Cross-Talk between Mucosal-Associated Invariant T, Natural Killer, and Natural Killer T Cell Populations is Implicated in the Pathogenesis of Placenta Accreta Spectrum

被引:1
|
作者
El-Badawy, Omnia [1 ]
Abbas, Ahmed M. [2 ]
Radwan, Eman [3 ,4 ]
Makboul, Rania [5 ]
Khamis, Areej A. [2 ]
Ali, Maha [3 ]
Elkabsh, Mai M. [5 ]
Bakr, Marwa H. [6 ]
Zahran, Asmaa M. [7 ]
机构
[1] Assiut Univ, Fac Med, Dept Med Microbiol & Immunol, Assiut 71515, Egypt
[2] Assiut Univ, Fac Med, Obstet & Gynecol Dept, Assiut, Egypt
[3] Assiut Univ, Fac Med, Dept Med Biochem, Assiut, Egypt
[4] Sphinx Univ, Dept Biochem, Assiut, Egypt
[5] Assiut Univ, Fac Med, Pathol Dept, Assiut, Egypt
[6] Assiut Univ, Fac Med, Dept Histol & Cell Biol, Assiut, Egypt
[7] Assiut Univ, South Egypt Canc Inst, Dept Clin Pathol, Assiut, Egypt
关键词
MAIT; NK cells; NKT cells; placenta accreta spectrum; VEGF; ENG; sFLT-1; NKT CELLS; TISSUE-REPAIR; GRANZYME-B; MAIT CELLS; TGF-BETA; IN-VIVO; ACTIVATION; INVASION; TCR; CYTOTOXICITY;
D O I
10.1007/s10753-023-01799-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The study included 32 women with PAS and 20 with normally implanted placenta as a control group. Vascular endothelial cell growth factor (VEGF), Soluble FMS Like Tyrosine Kinase (sFLT-1/sVEGFR1), and Endoglin (ENG) were measured in placenta tissue by ELISA. Granzyme B (GrzB) expression in trophoblastic and stromal mesenchymal cells was evaluated by immunohistochemistry. MAIT, NK, and NKT cells were assessed in blood and placenta by flow cytometry. Alterations were observed in levels of MAIT cells, NK cell subsets, and NKT cells in patients compared with controls. Several significant correlations were detected between these cells and GrzB scores, VEGF, ENG, and sFLT-1 levels. This is the first study analysing these cells in PAS patients and correlating their levels with changes in some angiogenic and antiangiogenic factors implicated in trophoblast invasion and with GrzB distribution in trophoblast and stroma. Interrelation between these cells probably plays an important role in pathogenesis of PAS.
引用
收藏
页码:1192 / 1208
页数:17
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