The placenta utilizes many mechanisms to protect the haploidentical fetus from recognition by the maternal immune system. However, in cases of villitis of unknown etiology (VUE), maternal lymphocytes gain access into the placenta, causing significant health risks for the fetus. Evidence suggests that VUE is a rejection response between the mother and the haploidentical fetus. Therefore, we profiled human leukocyte antigen (HLA), an important predictor of transplant rejection, in VUE using placental tissue from ten patients with VUE and ten gestational age matched controls. Placentas were stained using novel multiplexed immunofluorescence (MxIF) to investigate morphology and HLA classes I and II. Gene expression was evaluated by microarray, and where available, tissue typing of mother/baby pairs was completed to determine HLA type. MxIF demonstrated strong CD8+ T cell infiltration and HLA class I staining both the distal and stem villi of VUE placentas. Compared to controls, VUE cases had significantly higher expression of HLA class II mRNA and pathway analysis demonstrated that 40% of the differentially expressed genes in VUE are related to tissue rejection. The data suggest that VUE resembles a rejection response between the mother and the fetus. It remains unknown what initiates immune recognition and why some mothers appear to be at higher risk for developing this condition than others. Understanding this etiology will be critical for developing effective interventions or prevention strategies during pregnancy.
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Hop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Hop Mondor, Inst Mondor Rech Biomed, INSERM U955, Creteil, France
Hop Albert Chenevier, Fdn Fondamental, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Bennabi, M.
Delorme, R.
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Hop Robert Debre, AP HP, Serv Psychiat Enfant & Adolescent, DHU Protect, Paris, France
Inst Pasteur, Dept Genet Humaine & Fonct Cognit, Paris, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Delorme, R.
Oliveira, J.
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Hop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Hop Mondor, Inst Mondor Rech Biomed, INSERM U955, Creteil, France
Hop Albert Chenevier, Fdn Fondamental, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Oliveira, J.
Boukouaci, W.
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Hop St Louis, Inst Univ Hematol, INSERM U1160, Paris, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Boukouaci, W.
Gaman, A.
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Hop Mondor, Inst Mondor Rech Biomed, INSERM U955, Creteil, France
Hop Albert Chenevier, Fdn Fondamental, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Gaman, A.
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Charron, D.
Ghaleh, B.
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Hop Univ Henri Mondor, Ctr Ressources Biol, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Ghaleh, B.
Krishnamoorthy, R.
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Hop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Hop Albert Chenevier, Fdn Fondamental, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Krishnamoorthy, R.
Leboyer, M.
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Hop Mondor, Inst Mondor Rech Biomed, INSERM U955, Creteil, France
Hop Albert Chenevier, Fdn Fondamental, Creteil, France
Univ Paris Est Creteil, Fac Med, Creteil, France
Hop Univ Henri Mondor, AP HP, DHU PePSY, Pole Psychiat, Creteil, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France
Leboyer, M.
Tamouza, R.
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Hop Albert Chenevier, Fdn Fondamental, Creteil, France
Hop St Louis, Lab Jean Dausset, Paris, France
Hop St Louis, LabEx Transplantex, Paris, France
Univ Paris Diderot, Sorbonne Paris Cite, Paris, FranceHop St Louis, Inst Univ Hematol, INSERM U1160, Paris, France