Immune checkpoints TIM-3 and Gal-9 are upregulated in male placentas with acute SARS-CoV-2 infection

New data indicate an increased risk of obstetric complications after Covid-19, the aim of this study was therefore to investigate the expression of immune checkpoint molecules TIM-3 and Gal-9 in tissue sections of placenta from patients with acute Covid-19, from patients after Covid-19 infection and from healthy controls. We used a total of 60 placentas from women who had given birth to female or male children at Augsburg University Hospital, Germany. We examined 10 placentas each with acute Covid-19 from female and male fetuses, 10 placentas each from female and male fetuses after acute Covid-19 and 10 placentas each from female and male fetuses of a healthy control group. Immunohistochemical staining against TIM-3 and Gal-9 was performed, and marker expression was assessed by an immunoreactive score (IRS). The identity of cells expressing TIM-3 or Gal-9 was then analyzed by double immunofluorescence analysis. TIM-3- and Gal-9 positive macrophages are significantly upregulated in the decidua of female acute Covid-19 placentas. TIM-3 is significantly up-regulated in male extravillous trophoblast cells in the acute phase of Covid-19. On the other hand, TIM-3 was significantly downregulated in Hofbauer cells from male placentas after Covid-19. Gal-9, the ligand for TIM-3, was significantly downregulated in Hofbauer cells from male placentas after Covid-19. Triple immunofluorescence analysis showed that male acute Covid-19 Hofbauer cells (analyzed by CD163 staining) were positive for both TIM-3 and Gal-9. Surprisingly, the observed effects were related to fetal sex. In particular, the formative effect of this infection needs to be analyzed in further studies.

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Publication Details

Journal
Journal of Reproductive Immunology
Published
2025-10-28
DOI
https://doi.org/10.1016/j.jri.2025.104797
Primary Topic
Complement system in diseases
Type
article
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article

Immune checkpoints TIM-3 and Gal-9 are upregulated in male placentas with acute SARS-CoV-2 infection

Marei Sammar, Christian Dannecker, Nina Ditsch, Marina Seefried et al.
Journal of Reproductive Immunology
Complement system in diseases
article

Immune checkpoints TIM-3 and Gal-9 are upregulated in male placentas with acute SARS-CoV-2 infection

Marei Sammar, Christian Dannecker, Nina Ditsch, Marina Seefried, Carl Mathis Wild, Christina Kühn, Johanna Mittelberger, Udo Jeschke, Britta C. Urban, Peter Altevogt, Manuela Franitza, Jonas Bubmann, Ines Lurtz
article en

Abstract

New data indicate an increased risk of obstetric complications after Covid-19, the aim of this study was therefore to investigate the expression of immune checkpoint molecules TIM-3 and Gal-9 in tissue sections of placenta from patients with acute Covid-19, from patients after Covid-19 infection and from healthy controls. We used a total of 60 placentas from women who had given birth to female or male children at Augsburg University Hospital, Germany. We examined 10 placentas each with acute Covid-19 from female and male fetuses, 10 placentas each from female and male fetuses after acute Covid-19 and 10 placentas each from female and male fetuses of a healthy control group. Immunohistochemical staining against TIM-3 and Gal-9 was performed, and marker expression was assessed by an immunoreactive score (IRS). The identity of cells expressing TIM-3 or Gal-9 was then analyzed by double immunofluorescence analysis. TIM-3- and Gal-9 positive macrophages are significantly upregulated in the decidua of female acute Covid-19 placentas. TIM-3 is significantly up-regulated in male extravillous trophoblast cells in the acute phase of Covid-19. On the other hand, TIM-3 was significantly downregulated in Hofbauer cells from male placentas after Covid-19. Gal-9, the ligand for TIM-3, was significantly downregulated in Hofbauer cells from male placentas after Covid-19. Triple immunofluorescence analysis showed that male acute Covid-19 Hofbauer cells (analyzed by CD163 staining) were positive for both TIM-3 and Gal-9. Surprisingly, the observed effects were related to fetal sex. In particular, the formative effect of this infection needs to be analyzed in further studies.

Journal of Reproductive ImmunologyVol. 172
University of Augsburg (DE), Heidelberg University (DE), Braude College of Engineering Karmiel (IL), University Hospital Augsburg (DE), University Hospital Heidelberg (DE), University Medical Centre Mannheim (DE)
Openalex Percentile: Top 68%
Complement system in diseases
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