PD‐1 mediates decidual γδ T cells cytotoxicity during recurrent pregnancy loss
Problem Recurrent pregnancy loss (RPL) is one of the big challenges of normal pregnancy. Immune dysregulation has been proposed for the key underline mechanisms of RPL. However, the essential roles of T cells, especially γδ T cells, have not been defined. Method of study Decidua were obtained from n...
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Veröffentlicht in: | American journal of reproductive immunology (1989) 2022-09, Vol.88 (3), p.e13562-n/a |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Problem
Recurrent pregnancy loss (RPL) is one of the big challenges of normal pregnancy. Immune dysregulation has been proposed for the key underline mechanisms of RPL. However, the essential roles of T cells, especially γδ T cells, have not been defined.
Method of study
Decidua were obtained from normal pregnancy women or recurrent pregnancy loss patients and the surface molecules of γδ T cells in decidua were evaluated via flow cytometric analysis. The expression of PD‐1 in clinical samples was analyzed by immunohistochemistry assay. The intracellular cytokines of decidual PD‐1+ and PD‐1‐ γδ T cells were evaluated by flow cytometric analysis. The cytotoxicity of PD‐1‐ γδ T cells were confirmed via an in vitro co‐culture experiment. The specific inhibitors for Erk, p38 and JNK against the MAPK pathway were added to the co‐culture media to evaluate the functions of the Erk, p38 and JNK.
Results
We demonstrated that PD‐1 was significantly decreased on decidual tissue γδ T cells of patients with RPL, resulting in the enhanced cytotoxicity of γδ T cells against trophoblasts. We further elucidated an Erk‐dependent TNF‐α production mediates the γδ T cell cytotoxicity against the trophoblast cells. Finally, the reduced expression of PD‐L1 in the villi tissues of patients with RPL might be the cause of the reduction of PD‐1 on the tissue γδ T cells.
Conclusion
Our study uncovers an important role of PD‐1 expression on decidual γδ T cells in maintaining the normal pregnancy, and may provide a new strategy for immune therapy against RPL. |
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ISSN: | 1046-7408 1600-0897 |
DOI: | 10.1111/aji.13562 |