Arenella Martina, Matuleviciute Rugile, Tamouza Ryad, Leboyer Marion, McAlonan Grainne, Bralten Janita, Murphy Declan
Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands; Donders Institute of Brain, Cognition and Behavior, Radboud University, Nijmegen, The Netherlands.
Department of Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, London, United Kingdom.
Brain Behav Immun. 2023 Nov;114:488-499. doi: 10.1016/j.bbi.2023.09.010. Epub 2023 Sep 16.
The aetiology of autism spectrum disorder (ASD) is complex and, partly, accounted by genetic factors. Nonetheless, the genetic underpinnings of ASD are poorly defined. The presence of immune dysregulations in autistic individuals, and their families, supports a role of the immune system and its genetic regulators. Albeit immune responses belong either to the innate or adaptive arms, the overall immune system genetics is broad, and encompasses a multitude of functionally heterogenous pathways which may have different influences on ASD. Hence, to gain insights on the immunogenetic underpinnings of ASD, we conducted a systematic literature review of previous immune genetic and transcription studies in ASD. We defined a list of immune genes relevant to ASD and explored their neuro-immune function. Our review confirms the presence of immunogenetic variability in ASD, accounted by inherited variations of innate and adaptive immune system genes and genetic expression changes in the blood and post-mortem brain of autistic individuals. Besides their immune function, the identified genes control neurodevelopment processes (neuronal and synaptic plasticity) and are highly expressed in pre/peri-natal periods. Hence, our synthesis bolsters the hypothesis that perturbation in immune genes may contribute to ASD by derailing the typical trajectory of neurodevelopment. Our review also helped identifying some of the limitations of prior immunogenetic research in ASD. Thus, alongside clarifying the neurodevelopment role of immune genes, we outline key considerations for future work into the aetiology of ASD and possible novel intervention targets.
自闭症谱系障碍(ASD)的病因复杂,部分由遗传因素所致。尽管如此,ASD的遗传基础仍未明确。自闭症个体及其家庭成员中存在免疫失调现象,这支持了免疫系统及其遗传调节因子的作用。虽然免疫反应属于先天性或适应性免疫,但整体免疫遗传学范畴广泛,涵盖众多功能各异的途径,这些途径可能对ASD产生不同影响。因此,为深入了解ASD的免疫遗传学基础,我们对先前关于ASD的免疫遗传学和转录研究进行了系统的文献综述。我们确定了与ASD相关的免疫基因列表,并探讨了它们的神经免疫功能。我们的综述证实了ASD中存在免疫遗传变异性,这是由先天性和适应性免疫系统基因的遗传变异以及自闭症个体血液和死后大脑中的基因表达变化所致。除了免疫功能外,所确定的基因还控制神经发育过程(神经元和突触可塑性),并在产前/围产期高度表达。因此,我们的综合研究支持了这样一种假设,即免疫基因的扰动可能通过扰乱神经发育的典型轨迹而导致ASD。我们的综述还有助于识别先前ASD免疫遗传学研究的一些局限性。因此,在阐明免疫基因的神经发育作用的同时,我们概述了未来ASD病因研究的关键考虑因素以及可能的新干预靶点。