Cytokine profile of seminal plasma and effectiveness of assisted reproductive technology programs
- Authors: Arefieva A.S.1, Babayan A.A.1, Kalinina E.A.1, Nikolaeva M.A.1
-
Affiliations:
- V. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
- Issue: Vol 24, No 3 (2021)
- Pages: 391-398
- Section: SHORT COMMUNICATIONS
- Submitted: 22.06.2021
- Accepted: 20.08.2021
- Published: 15.07.2021
- URL: https://rusimmun.ru/jour/article/view/1031
- DOI: https://doi.org/10.46235/1028-7221-1031-CPO
- ID: 1031
Cite item
Full Text
Abstract
Increasing evidence shows that seminal plasma is among the most important immunoregulatory factors in female reproductive function. We suggest that the favorable effect of the partner’s seminal plasma (SP) upon pregnancy occurence in women during the cycle of in vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) may be provided by the balanced content of Th1/Th2-dependent seminal cytokines. Otherwise, in case of pathologic changes in SP composition, it may negatively affect the IVF efficiency. Our aim was to determine whether the levels of seminal IL-1β, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-18, IFNγ, TNFα, TNFβ and TGF-β1 are associated with pregnancy establishment in female patients exposed to seminal plasma during IVF/ICSI cycle.
Twenty-eight female patients were exposed to seminal plasma via sexual intercourse before the day of oocyte retrieval, and also underwent intravaginal application of seminal plasma just after transvaginal puncture and oocyte retrieval. Quantitative measurement of seminal cytokines was performed by FlowCytomix™ technology. IL-1, IL-18 and TNFβ concentrations were significantly higher in non-pregnant group (p = 0.011; p = 0.030 and p = 0.008, respectively). The contents of IL-2, IL-6, IL-18 and TNFβ per ejaculate were also significantly higher in non-pregnant group (p = 0.020; р = 0.042; р = 0.030 and р = 0.004, respectively). We conclude that elevated concentrations of proinflammatory cytokines in seminal plasma, as well as their total excessive content per ejaculate may have an adverse effect on implantation and pregnancy establishment.
Keywords
About the authors
A. S. Arefieva
V. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Author for correspondence.
Email: a_arefeva@oparina4.ru
Arefieva Alla S. - LResearch Associate, Laboratory of Clinical Immunology
117997, Moscow, Acad. Oparin str., 4
Russian FederationA. A. Babayan
V. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: a_babayan@oparina4.ru
PhD (Medicine), Obstetrician-gynecologist, Department of Assisted Technologies in Treatment of Infertility
117997, Moscow, Acad. Oparin str., 4
Russian FederationE. A. Kalinina
V. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: e_kalinina@oparina4.ru
PhD, MD (Medicine), Obstetriciangynecologist, Head, Department of Assisted Technologies in Treatment of Infertility
117997, Moscow, Acad. Oparin str., 4
Russian FederationM. A. Nikolaeva
V. Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology
Email: nikolaeva_ma@mail.ru
Leading Research Associate, Laboratory of Clinical Immunology
117997, Moscow, Acad. Oparin str., 4
Russian FederationReferences
- Chen J.C., Johnson B.A., Erikson D.W., Piltonen T.T., Barragan F., Chu S., Kohgadai N., Irwin J.C., Greene W.C., Giudice L.C., Roan N.R. Seminal plasma induces global transcriptomic changes associated with cell migration, proliferation and viability in endometrial epithelial cells and stromal fibroblasts. Hum. Reprod., 2014, Vol. 29, no. 6, pp. 1255-1270.
- Dinarello C.A., Novick D., Kim S., Kaplanski G. Interleukin-18 and IL-18 binding protein. Front. Immunol., 2013, Vol. 4, 289. doi: 10.3389/fimmu.2013.00289.
- Edwards R.G. Human implantation: the last barrier in assisted reproduction technologies? Reprod. Biomed. Online, 2006, Vol. 13, no. 6, pp. 887-904.
- King A., Wheeler R., Carter N.P., Francis D.P., Loke Y.W. The response of human decidual leukocytes to IL-2. Cell. Immunol., 1992, Vol. 141, pp. 409-421.
- Laham N., Dunné F.V., Abraham L.J., Farrugia W., Bendtzen K., Brennecke S.P., Rice G.E. Tumor necrosis factor-beta in human pregnancy and labor. J. Reprod. Immunol., 1997, Vol. 33, no. 1, pp. 53-69.
- Laskarin G., Strbo N., Crncic T.B., Juretic K., Bataille N.L., Chaouat G., Rukavina D. Physiological role of IL-15 and IL-18 at the maternal-fetal interface. Chem. Immunol. Allergy, 2005, Vol. 89, pp. 10-25.
- Makkar G., Ng E.H.Y., Yeung W.S.B., Ho P.C. Excessive ovarian response is associated with increased expression of interleukin-2 in the periimplantation endometrium. Fertil. Steril., 2009, Vol. 91, no. 4, pp. 1145-1151.
- Massagué J. How cells read TGF-beta signals. Nat. Rev. Mol. Cell Biol., 2000, Vol. 1, pp. 169-178.
- Pellicer A., Albert C., Garrido N., Navarro J., Remohi J., Simon C. The pathophysiology of endometriosisassociated infertility: follicular environment and embryo quality. J. Reprod. Fertil. Suppl., 2000, Vol. 55, pp. 109-119.
- Politch J.A., Tucker L., Bowman F.P., Anderson D.J. Concentrations and significance of cytokines and other immunologic factors in semen of healthy fertile men. Hum. Reprod., 2007, Vol. 22, pp. 2928-2935.
- Robertson S.A. and Sharkey D.J. Seminal fluid and fertility in women. Fertil. Steril., 2016, Vol. 106, no. 3, pp. 511-519.
- Sarno J.L., Schatz F., Lockwood C.J., Huang S.T., Taylor H.S. Thrombin and interleukin-1beta regulate HOXA10 expression in human term decidual cells: implications for preterm labor. J. Clin. Endocrinol. Metab., 2006, Vol. 91, no. 6, pp. 2366-2372.
- Sugama S. and Conti B. Interleukin-18 and stress. Brain Res. Rev., 2008, Vol. 58, no. 1, pp. 85-95.
- Tremellen K.P., Seamark R.F., Robertson S.A. Seminal transforming growth factor beta1 stimulates granulocyte-macrophage colony-stimulating factor production and inflammatory cell recruitment in the murine uterus. Biol. Reprod., 1998, Vol. 58, pp. 1217-1225.