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Anti-TPO-mediated specific features of the placenta immunohistochemical profile and possible mechanisms for fetal loss. / Borodina, Elena; Gzgzyan, Alexander M; Dzhemlikhanova, Liailia Kh; Niauri, Dariko A; Tolibova, Gulrukhsor Kh; Tral, Tatiana G; Kogan, Igor Y; Safarian, Galina Kh; Ostrinski, Yuri; Churilov, Leonid P; Amital, Howard; Blank, Miri; Shoenfeld, Yehuda.

In: Clinical and Experimental Immunology, Vol. 213, No. 2, 21.07.2023, p. 235-242.

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Borodina, E, Gzgzyan, AM, Dzhemlikhanova, LK, Niauri, DA, Tolibova, GK, Tral, TG, Kogan, IY, Safarian, GK, Ostrinski, Y, Churilov, LP, Amital, H, Blank, M & Shoenfeld, Y 2023, 'Anti-TPO-mediated specific features of the placenta immunohistochemical profile and possible mechanisms for fetal loss', Clinical and Experimental Immunology, vol. 213, no. 2, pp. 235-242. https://doi.org/10.1093/cei/uxad057

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Author

Borodina, Elena ; Gzgzyan, Alexander M ; Dzhemlikhanova, Liailia Kh ; Niauri, Dariko A ; Tolibova, Gulrukhsor Kh ; Tral, Tatiana G ; Kogan, Igor Y ; Safarian, Galina Kh ; Ostrinski, Yuri ; Churilov, Leonid P ; Amital, Howard ; Blank, Miri ; Shoenfeld, Yehuda. / Anti-TPO-mediated specific features of the placenta immunohistochemical profile and possible mechanisms for fetal loss. In: Clinical and Experimental Immunology. 2023 ; Vol. 213, No. 2. pp. 235-242.

BibTeX

@article{0f2e8a62c32940acaef58adf72c0f9ae,
title = "Anti-TPO-mediated specific features of the placenta immunohistochemical profile and possible mechanisms for fetal loss",
abstract = "Passive transfer of antithyroid antibodies in mice leads to reproductive disorders. The purpose was to assess the placental tissue of experimental animals under the influence of the circulating thyroperoxidase antibodies. We performed an immunohistochemical examination of murine placentae after a passive transfer of thyroperoxidase antibodies. Placentae of mice that passively transferred IgG from healthy donors were used as control samples. For histological examination, 30 placental samples were selected from mice from the anti-TPO group and 40 placental samples were taken from mice from the IgG group. Immunostaining for VEGFR1, THBS 1, Laminin, CD31, CD34, FGF-β, CD56, CD14, TNF-α, kisspeptin, MCL 1, and Annexin V was performed. There is a significant decrease in the relative area of the expression of VEGFR1 (23.42 ± 0.85 vs. 33.44 ± 0.35, P < 0.01), thrombospondin 1 (31.29 ± 0.83 vs. 34.51 ± 0.75, P < 0.01), CD14 (25.80 ± 0.57 vs. 32.07 ± 0.36, P < .01), CD56 (30.08 ± 0.90 vs. 34.92 ± 0.15, P < 0.01), kisspeptin (25.94 ± 0.47 vs. 31.27 ± 0.57, P < 0.01), MCL 1 (29.24 ± 1.06 vs. 38.57 ± 0.79, P < 0.01) in the labyrinth zone of the placentae of mice from the anti-TPO group compared with control group. A significant increase in the relative expression of laminin and FGF-β was noted in the group of mice to which antibodies to thyroperoxidase were transferred, compared with the control group (36.73 ± 1.38 vs. 29.83 ± 0.94, P < 0.01 and 23.26 ± 0.61 vs. 16.38 ± 1.01, P < 0.01respectively). Our study exposed an imbalance of pro- and anti-angiogenic factors, decreased representation of placental macrophages and NK cells, abnormal trophoblast invasion processes, and insufficient expression of antiapoptotic factors in the placentae of mice in which anti-TPO antibodies were passively transferred.",
keywords = "Pregnancy, Female, Animals, Mice, Placenta/pathology, Laminin/metabolism, Kisspeptins/metabolism, Myeloid Cell Leukemia Sequence 1 Protein/metabolism, Immunoglobulin G/metabolism",
author = "Elena Borodina and Gzgzyan, {Alexander M} and Dzhemlikhanova, {Liailia Kh} and Niauri, {Dariko A} and Tolibova, {Gulrukhsor Kh} and Tral, {Tatiana G} and Kogan, {Igor Y} and Safarian, {Galina Kh} and Yuri Ostrinski and Churilov, {Leonid P} and Howard Amital and Miri Blank and Yehuda Shoenfeld",
note = "{\textcopyright} The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Immunology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.",
year = "2023",
month = jul,
day = "21",
doi = "10.1093/cei/uxad057",
language = "English",
volume = "213",
pages = "235--242",
journal = "Clinical and Experimental Immunology",
issn = "0009-9104",
publisher = "Wiley-Blackwell",
number = "2",

}

RIS

TY - JOUR

T1 - Anti-TPO-mediated specific features of the placenta immunohistochemical profile and possible mechanisms for fetal loss

