue: No 6 (2022)
- Pages: 105-113
- Section: Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/249567
- DOI: https://doi.org/10.18565/aig.2022.6.105-113
- ID: 249567
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Abstract
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About the authors
Valentina A. Mikhailova
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologySenior Researcher at the Laboratory of Intercellular Interactions, Department of Immunology and Intercellular Interactions
Alina A. Davydova
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyJunior Researcher at the Laboratory of Intercellular Interactions, Department of Immunology and Intercellular Interactions
Dmitriy O. Bazhenov
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyJunior Researcher at the Laboratory of Intercellular Interactions, Department of Immunology and Intercellular Interactions
Anastasia A. Kovaleva
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyLaboratory Technician at the Laboratory of Intercellular Interactions, Department of Immunology and Intercellular Interactions
Valeriya A. Zagaynova
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyJunior Researcher, obstetrician-gynecologist at the Department of Assisted Reproductive Technologies
Igor Yu. Kogan
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyCorresponding Member of RAS, Dr. Med. Sci., Professor, Director
Olesya N. Bespalova
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyDr. Med. Sci., Deputy Director
Alexandr M. Gzgzyan
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyDr. Med. Sci, Head of the Department of Assisted Reproductive Technologies
Dmitry I. Sokolov
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyDr. Bio. Sci., Head of the Laboratory of Intercellular Interactions, Department of Immunology and Intercellular Interactions
Sergey A. Selkov
D.O. Ott Research Institute for Obstetrics, Gynecology and ReproductologyMerited Scolar of the Russian Federation, Professor, Head of the Department of Immunology and Intercellular Interactions
References
- Robertson S.A., Jin M., Yu D., Moldenhauer L.M., Davies M.J., Hull M.L., Norman R.J. Corticosteroid therapy in assisted reproduction - immune suppression is a faulty premise. Hum. Reprod. 2016; 31(10): 2164-73. https://dx.doi.org/10.1093/humrep/dew186.
- Makrigiannakis A., Petsas G., Toth B., Relakis K., Jeschke U. Recent advances in understanding immunology of reproductive failure. J. Reprod. Immunol. 2011; 90(1): 96-104. https://dx.doi.org/1016/jad2011.03.006.
- Агнаева А.О., Беспалова О.Н., Соколов Д.И., Сельков С.А., Коган И.Ю. Роль естественных киллеров (NK-клеток) в репродуктивных потерях. Журнал акушерства и женских болезней. 2017; 66(3): 143-156. https://dx.doi.org/10.17816/jowd663143-156.
- Lee S.K., Na B.J., Kim J.Y., Hur S.E., Lee M., Gilman-Sachs A. et. al. Determination of clinical cellular immune markers in women with recurrent pregnancy loss. Am. J. Reprod. Immunol. 2013; 70(5): 398-411. https://dx.doi.org/10.1111/aji.12137.
- Ahmadi M., Ghaebi M., Abdolmohammadi-Vahid S., Abbaspour-Aghdam S., Hamdi K., Abdollahi-Fard S. et al. NK cell frequency and cytotoxicity in correlation to pregnancy outcome and response to IVIG therapy among women with recurrent pregnancy loss. J. Cell Physiol. 2019; 234(6): 9428-37. https://dx.doi.org/10.1002/jcp.27627.
- Sacks G., Yang Y., Gowen E., Smith S., Fay L., Chapman M. Detailed analysis of peripheral blood natural killer cells in women with repeated IVF failure. Am. J. Reprod. Immunol. 2012; 67(5): 434-42. https://dx.doi.org/10.1111/j.1600-0897.2012.01105.x.
- Salazar M.D., Wang W.J., Skariah A., He Q., Field K., Nixon M. et al. Post-hoc evaluation of peripheral blood natural killer cell cytotoxicity in predicting the risk of recurrent pregnancy losses and repeated implantation failures. J. Reprod. Immunol. 2022; 150: 103487. https://dx.doi.org/10.1016/j.jri.2022.103487.
- Seshadri S., Sunkara S.K. Natural killer cells in female infertility and recurrent miscarriage: a systematic review and meta-analysis. Hum. Reprod. Update. 2014; 20(3): 429-38. https://dx.doi.org/10.1093/humupd/dmt056.
- Karami N., Boroujerdnia M.G., Nikbakht R., Khodadadi A. Enhancement of peripheral blood CD56(dim) cell and NK cell cytotoxicity in women with recurrent spontaneous abortion or in vitro fertilization failure. J. Reprod. Immunol. 2012; 95(1-2): 87-92. https://dx.doi.org/10.1016/j.jri.2012.06.005.
- Polanski L.T., Barbosa M.A., Martins W.P., Baumgarten M.N., Campbell B., Brosens J. et al. Interventions to improve reproductive outcomes in women with elevated natural killer cells undergoing assisted reproduction techniques: a systematic review of literature. Hum. Reprod. 2014; 29(1): 65-75. https://dx.doi.org/10.1093/humrep/det414.
- Ho Y.K., Chen H.H., Huang C.C., Lee C.I., Lin P.Y., Lee M.S. et al. Peripheral CD56( + )CD16(+) NK cell populations in the early follicular phase are associated with successful clinical outcomes of intravenous immunoglobulin treatment in women with repeated implantation railure. Front. Endocrinol. (Lausanne). 2019; 10: 937. https://dx.doi.org/10.3389/fendo.2019.00937.
