Ji-Xu Antonio, Vincent Angela
NHS Foundation Trust, Oxford University Hospitals, Oxford OX3 9DU, UK.
Nuffield Department of Clinical Neurosciences and MRC, Weatherall Institute of Molecular Medicine, Oxford OX3 9DU, UK.
J Clin Med. 2020 Aug 10;9(8):2590. doi: 10.3390/jcm9082590.
Autism spectrum disorders (ASD) are complex neurodevelopmental disorders with unknown heterogeneous aetiologies. Epidemiological studies have found an association between maternal infection and development of ASD in the offspring, and clinical findings reveal a state of immune dysregulation in the pre- and postnatal period of affected subjects. Maternal immune activation (MIA) has been proposed to mediate this association by altering fetal neurodevelopment and leading to autism. Although animal models have supported a causal link between MIA and development of ASD, their validity needs to be explored. Moreover, considering that only a small proportion of affected offspring develop autism, and that MIA has been implicated in related diseases such as schizophrenia, a key unsolved question is how disease specificity and phenotypic outcome are determined. Here, we have integrated preclinical and clinical evidence, including the use of animal models for establishing causality, to explore the role of maternal infections in ASD. A proposed priming/multi-hit model may offer insights into the clinical heterogeneity of ASD, its convergence with related disorders, and therapeutic strategies.
自闭症谱系障碍(ASD)是病因不明且异质性的复杂神经发育障碍。流行病学研究发现,母亲感染与后代ASD的发生之间存在关联,临床研究结果显示,受影响个体在产前和产后存在免疫失调状态。有人提出,母体免疫激活(MIA)通过改变胎儿神经发育并导致自闭症来介导这种关联。尽管动物模型支持MIA与ASD发生之间存在因果关系,但其有效性仍需探索。此外,鉴于只有一小部分受影响的后代会患自闭症,而且MIA与精神分裂症等相关疾病有关,一个关键的未解决问题是疾病特异性和表型结果是如何确定的。在这里,我们整合了临床前和临床证据,包括使用动物模型来确定因果关系,以探讨母体感染在ASD中的作用。提出的启动/多重打击模型可能为ASD的临床异质性、与相关疾病的趋同性以及治疗策略提供见解。