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Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment?
Autism spectrum disorders (ASD) are characterized by impairments in language and communication development, social behavior, and the occurrence of stereotypic patterns of behavior and interests. Despite substantial speculation about causes of ASD, its exact etiology remains unknown. Recent studies h...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061181/ https://www.ncbi.nlm.nih.gov/pubmed/29307081 http://dx.doi.org/10.1007/s12035-017-0822-x |
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author | Gładysz, Dominika Krzywdzińska, Amanda Hozyasz, Kamil K. |
author_facet | Gładysz, Dominika Krzywdzińska, Amanda Hozyasz, Kamil K. |
author_sort | Gładysz, Dominika |
collection | PubMed |
description | Autism spectrum disorders (ASD) are characterized by impairments in language and communication development, social behavior, and the occurrence of stereotypic patterns of behavior and interests. Despite substantial speculation about causes of ASD, its exact etiology remains unknown. Recent studies highlight a link between immune dysfunction and behavioral traits. Various immune anomalies, including humoral and cellular immunity along with abnormalities at the molecular level, have been reported. There is evidence of altered immune function both in cerebrospinal fluid and peripheral blood. Several studies hypothesize a role for neuroinflammation in ASD and are supported by brain tissue and cerebrospinal fluid analysis, as well as evidence of microglial activation. It has been shown that immune abnormalities occur in a substantial number of individuals with ASD. Identifying subgroups with immune system dysregulation and linking specific cellular immunophenotypes to different symptoms would be key to defining a group of patients with immune abnormalities as a major etiology underlying behavioral symptoms. These determinations would provide the opportunity to investigate causative treatments for a defined patient group that may specifically benefit from such an approach. This review summarizes recent insights into immune system dysfunction in individuals with ASD and discusses the potential implications for future therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-017-0822-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6061181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-60611812018-08-09 Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? Gładysz, Dominika Krzywdzińska, Amanda Hozyasz, Kamil K. Mol Neurobiol Article Autism spectrum disorders (ASD) are characterized by impairments in language and communication development, social behavior, and the occurrence of stereotypic patterns of behavior and interests. Despite substantial speculation about causes of ASD, its exact etiology remains unknown. Recent studies highlight a link between immune dysfunction and behavioral traits. Various immune anomalies, including humoral and cellular immunity along with abnormalities at the molecular level, have been reported. There is evidence of altered immune function both in cerebrospinal fluid and peripheral blood. Several studies hypothesize a role for neuroinflammation in ASD and are supported by brain tissue and cerebrospinal fluid analysis, as well as evidence of microglial activation. It has been shown that immune abnormalities occur in a substantial number of individuals with ASD. Identifying subgroups with immune system dysregulation and linking specific cellular immunophenotypes to different symptoms would be key to defining a group of patients with immune abnormalities as a major etiology underlying behavioral symptoms. These determinations would provide the opportunity to investigate causative treatments for a defined patient group that may specifically benefit from such an approach. This review summarizes recent insights into immune system dysfunction in individuals with ASD and discusses the potential implications for future therapies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s12035-017-0822-x) contains supplementary material, which is available to authorized users. Springer US 2018-01-06 2018 /pmc/articles/PMC6061181/ /pubmed/29307081 http://dx.doi.org/10.1007/s12035-017-0822-x Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Article Gładysz, Dominika Krzywdzińska, Amanda Hozyasz, Kamil K. Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title | Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title_full | Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title_fullStr | Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title_full_unstemmed | Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title_short | Immune Abnormalities in Autism Spectrum Disorder—Could They Hold Promise for Causative Treatment? |
title_sort | immune abnormalities in autism spectrum disorder—could they hold promise for causative treatment? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6061181/ https://www.ncbi.nlm.nih.gov/pubmed/29307081 http://dx.doi.org/10.1007/s12035-017-0822-x |
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