Doyle-Meyers Lara, Dong Chunming, Xu Eddie Qidi, Vallender Eric J, Blair Robert V, Didier Peter, He Fenglei, Wang Xiaolei
Division of Veterinary Medicine, Tulane National Primate Research Center, 18703 Three Rivers Road, Covington, LA, 70433, USA.
Department of Cell and Molecular Biology, School of Science and Engineering, Tulane University, 6823 St. Charles Avenue, New Orleans, LA, 70118, USA.
Curr Trends Immunol. 2023;24:91-103.
Cyclopia, a rare genetic anomaly and birth defect, was recently observed in our nonhuman primate study. A newborn rhesus macaque, delivered cesarean section, exhibited facial abnormalities, including a single eye in the middle of the forehead. This macaque was born to a dam who had been inoculated with SIV in the first trimester and received antiretroviral therapy (ART) in the early third trimester of pregnancy. Prenatal ultrasound detected fetal defects, including the fusion of the thalami and absence of third ventricle during the third trimester of fetal development. Remarkably, the newborn macaque was diagnosed with severe alobar holoprosencephaly, characterized by a single eye located on the facial midline and proboscises positioned above and below the eye. This condition was accompanied by the absence of a nose, mouth, mandible, maxilla, nasal and oral cavities, tongue, as well as the esophagus. Subsequent genetic screening identified a significant down-regulation of craniofacial development-associated genes, although genetic mutations in the sonic hedgehog gene () were not present. As the fetal defects were identified prior to the initiation of antiretroviral therapy, it is possible that other environmental factors may have contributed to the development of cyclopia in this rhesus case. However, the etiology of this congenital HPE case remains essentially unknown.
独眼畸形是一种罕见的基因异常和出生缺陷,最近在我们的非人灵长类动物研究中被观察到。一只通过剖宫产出生的新生恒河猴表现出面部异常,包括前额中央有一只眼睛。这只猕猴的母亲在孕早期接种了猴免疫缺陷病毒(SIV),并在妊娠晚期接受了抗逆转录病毒治疗(ART)。产前超声在胎儿发育晚期检测到胎儿缺陷,包括丘脑融合和第三脑室缺失。值得注意的是,这只新生猕猴被诊断为重度无脑叶全前脑畸形,其特征是面部中线有一只眼睛,眼睛上下有长鼻。这种情况还伴有鼻子、嘴巴、下颌骨、上颌骨、鼻腔和口腔、舌头以及食管缺失。随后的基因筛查发现颅面发育相关基因显著下调,尽管没有发现音猬因子基因()的基因突变。由于在开始抗逆转录病毒治疗之前就已发现胎儿缺陷,因此在这只恒河猴病例中,其他环境因素可能导致了独眼畸形的发生。然而,这例先天性全前脑畸形病例的病因基本上仍不清楚。