Mizobuchi Haruka, Yamagishi Junya, Sanjoba Chizu, Goto Yasuyuki
Laboratory of Molecular Immunology, Department of Animal Resource Sciences, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo, Japan.
International Collaboration Unit, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
PLoS Negl Trop Dis. 2025 Jun 9;19(6):e0012650. doi: 10.1371/journal.pntd.0012650. eCollection 2025 Jun.
Visceral leishmaniasis (VL) is a zoonotic disease caused by infection of macrophages by Leishmania donovani or L. infantum, and exhibits symptoms such as fever, anemia, and hepatosplenomegaly. VL during pregnancy has been reported to have negative effects such as miscarriage and vertical infection, but the mechanism is not clear. Here, we aimed to establish a pregnant VL mouse model and elucidate its immunopathology. Female BALB/c mice mated 6 months after L. donovani infection showed reduced pregnancy rates. The fetus was removed by caesarean section on the 18th day of pregnancy, and Leishmania parasite DNA was detected from fetal spleens and livers. As a result, the PCR positive rate was 68.9% (71/103 fetus), and vertical transmission was suspected in 66.7% of infected mothers (12/18 dams). Immunohistochemistry in the fetal livers detected cells positive for the Leishmania antigen, kinetoplastid membrane protein 11 (KMP11). In addition, pathological analysis of the VL placenta revealed trophoblast cell atrophy and vasodilation accompanied by CD3+ cell infiltration in the infected group. On the other hand, few KMP11+ cells were observed in the placenta of the infected group. Furthermore, RNA-Seq analysis revealed that IFN signal activation and cellular immune suppression were induced in the placenta of the infected group. These results suggest that VL in pregnancy induces suppression of placental cellular immunity through IFN and collapse of the placental barrier through trophoblast degeneration, leading to vertical transmission. Because few infected macrophages were observed in the placenta, it is possible that free Leishmania parasites in the blood contribute to transmission across the placenta.
内脏利什曼病(VL)是一种人畜共患病,由杜氏利什曼原虫或婴儿利什曼原虫感染巨噬细胞引起,表现出发热、贫血和肝脾肿大等症状。据报道,妊娠期VL会产生如流产和垂直感染等负面影响,但其机制尚不清楚。在此,我们旨在建立妊娠VL小鼠模型并阐明其免疫病理学。感染杜氏利什曼原虫6个月后交配的雌性BALB/c小鼠妊娠率降低。在妊娠第18天通过剖腹产取出胎儿,从胎儿脾脏和肝脏中检测到利什曼原虫DNA。结果,PCR阳性率为68.9%(71/103个胎儿),66.7%的感染母亲(12/18只母鼠)疑似发生垂直传播。胎儿肝脏的免疫组织化学检测到利什曼原虫抗原动质体膜蛋白11(KMP11)阳性的细胞。此外,VL胎盘的病理分析显示,感染组存在滋养层细胞萎缩和血管扩张,并伴有CD3+细胞浸润。另一方面,在感染组的胎盘中观察到很少的KMP11+细胞。此外,RNA测序分析显示,感染组胎盘诱导了IFN信号激活和细胞免疫抑制。这些结果表明,妊娠期VL通过IFN诱导胎盘细胞免疫抑制,并通过滋养层变性导致胎盘屏障破坏,从而导致垂直传播。由于在胎盘中观察到的感染巨噬细胞很少,血液中的游离利什曼原虫可能有助于跨胎盘传播。