AU - Borodina, Elena

AU - Gzgzyan, Alexander M

AU - Dzhemlikhanova, Liailia Kh

AU - Niauri, Dariko A

AU - Tolibova, Gulrukhsor Kh

AU - Tral, Tatiana G

AU - Kogan, Igor Y

AU - Safarian, Galina Kh

AU - Ostrinski, Yuri

AU - Churilov, Leonid P

AU - Amital, Howard

AU - Blank, Miri

AU - Shoenfeld, Yehuda

N1 - © The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Immunology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

PY - 2023/7/21

Y1 - 2023/7/21

N2 - Passive transfer of antithyroid antibodies in mice leads to reproductive disorders. The purpose was to assess the placental tissue of experimental animals under the influence of the circulating thyroperoxidase antibodies. We performed an immunohistochemical examination of murine placentae after a passive transfer of thyroperoxidase antibodies. Placentae of mice that passively transferred IgG from healthy donors were used as control samples. For histological examination, 30 placental samples were selected from mice from the anti-TPO group and 40 placental samples were taken from mice from the IgG group. Immunostaining for VEGFR1, THBS 1, Laminin, CD31, CD34, FGF-β, CD56, CD14, TNF-α, kisspeptin, MCL 1, and Annexin V was performed. There is a significant decrease in the relative area of the expression of VEGFR1 (23.42 ± 0.85 vs. 33.44 ± 0.35, P < 0.01), thrombospondin 1 (31.29 ± 0.83 vs. 34.51 ± 0.75, P < 0.01), CD14 (25.80 ± 0.57 vs. 32.07 ± 0.36, P < .01), CD56 (30.08 ± 0.90 vs. 34.92 ± 0.15, P < 0.01), kisspeptin (25.94 ± 0.47 vs. 31.27 ± 0.57, P < 0.01), MCL 1 (29.24 ± 1.06 vs. 38.57 ± 0.79, P < 0.01) in the labyrinth zone of the placentae of mice from the anti-TPO group compared with control group. A significant increase in the relative expression of laminin and FGF-β was noted in the group of mice to which antibodies to thyroperoxidase were transferred, compared with the control group (36.73 ± 1.38 vs. 29.83 ± 0.94, P < 0.01 and 23.26 ± 0.61 vs. 16.38 ± 1.01, P < 0.01respectively). Our study exposed an imbalance of pro- and anti-angiogenic factors, decreased representation of placental macrophages and NK cells, abnormal trophoblast invasion processes, and insufficient expression of antiapoptotic factors in the placentae of mice in which anti-TPO antibodies were passively transferred.

AB - Passive transfer of antithyroid antibodies in mice leads to reproductive disorders. The purpose was to assess the placental tissue of experimental animals under the influence of the circulating thyroperoxidase antibodies. We performed an immunohistochemical examination of murine placentae after a passive transfer of thyroperoxidase antibodies. Placentae of mice that passively transferred IgG from healthy donors were used as control samples. For histological examination, 30 placental samples were selected from mice from the anti-TPO group and 40 placental samples were taken from mice from the IgG group. Immunostaining for VEGFR1, THBS 1, Laminin, CD31, CD34, FGF-β, CD56, CD14, TNF-α, kisspeptin, MCL 1, and Annexin V was performed. There is a significant decrease in the relative area of the expression of VEGFR1 (23.42 ± 0.85 vs. 33.44 ± 0.35, P < 0.01), thrombospondin 1 (31.29 ± 0.83 vs. 34.51 ± 0.75, P < 0.01), CD14 (25.80 ± 0.57 vs. 32.07 ± 0.36, P < .01), CD56 (30.08 ± 0.90 vs. 34.92 ± 0.15, P < 0.01), kisspeptin (25.94 ± 0.47 vs. 31.27 ± 0.57, P < 0.01), MCL 1 (29.24 ± 1.06 vs. 38.57 ± 0.79, P < 0.01) in the labyrinth zone of the placentae of mice from the anti-TPO group compared with control group. A significant increase in the relative expression of laminin and FGF-β was noted in the group of mice to which antibodies to thyroperoxidase were transferred, compared with the control group (36.73 ± 1.38 vs. 29.83 ± 0.94, P < 0.01 and 23.26 ± 0.61 vs. 16.38 ± 1.01, P < 0.01respectively). Our study exposed an imbalance of pro- and anti-angiogenic factors, decreased representation of placental macrophages and NK cells, abnormal trophoblast invasion processes, and insufficient expression of antiapoptotic factors in the placentae of mice in which anti-TPO antibodies were passively transferred.

KW - Pregnancy

KW - Female

KW - Animals

KW - Mice

KW - Placenta/pathology

KW - Laminin/metabolism

KW - Kisspeptins/metabolism

KW - Myeloid Cell Leukemia Sequence 1 Protein/metabolism

KW - Immunoglobulin G/metabolism

U2 - 10.1093/cei/uxad057

DO - 10.1093/cei/uxad057

M3 - Article

C2 - 37243348

VL - 213

SP - 235

EP - 242

JO - Clinical and Experimental Immunology

JF - Clinical and Experimental Immunology

SN - 0009-9104

IS - 2

ER -

ID: 129847716