Phenotypic characterization of human decidual macrophages

被引:219
作者
Heikkinen, J
Möttönen, M
Komi, J
Alanen, A
Lassila, O
机构
[1] Turku Univ, Dept Med Microbiol, Turku Grad Sch Biomed Sci, FIN-20520 Turku, Finland
[2] Turku Univ, Dept Obstet & Gynecol, FIN-20520 Turku, Finland
关键词
cytokines; decidual macrophages; IDO; phenotype;
D O I
10.1046/j.1365-2249.2003.02092.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pregnancy is a challenge to the immune system, which not only has to protect the mother and the fetus from invading pathogens but to also maintain immunological tolerance against the fetus. However, the mechanisms inhibiting local immune responses in the maternal decidual tissue are poorly understood. We have studied decidual CD14(+) macrophages, which may be important in the maintenance of a tolerance against the developing fetus. Decidual macrophages expressed HLA-DR, but lower levels of costimulatory molecule CD86 than peripheral blood CD14(+) monocytes from pregnant and non-pregnant women. Decidual macrophages produced spontaneously high levels of interleukin-10. Our findings suggest that decidual macrophages could represent an inhibitory type of APCs. Supporting this conclusion indoleamine 2,3-dioxygenase (IDO), suggested to have an immunosuppressive role in pregnancy, was expressed in decidual macrophages. Furthermore, decidual macrophages were not able to differentiate into dendritic cells under the influence of IL-4 + GM-CSF. These results suggest an immunoinhibitory function of decidual macrophages at the maternal-fetal interface.
引用
收藏
页码:498 / 505
页数:8
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