Singapore Immunology Network (SIgN), A(∗)STAR, 8A Biomedical Grove, Immunos Building, Level 4, Singapore 138648, Singapore.
Translational Immunology Institute, Singhealth/Duke-NUS Academic Medical Centre, the Academia, 20 College Road, Discovery Tower Level 8, Singapore 169856, Singapore.
Cell. 2021 Jun 24;184(13):3394-3409.e20. doi: 10.1016/j.cell.2021.04.039. Epub 2021 Jun 1.
The human fetal immune system begins to develop early during gestation; however, factors responsible for fetal immune-priming remain elusive. We explored potential exposure to microbial agents in utero and their contribution toward activation of memory T cells in fetal tissues. We profiled microbes across fetal organs using 16S rRNA gene sequencing and detected low but consistent microbial signal in fetal gut, skin, placenta, and lungs in the 2 trimester of gestation. We identified several live bacterial strains including Staphylococcus and Lactobacillus in fetal tissues, which induced in vitro activation of memory T cells in fetal mesenteric lymph node, supporting the role of microbial exposure in fetal immune-priming. Finally, using SEM and RNA-ISH, we visualized discrete localization of bacteria-like structures and eubacterial-RNA within 14 weeks fetal gut lumen. These findings indicate selective presence of live microbes in fetal organs during the 2 trimester of gestation and have broader implications toward the establishment of immune competency and priming before birth.
人类胎儿的免疫系统在妊娠早期开始发育;然而,负责胎儿免疫启动的因素仍不清楚。我们探讨了胎儿期潜在的微生物暴露及其对胎儿组织中记忆 T 细胞激活的贡献。我们使用 16S rRNA 基因测序对胎儿器官中的微生物进行了分析,在妊娠中期的胎儿肠道、皮肤、胎盘和肺部中检测到低但一致的微生物信号。我们在胎儿组织中鉴定出了几种包括葡萄球菌和乳杆菌在内的活菌株,这些细菌株在体外诱导了胎儿肠系膜淋巴结中记忆 T 细胞的激活,支持了微生物暴露在胎儿免疫启动中的作用。最后,通过 SEM 和 RNA-ISH,我们在 14 周胎儿肠道腔中观察到了类似细菌结构和真核生物 RNA 的离散定位。这些发现表明,妊娠中期胎儿器官中存在活的微生物,这对出生前免疫能力的建立和启动具有更广泛的意义。