Immune-regulatory properties carried by human amnion epithelial cells: Focus on the role of HLA-G and adenosinergic ectoenzymes

被引:1
作者
Morandi, F. [1 ,6 ]
Airoldi, I. [1 ]
Faini, A. [2 ]
Horenstein, A. [2 ]
Malavasi, F. [2 ,3 ]
Matysiak, N. [4 ]
Kopaczka, K. [5 ]
Marimpietri, D. [1 ]
Gramignoli, R. [5 ]
机构
[1] IRCCS Ist Giannina Gaslini, UOSD Cell Factory, I-16147 Genoa, Italy
[2] Univ Torino, Dept Med Sci, Lab Immunogenet, I-10126 Turin, Italy
[3] Fdn Ric Molinette, Turin, Italy
[4] Med Univ Silesia, Dept Histol & Cell Pathol Zabrze, Katowice, Poland
[5] Karolinska Inst, Dept Lab Med, Div Pathol, SE-17177 Stockholm, Sweden
[6] IRCCS Ist Giannina Gaslini, UOSD Cell Factory, Via Gaslini 5, I-16147 Genoa, Italy
关键词
Amnion epithelial cells; Immune regulation; HLA-G; Adenosine; Ectonucleotidase; CLASS-I MOLECULES; STEM-CELLS; T-CELLS; EXPRESSION; ANTIGEN; MHC; IMMUNOGENICITY; TROPHOBLAST; RECEPTORS; MEMBRANE;
D O I
10.1016/j.humimm.2023.04.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human amnion epithelial cells (hAEC) can be efficiently isolated from full-term amnion membrane and have been gaining recognition as advanced medical products. Such cells originate directly from the embryo during the early phase of development and exert a crucial function in the establishment of a tolerogenic environment, to avoid maternal immune rejection. Amnion cell immuno-modulation may be exploited, but additional efforts are required to establish the mechanisms underlying such capacity. The way to fully clarify such an issue is so far long. Here we overview current knowledge on the effects on innate or adaptive immune cells offered by intact hAEC or secreted mediators, pinpointing the mechanisms to date elucidated by our group and others. We move from the description of hAEC general features to molecular intermediaries generating effects directly or indirectly on immune cells. We focus on the role of non-canonical HLA class I molecules, with emphasis on HLA-G, but expand such analysis on adenosinergic mediators, cytokines, and hAEC-derived microvesicles. Finally, we report the ongoing clinical trials exploiting hAEC multipotency and immune modulation.
引用
收藏
页码:359 / 365
页数:7
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