Innate immune defenses at the maternal-fetal interface

被引:28
作者
Semmes, Eleanor C. [1 ,2 ,3 ]
Coyne, Carolyn B. [2 ,3 ]
机构
[1] Duke Univ, Med Scientist Training Program, Durham, NC USA
[2] Duke Univ, Mol Genet & Microbiol Dept, Durham, NC 27706 USA
[3] Duke Univ, Duke Human Vaccine Inst, Durham, NC 27706 USA
关键词
CELLS; TROPHOBLASTS; INTERFERONS; INFECTION;
D O I
10.1016/j.coi.2021.10.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human maternal-fetal interface is an immunologically complex environment that must balance the divergent demands of tolerance towards the developing fetus with anti-pathogen defense. The innate immune responses at the maternal-fetal interface that function in anti-microbial defense have been understudied to-date and how 'TORCH' pathogens evade maternal innate immunity to infect the fetus remains poorly understood. Herein, we discuss how newly described decidual innate lymphoid cells and maternal placenta-associated macrophage subsets may be involved in anti-pathogen defense. Moreover, we outline recent advances in our understanding of how placental trophoblasts and fetal-derived macrophages (Hofbauer cells) function in anti-microbial defense. In summary, we highlight current gaps in knowledge and describe novel experimental models of the human decidua and placenta that are poised to advance our knowledge of innate immune defenses at the maternal-fetal interface.
引用
收藏
页码:60 / 67
页数:8
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