Immunogenetics of autism spectrum disorder: A systematic literature review

被引:11
作者
Arenella, Martina [1 ,2 ,3 ]
Matuleviciute, Rugile [4 ,5 ]
Tamouza, Ryad [6 ,7 ]
Leboyer, Marion [6 ,7 ]
Mcalonan, Grainne [1 ,8 ]
Bralten, Janita [2 ,3 ]
Murphy, Declan [1 ,8 ]
机构
[1] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Forens & Neurodev Sci, London, England
[2] Radboud Univ Nijmegen Med Ctr, Dept Human Genet, Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[4] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Basic & Clin Neurosci, London, England
[5] Kings Coll London, MRC Ctr Neurodev Disorders, London, England
[6] Univ Paris Est Creteil UPEC, Dept Addict & Psychiat DMU IMPACT, Translat Neuropsychiat Lab, INSERM,IMRB,AP HP,DMU IMPACT,FHU ADAPT, Creteil, France
[7] Fdn FondaMental, F-94010 Creteil, France
[8] South London & Maudsley NHS Fdn Trust, London, England
基金
英国医学研究理事会;
关键词
MATERNAL IMMUNE ACTIVATION; BRAIN-DEVELOPMENT; AUTOIMMUNE-DISEASES; LIFE-SPAN; HLA-G; ASSOCIATION; PREGNANCY; CYTOKINES; CHILDREN; POLYMORPHISMS;
D O I
10.1016/j.bbi.2023.09.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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/perinatal 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.
引用
收藏
页码:488 / 499
页数:12
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