[The influence of chorionic gonadotropin on phenotype conversion and hTERT gene expression by T-lymphocytes of different degrees of differentiation].

The effects of chorionic gonadotropin (hCG) on the expression of the hTERT gene in combination with the conversion of the phenotype of naive T-cells and T-cells of immune memory in vitro were studied. hCG inhibited expression of hTERT mRNA in naive T-cells (CD45RA+) and immune memory T cells (CD45RO+), causing a decrease in the replicative potential of the cells. The presence of hCG in the culture led to the conversion of the phenotype of T-lymphocytes. hCG reduced the number of proliferating T-cells of immune memory, estimated by phenotypic signs by differential gating. hCG (10 IU/ml and 100 IU/ml) inhibited expression of CD25 by the studied populations, but did not modulate expression of the CD71 proliferation marker. Thus, hCG inhibited the functional activity of naive T-cells and T-cells of immune memory, which, in the context of pregnancy, can contribute to the formation of immune tolerance to the semi-allogenic fetus.

[1]  E. Orlova,et al.  [Apoptotic endonuclease EndoG regulates alternative splicing of human telomerase catalytic subunit hTERT]. , 2017, Biomeditsinskaia khimiia.

[2]  Philip D. Zisman,et al.  Overexpression of Telomerase Protects Human and Murine Lung Epithelial Cells from Fas- and Bleomycin-Induced Apoptosis via FLIP Upregulation , 2015, PloS one.

[3]  A. Zenclussen,et al.  Human Chorionic Gonadotropin as a Central Regulator of Pregnancy Immune Tolerance , 2013, The Journal of Immunology.

[4]  A. Benko,et al.  Estrogen and telomerase in human peripheral blood mononuclear cells , 2012, Molecular and Cellular Endocrinology.

[5]  M. Shipkova,et al.  Surface markers of lymphocyte activation and markers of cell proliferation. , 2012, Clinica chimica acta; international journal of clinical chemistry.

[6]  L. Cole hCG, the wonder of today's science , 2012, Reproductive Biology and Endocrinology.

[7]  E. Barsov Telomerase and primary T cells: biology and immortalization for adoptive immunotherapy. , 2011, Immunotherapy.

[8]  I. Sargent,et al.  Systemic Inflammatory Priming in Normal Pregnancy and Preeclampsia: The Role of Circulating Syncytiotrophoblast Microparticles1 , 2007, The Journal of Immunology.

[9]  N. Bache,et al.  Protein Composition of Catalytically Active Human Telomerase from Immortal Cells , 2007, Science.

[10]  K. Ohtani,et al.  Identification of two distinct elements mediating activation of telomerase (hTERT) gene expression in association with cell growth in human T cells. , 2004, International immunology.

[11]  Antonio Lanzavecchia,et al.  Central memory and effector memory T cell subsets: function, generation, and maintenance. , 2004, Annual review of immunology.

[12]  F. Sallusto,et al.  Proliferation and differentiation potential of human CD8+ memory T-cell subsets in response to antigen or homeostatic cytokines. , 2003, Blood.

[13]  Thomas D. Schmittgen,et al.  Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. , 2001, Methods.

[14]  R. Hockett,et al.  Interleukin-2 expression by a subpopulation of primary T cells is linked to enhanced memory/effector function. , 1999, Immunity.

[15]  H. Macdonald,et al.  Light scatter analysis and sorting of cells activated in mixed leukocyte culture. , 1982, Cytometry.

[16]  D. Santi,et al.  Clinical Applications of Gonadotropins in the Female: Assisted Reproduction and Beyond. , 2016, Progress in molecular biology and translational science.

[17]  M. Trněný,et al.  The evaluation of survival and proliferation of lymphocytes in autologous mixed leukocyte reaction with dendritic cells. The comparison of incorporation of (3)H-thymidine and differential gating method. , 2011, Cellular immunology.

[18]  A. Akbar,et al.  Memory T cell homeostasis and senescence during aging. , 2005, Current opinion in immunology.