- Chernyshov V.P., Dons'koiB.V., Sudoma I.O., Goncharova Y.O. Multiple immune deviations predictive for IVF failure as possible markers for IVIG therapy. Immunol. Lett. 2016; 176: 44-50. https://dx.doi.org/10.1016/j.imlet.2015.12.010
- Shimada S., Takeda M., Nishihira J., Kaneuchi M., Sakuragi N., Minakami H. et al. A high dose of intravenous immunoglobulin increases CD94 expression on natural killer cells in women with recurrent spontaneous abortion. Am. J. Reprod. Immunol. 2009; 62(5): 301-7. https://dx.doi.org/10.1111/j.1600-0897.2009.00739.x.
- Han A.R., Lee S.K. Immune modulation of i.v. immunoglobulin in women with reproductive failure. Reprod. Med. Biol. 2018; 17(2): 115-24. https://dx.doi.org/10.1002/rmb2.12078.
- Apps R., Murphy S.P., Fernando R., Gardner L., Ahad T., Moffett A. Human leucocyte antigen (HLA) expression of primary trophoblast cells and placental cell lines, determined using single antigen beads to characterize allotype specificities of anti-HLA antibodies. Immunology. 2009; 127(1): 26-39. https://dx.doi.org/10.1111/j.1365-2567.2008.03019.x.
- Huhn O., Zhao X., Esposito L., Moffett A., Colucci F., Sharkey A.M. How do uterine natural Killer and innate lymphoid cells contribute to successful pregnancy? Front. Immunol. 2021; 12: 607669. https://dx.doi.org/10.3389/fimmu.2021.607669.
- Gong J.H., Maki G., Klingemann H.G. Characterization of a human cell line (NK-92) with phenotypical and functional characteristics of activated natural killer cells. Leukemia. 1994; 8(4): 652-8.
- Drew S.I., Terasaki P.I., Billing R.J., Bergh O.J., Minowada J., Klein E. Group-specific human granulocyte antigens on a chronic myelogenous leukemia cell line with a Philadelphia chromosome marker. Blood. 1977; 49(5): 715-8.
- Kohler P.O., Bridson W.E. Isolation of hormone-producing clonal lines of human choriocarcinoma. J. Clin. Endocrinol. Metab. 1971; 32(5): 683-7. https://dx.doi.org/10.1210/jcem-32-5-683.
- Manaster I., Goldman-Wohl D., Greenfield C., Nachmani D., Tsukerman P., Hamani Y. et al. MiRNA-mediated control of HLA-G expression and function. PLoS One. 2012; 7(3): e33395. https://dx.doi.org/10.1371/journal.pone.0033395.
- Bespalova 0., Bakleicheva M., Ivashchenko T., Tral T., Tolibova G., Kogan I. Expression of HLA-G and KIR2DL4 receptor in chorionic villous in missed abortion. Gynecol. Endocrinol. 2020; 36(Suppl. 1): 43-7. https://dx.doi.org/10.1080/09513590.2020.1816716.
- Robson A., Lash G.E., Innes B.A., Zhang J.Y., Robson S.C., Bulmer J.N. Uterine spiral artery muscle dedifferentiation. Hum. Reprod. 2019; 34(8): 1428-38. https://dx.doi.org/10.1093/humrep/dez124.
- Arumugam T.V., Tang S.C., Lathia J.D., Cheng A., Mughal M.R., Chigurupati S. et al. Intravenous immunoglobulin (IVIG) protects the brain against experimental stroke by preventing complement-mediated neuronal cell death. Proc. Natl. Acad. Sci. USA. 2007; 104(35): 14104-9. https://dx.doi.org/10.1073/pnas.0700506104.
- Zhu C., Anderson A.C., Schubart A., Xiong H., Imitola J., Khoury S.J. et al. The Tim-3 ligand galectin-9 negatively regulates T. helper type 1 immunity. Nat. Immunol. 2005; 6(12): 1245-52. https://dx.doi.org/10.1038/ni1271.
- Wang F., Hou H., Wu S., Tang Q., Huang M., Yin B. et al. Tim-3 pathway affects NK cell impairment in patients with active tuberculosis. Cytokine. 2015; 76(2): 270-9. https://dx.doi.org/10.1016/j.cyto.2015.05.012.
- So E.C., Khaladj-Ghom A., Ji Y., Amin J., Song Y., Burch E. et al. NK cell expression of Tim-3: First impressions matter. Immunobiology. 2019; 224(3): 362-70. https://dx.doi.org/10.1016/j.imbio.2019.03.001.
- Holmannova D., Kolackova M., Kondelkova K., Kunes P., Krejsek J., Andrys C. CD200/CD200R paired potent inhibitory molecules regulating immune and inflammatory responses; Part I: CD200/CD200R structure, activation, and function. Acta Medica (Hradec Kralove). 2012; 55(1): 12-7. https://dx.doi.org/10.14712/18059694.2015.68.
- Barclay A.N., Wright G.J., Brooke G., Brown M.H. CD200 and membrane protein interactions in the control of myeloid cells. Trends Immunol. 2002; 23(6): 28590. https://dx.doi.org/10.1016/s1471-4906(02)02223-8.
- Clark D.A., Wong K., Banwatt D., Chen Z., Liu J., Lee L. et al. CD200-dependent and nonCD200-dependent pathways of NK cell suppression by human IVIG. J. Assist. Reprod. Genet. 2008; 25(2-3): 67-72. https://dx.doi.org/10.1007/s10815-008-9202-9.
- Сельков С.А., Соколов Д.И., Чепанов С.В. Иммунорегуляторные эффекты иммуноглобулинов для внутривенного введения. Медицинская иммунология. 2013; 15(1): 5-12.