| Literature DB >> 30763769 |
Franca R Guerini1, Elisabetta Bolognesi2, Stefano Sotgiu3, Alessandra Carta4, Claudia Clerici2, Matteo Chiappedi5, Alessandro Ghezzo6, Michela Zanette2, Maria M Mensi5, Maria P Canevini7, Milena Zanzottera2, Cristina Agliardi2, Andrea S Costa2, Umberto Balottin8, Mario Clerici9.
Abstract
Recent results show that in mainland Italian children with Autism spectrum disorder (ASD), HLA-G coding alleles distribution is skewed and an association between HLA-G*01:05N and ASD is present. Herein, in an independent cohort of Sardinian ASD (sASD) children and their relatives, we verify whether HLA-G allele association with ASD could be confirmed in this genetically peculiar insular population. One hundred children with a diagnosis of ASD, born in Sardinia and of Sardinian descent, 91 of their mothers, and 40 of their healthy siblings were enrolled. DNA sequencing analysis of HLA-G exon 2, 3 and 4 was used to obtain HLA-G allelic frequencies. Alleles distribution was compared with that of continental ASD children and with a control group of Caucasoid couples of multiparous women and their partners from Brazil and Denmark. Skewing of HLA-G allele distribution was replicated in sASD children; in particular, the HLA-G*01:03 allele, associated with reduced fetal tolerogenicity and development of myeloid leukemia, was more common in both ASD groups compared to controls (pc = 1 × 10-3; OR:3.5, 95%CI: 1.8-6.8). However, given the lack of data on HLA-G*01:03 allelic distribution among Sardinian healthy subjects, we cannot exclude a population effect. These data confirm an association of HLA-G locus with ASD development, particularly with those alleles linked to a lower expression of tolerogenic HLA-G protein, thus warranting further studies on HLA-G polymorphism distribution in different ASD populations.Entities:
Keywords: Autistic spectrum disorder; Genetic polymorphism; HLA-G; Immune system; In utero immunology; KIR; NK cells
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Year: 2019 PMID: 30763769 DOI: 10.1016/j.bbi.2019.02.003
Source DB: PubMed Journal: Brain Behav Immun ISSN: 0889-1591 Impact factor: 7.217